Name

AMLCR2 Gene

acute myeloid leukemia chromosome region 2

MLRL Gene

Myeloid leukemia-related gene (myeloid tumor suppressor)

MDS2 Gene

myelodysplastic syndrome 2 translocation associated

BLM Gene

Bloom syndrome, RecQ helicase-like

The Bloom syndrome gene product is related to the RecQ subset of DExH box-containing DNA helicases and has both DNA-stimulated ATPase and ATP-dependent DNA helicase activities. Mutations causing Bloom syndrome delete or alter helicase motifs and may disable the 3'-5' helicase activity. The normal protein may act to suppress inappropriate recombination. [provided by RefSeq, Jul 2008]

LALL Gene

Lymphomatous acute lymphoblastic leukemia

ALL2 Gene

Leukemia, acute lymphoblastic, susceptibility to, 2

TAL1 Gene

T-cell acute lymphocytic leukemia 1

TAL2 Gene

T-cell acute lymphocytic leukemia 2

This intronless gene encodes a helix-loop-helix protein. Translocations between this gene on chromosome 9 and the T-cell receptor beta-chain locus on chromosome 7 have been associated with activation of the T-cell acute lymphocytic leukemia 2 gene and T-cell acute lymphoblastic leukemia. [provided by RefSeq, Mar 2009]

ALL1 Gene

Leukemia, acute lymphocytic, susceptibility to, 1

BLACE Gene

B-cell acute lymphoblastic leukemia expressed

BAALC Gene

brain and acute leukemia, cytoplasmic

This gene was identified by gene expression studies in patients with acute myeloid leukemia (AML). The gene is conserved among mammals and is not found in lower organisms. Tissues that express this gene develop from the neuroectoderm. Multiple alternatively spliced transcript variants that encode different proteins have been described for this gene; however, some of the transcript variants are found only in AML cell lines. [provided by RefSeq, Jul 2008]

MCL1 Gene

myeloid cell leukemia 1

This gene encodes an anti-apoptotic protein, which is a member of the Bcl-2 family. Alternative splicing results in multiple transcript variants. The longest gene product (isoform 1) enhances cell survival by inhibiting apoptosis while the alternatively spliced shorter gene products (isoform 2 and isoform 3) promote apoptosis and are death-inducing. [provided by RefSeq, Oct 2010]

LOC100419977 Gene

myeloid leukemia factor 2 pseudogene

MLLT10P1 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 pseudogene 1

MLF1 Gene

myeloid leukemia factor 1

This gene encodes an oncoprotein which is thought to play a role in the phenotypic determination of hemopoetic cells. Translocations between this gene and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]

MLF2 Gene

myeloid leukemia factor 2

MLLT10 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10

This gene encodes a transcription factor and has been identified as a partner gene involved in several chromosomal rearrangements resulting in various leukemias. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010]

MLLT11 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 11

The gene variously symbolized ALL1, HRX, or MLL located on 11q23 has been demonstrated to be fused with a number of translocation partners in cases of leukemia. t(1;11)(q21;q23) translocations that fused the MLL gene to a gene on chromosomal band 1q21 in 2 infants with acute myelomonocytic leukemia have been demonstrated. The N-terminal portion of the MLL gene is critical for leukemogenesis in translocations involving band 11q23. This gene encodes 90 amino acids. It was found to be highly expressed in the thymus but not in peripheral lymphoid tissues. In contrast to its restricted distribution in normal hematopoietic tissue, this gene was expressed in all leukemic cell lines tested. [provided by RefSeq, Jul 2008]

MLLT4 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 4

This gene encodes a multi-domain protein involved in signaling and organization of cell junctions during embryogenesis. It has also been identified as the fusion partner of acute lymphoblastic leukemia (ALL-1) gene, involved in acute myeloid leukemias with t(6;11)(q27;q23) translocation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, however, not all have been fully characterized.[provided by RefSeq, May 2011]

MLLT6 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 6

MLLT1 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 1

MLLT3 Gene

myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3

LOC105375109 Gene

skin secretory protein xP2-like

PI3 Gene

peptidase inhibitor 3, skin-derived

This gene encodes an elastase-specific inhibitor that functions as an antimicrobial peptide against Gram-positive and Gram-negative bacteria, and fungal pathogens. The protein contains a WAP-type four-disulfide core (WFDC) domain, and is thus a member of the WFDC domain family. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. Expression of this gene is upgulated by bacterial lipopolysaccharides and cytokines. [provided by RefSeq, Oct 2014]

LOC105379200 Gene

skin secretory protein xP2-like

TST2 Gene

Tuberculin skin test reactivity QTL

TST1 Gene

Tuberculin skin test reactivity, absence of

LOC105374086 Gene

skin secretory protein xP2-like

SHEP8 Gene

Skin/hair/eye pigmentation 8, freckling

KWE Gene

keratolytic winter erythema (Oudtshoorn skin disease)

LOC105378948 Gene

skin secretory protein xP2-like

MLSM7 Gene

Myelodysplasia and leukemia syndrome with monosomy 7

STARP1 Gene

steroidogenic acute regulatory protein pseudogene 1

AIR Gene

Acute insulin response (2)

STAR Gene

steroidogenic acute regulatory protein

The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jul 2008]

STAT3 Gene

signal transducer and activator of transcription 3 (acute-phase response factor)

The protein encoded by this gene is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated through phosphorylation in response to various cytokines and growth factors including IFNs, EGF, IL5, IL6, HGF, LIF and BMP2. This protein mediates the expression of a variety of genes in response to cell stimuli, and thus plays a key role in many cellular processes such as cell growth and apoptosis. The small GTPase Rac1 has been shown to bind and regulate the activity of this protein. PIAS3 protein is a specific inhibitor of this protein. Three alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]

MYDGF Gene

myeloid-derived growth factor

The protein encoded by this gene was previously thought to support proliferation of lymphoid cells and was considered an interleukin. However, this activity has not been reproducible and the function of this protein is currently unknown. [provided by RefSeq, Jul 2008]

MYADML2 Gene

myeloid-associated differentiation marker-like 2

MNDA Gene

myeloid cell nuclear differentiation antigen

The myeloid cell nuclear differentiation antigen (MNDA) is detected only in nuclei of cells of the granulocyte-monocyte lineage. A 200-amino acid region of human MNDA is strikingly similar to a region in the proteins encoded by a family of interferon-inducible mouse genes, designated Ifi-201, Ifi-202, and Ifi-203, that are not regulated in a cell- or tissue-specific fashion. The 1.8-kb MNDA mRNA, which contains an interferon-stimulated response element in the 5-prime untranslated region, was significantly upregulated in human monocytes exposed to interferon alpha. MNDA is located within 2,200 kb of FCER1A, APCS, CRP, and SPTA1. In its pattern of expression and/or regulation, MNDA resembles IFI16, suggesting that these genes participate in blood cell-specific responses to interferons. [provided by RefSeq, Jul 2008]

TREML3P Gene

triggering receptor expressed on myeloid cells-like 3, pseudogene

TREML3 is located in a gene cluster on chromosome 6 with the single Ig variable (IgV) domain activating receptors TREM1 (MIM 605085) and TREM2 (MIM 605086), but it has distinct structural and functional properties (Allcock et al., 2003 [PubMed 12645956]).[supplied by OMIM, Mar 2008]

HOTAIRM1 Gene

HOXA transcript antisense RNA, myeloid-specific 1

This non-coding locus is located in the HOX gene cluster. Transcription of this locus is induced by retinoic acid, and transcripts likely function in regulation of myelopoiesis through transcriptional activation of several genes in the HOXA cluster, in addition to several beta-2 integrins. [provided by RefSeq, Jan 2013]

MYADM Gene

myeloid-associated differentiation marker

TREML5P Gene

triggering receptor expressed on myeloid cells-like 5, pseudogene

FUT4 Gene

fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific)

The product of this gene transfers fucose to N-acetyllactosamine polysaccharides to generate fucosylated carbohydrate structures. It catalyzes the synthesis of the non-sialylated antigen, Lewis x (CD15). [provided by RefSeq, Jan 2009]

MZF1 Gene

myeloid zinc finger 1

LOC105375057 Gene

triggering receptor expressed on myeloid cells 1-like

TREML2 Gene

triggering receptor expressed on myeloid cells-like 2

TREML2 is located in a gene cluster on chromosome 6 with the single Ig variable (IgV) domain activating receptors TREM1 (MIM 605085) and TREM2 (MIM 605086), but it has distinct structural and functional properties (Allcock et al., 2003 [PubMed 12645956]).[supplied by OMIM, Mar 2008]

TREML1 Gene

triggering receptor expressed on myeloid cells-like 1

This gene encodes a member of the triggering receptor expressed on myeloid cells-like (TREM) family. The encoded protein is a type 1 single Ig domain orphan receptor localized to the alpha-granule membranes of platelets. The encoded protein is involved in platelet aggregation, inflammation, and cellular activation and has been linked to Gray platelet syndrome. Alternative splicing results in multiple transcript variants [provided by RefSeq, Nov 2012]

TREML4 Gene

triggering receptor expressed on myeloid cells-like 4

MYD88 Gene

myeloid differentiation primary response 88

This gene encodes a cytosolic adapter protein that plays a central role in the innate and adaptive immune response. This protein functions as an essential signal transducer in the interleukin-1 and Toll-like receptor signaling pathways. These pathways regulate that activation of numerous proinflammatory genes. The encoded protein consists of an N-terminal death domain and a C-terminal Toll-interleukin1 receptor domain. Patients with defects in this gene have an increased susceptibility to pyogenic bacterial infections. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

TREM1 Gene

triggering receptor expressed on myeloid cells 1

This gene encodes a receptor belonging to the Ig superfamily that is expressed on myeloid cells. This protein amplifies neutrophil and monocyte-mediated inflammatory responses triggered by bacterial and fungal infections by stimulating release of pro-inflammatory chemokines and cytokines, as well as increased surface expression of cell activation markers. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jun 2011]

TREM2 Gene

triggering receptor expressed on myeloid cells 2

This gene encodes a membrane protein that forms a receptor signaling complex with the TYRO protein tyrosine kinase binding protein. The encoded protein functions in immune response and may be involved in chronic inflammation by triggering the production of constitutive inflammatory cytokines. Defects in this gene are a cause of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2012]

MYADML Gene

myeloid-associated differentiation marker-like (pseudogene)

TARM1 Gene

T cell-interacting, activating receptor on myeloid cells 1

DGS2 Gene

DiGeorge syndrome/velocardiofacial syndrome complex 2

LIF Gene

leukemia inhibitory factor

The protein encoded by this gene is a pleiotropic cytokine with roles in several different systems. It is involved in the induction of hematopoietic differentiation in normal and myeloid leukemia cells, induction of neuronal cell differentiation, regulator of mesenchymal to epithelial conversion during kidney development, and may also have a role in immune tolerance at the maternal-fetal interface. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]

TSL Gene

testis-expressed, seven-twelve, leukemia

TCTA Gene

T-cell leukemia translocation altered

TCL6 Gene

T-cell leukemia/lymphoma 6 (non-protein coding)

TCL4 Gene

T-cell leukemia/lymphoma 4

LYL1 Gene

lymphoblastic leukemia associated hematopoiesis regulator 1

This gene represents a basic helix-loop-helix transcription factor. The encoded protein may play roles in blood vessel maturation and hematopoeisis. A translocation between this locus and the T cell receptor beta locus (GeneID 6957) on chromosome 7 has been associated with acute lymphoblastic leukemia. [provided by RefSeq, Sep 2010]

CLLS1 Gene

Leukemia, chronic lymphocytic, susceptibility to, 1

CLLS5 Gene

Leukemia, chronic lymphocytic susceptiblity to, 5

LOC402641 Gene

v-ral simian leukemia viral oncogene homolog A (ras related) pseudogene

FLVCR2 Gene

feline leukemia virus subgroup C cellular receptor family, member 2

This gene encodes a member of the major facilitator superfamily. The encoded transmembrane protein is a calcium transporter. Unlike the related protein feline leukemia virus subgroup C receptor 1, the protein encoded by this locus does not bind to feline leukemia virus subgroup C envelope protein. The encoded protein may play a role in development of brain vascular endothelial cells, as mutations at this locus have been associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome. Alternatively spliced transcript variants have been described.[provided by RefSeq, Aug 2010]

FLVCR1 Gene

feline leukemia virus subgroup C cellular receptor 1

This gene encodes a member of the major facilitator superfamily of transporter proteins. The encoded protein is a heme transporter that may play a critical role in erythropoiesis by protecting developing erythroid cells from heme toxicity. This gene may play a role in posterior column ataxia with retinitis pigmentosa and the hematological disorder Diamond-Blackfan syndrome. [provided by RefSeq, Jan 2011]

PBXIP1 Gene

pre-B-cell leukemia homeobox interacting protein 1

CLLS3 Gene

Leukemia, chronic lymphocytic, susceptibility to, 3

RALB Gene

v-ral simian leukemia viral oncogene homolog B

This gene encodes a GTP-binding protein that belongs to the small GTPase superfamily and Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. [provided by RefSeq, Jul 2008]

RALA Gene

v-ral simian leukemia viral oncogene homolog A (ras related)

The product of this gene belongs to the small GTPase superfamily, Ras family of proteins. GTP-binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. This gene encodes a low molecular mass ras-like GTP-binding protein that shares about 50% similarity with other ras proteins. [provided by RefSeq, Jul 2008]

CLLU1OS Gene

chronic lymphocytic leukemia up-regulated 1 opposite strand

SSAV1 Gene

simian sarcoma-associated virus 1/gibbon ape leukemia virus-related endogenous retroviral element 1

DLEU2L Gene

deleted in lymphocytic leukemia 2-like

HLFP1 Gene

hepatic leukemia factor pseudogene 1

FIM3 Gene

Friend-murine leukemia virus integration site 3 homolog

CLLU1 Gene

chronic lymphocytic leukemia up-regulated 1

PBX4 Gene

pre-B-cell leukemia homeobox 4

This gene encodes a member of the pre-B cell leukemia transcription factor family. These proteins are homeobox proteins that play critical roles in embryonic development and cellular differentiation both as Hox cofactors and through Hox-independent pathways. The encoded protein contains a homeobox DNA-binding domain, but specific functions of the protein have not been determined. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2011]

PBX2 Gene

pre-B-cell leukemia homeobox 2

This gene encodes a ubiquitously expressed member of the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]

PBX3 Gene

pre-B-cell leukemia homeobox 3

PBX1 Gene

pre-B-cell leukemia homeobox 1

This gene encodes a nuclear protein that belongs to the PBX homeobox family of transcriptional factors. Studies in mice suggest that this gene may be involved in the regulation of osteogenesis, and required for skeletal patterning and programming. A chromosomal translocation, t(1;19) involving this gene and TCF3/E2A gene, is associated with pre-B-cell acute lymphoblastic leukemia. The resulting fusion protein, in which the DNA binding domain of E2A is replaced by the DNA binding domain of this protein, transforms cells by constitutively activating transcription of genes regulated by the PBX protein family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]

TAX1BP1 Gene

Tax1 (human T-cell leukemia virus type I) binding protein 1

This gene encodes a HTLV-1 tax1 binding protein. The encoded protein interacts with TNFAIP3, and inhibits TNF-induced apoptosis by mediating the TNFAIP3 anti-apoptotic activity. Degradation of this protein by caspase-3-like family proteins is associated with apoptosis induced by TNF. This protein may also have a role in the inhibition of inflammatory signaling pathways. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]

TAX1BP3 Gene

Tax1 (human T-cell leukemia virus type I) binding protein 3

FIM1 Gene

Friend-murine leukemia virus integration site 1 homolog

LUNAR1 Gene

leukemia-associated non-coding IGF1R activator RNA 1

This gene is thought to produce a functional long non-coding RNA. It is regulated by Notch and is overexpressed in T cell acute lymphoblastic leukemia. The transcript acts as a positive regulator of cell division by promoting expression of the insulin-like growth factor type I receptor (IGF1R) gene. [provided by RefSeq, Feb 2015]

CLLS4 Gene

Leukemia, chronic lymphocytic susceptibility to, 4

LOC642550 Gene

v-ral simian leukemia viral oncogene homolog A (ras related) pseudogene

PBX2P1 Gene

pre-B-cell leukemia homeobox 2 pseudogene 1

TLX1 Gene

T-cell leukemia homeobox 1

This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily of homeobox genes. The encoded protein is required for normal development of the spleen during embryogenesis. This protein is also involved in specification of neuronal cell fates. Ectopic expression of this gene due to chromosomal translocations is associated with certain T-cell acute lymphoblastic leukemias. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]

TLX2 Gene

T-cell leukemia homeobox 2

This gene is a member of an orphan homeobox-containing transcription factor family. Studies of the mouse ortholog have shown that the encoded protein is crucial for the development of the enteric nervous system; in humans, loss-of-function may play a role in tumorigenesis of gastrointestinal stromal tumors. [provided by RefSeq, May 2010]

TLX3 Gene

T-cell leukemia homeobox 3

RNX (HOX11L2, TLX3) belongs to a family of orphan homeobox genes that encode DNA-binding nuclear transcription factors. Members of the HOX11 gene family are characterized by a threonine-47 replacing cytosine in the highly conserved homeodomain (Dear et al., 1993 [PubMed 8099440]).[supplied by OMIM, Mar 2008]

PML Gene

promyelocytic leukemia

The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This phosphoprotein localizes to nuclear bodies where it functions as a transcription factor and tumor suppressor. Its expression is cell-cycle related and it regulates the p53 response to oncogenic signals. The gene is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL). Extensive alternative splicing of this gene results in several variations of the protein's central and C-terminal regions; all variants encode the same N-terminus. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

TCL1B Gene

T-cell leukemia/lymphoma 1B

TCL1A Gene

T-cell leukemia/lymphoma 1A

Overexpression of the TCL1 gene in humans has been implicated in the development of mature T cell leukemia, in which chromosomal rearrangements bring the TCL1 gene in close proximity to the T-cell antigen receptor (TCR)-alpha (MIM 186880) or TCR-beta (MIM 186930) regulatory elements (summarized by Virgilio et al., 1998 [PubMed 9520462]). In normal T cells TCL1 is expressed in CD4-/CD8- cells, but not in cells at later stages of differentiation. TCL1 functions as a coactivator of the cell survival kinase AKT (MIM 164730) (Laine et al., 2000 [PubMed 10983986]).[supplied by OMIM, Jul 2010]

LNP1 Gene

leukemia NUP98 fusion partner 1

HLF Gene

hepatic leukemia factor

This gene encodes a member of the proline and acidic-rich (PAR) protein family, a subset of the bZIP transcription factors. The encoded protein forms homodimers or heterodimers with other PAR family members and binds sequence-specific promoter elements to activate transcription. Chromosomal translocations fusing portions of this gene with the E2A gene cause a subset of childhood B-lineage acute lymphoid leukemias. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]

TFPT Gene

TCF3 (E2A) fusion partner (in childhood Leukemia)

LIFR Gene

leukemia inhibitory factor receptor alpha

This gene encodes a protein that belongs to the type I cytokine receptor family. This protein combines with a high-affinity converter subunit, gp130, to form a receptor complex that mediates the action of the leukemia inhibitory factor, a polyfunctional cytokine that is involved in cellular differentiation, proliferation and survival in the adult and the embryo. Mutations in this gene cause Schwartz-Jampel syndrome type 2, a disease belonging to the group of the bent-bone dysplasias. A translocation that involves the promoter of this gene, t(5;8)(p13;q12) with the pleiomorphic adenoma gene 1, is associated with salivary gland pleiomorphic adenoma, a common type of benign epithelial tumor of the salivary gland. Multiple splice variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

MLVI2 Gene

Moloney murine leukemia virus (MoMuLV) integration site 2 homolog

MLVI4 Gene

Moloney leukemia virus integration site 4, mouse, homolog of

DLEU2 Gene

deleted in lymphocytic leukemia 2 (non-protein coding)

DLEU1 Gene

deleted in lymphocytic leukemia 1 (non-protein coding)

DLEU7 Gene

deleted in lymphocytic leukemia, 7

MKL1 Gene

megakaryoblastic leukemia (translocation) 1

The protein encoded by this gene interacts with the transcription factor myocardin, a key regulator of smooth muscle cell differentiation. The encoded protein is predominantly nuclear and may help transduce signals from the cytoskeleton to the nucleus. This gene is involved in a specific translocation event that creates a fusion of this gene and the RNA-binding motif protein-15 gene. This translocation has been associated with acute megakaryocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

MAGEH1 Gene

melanoma antigen family H1

This gene belongs to the non-CT (non cancer/testis) subgroup of the melanoma-associated antigen (MAGE) superfamily. The encoded protein is likely associated with apoptosis, cell cycle arrest, growth inhibition or cell differentiation. The protein may be involved in the atRA (all-trans retinoic acid) signaling through the STAT1-alpha (signal transducer and activator of transcription 1-alpha) pathway. [provided by RefSeq, Aug 2013]

MAGEL2 Gene

melanoma antigen family L2

Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]

CMM Gene

cutaneous malignant melanoma/dysplastic nevus

Malignant melanoma is a malignant neoplasm of melanocytes, arising de novo or from a pre-existing benign nevus, which occurs most often in the skin but also may involve other sites.[supplied by OMIM, Jul 2002]

MAGED4B Gene

melanoma antigen family D4B

This gene is a member of the MAGED gene family. It is expressed only in brain and ovary, and some transcript variants of this gene are specifically expressed in glioma cells. This gene is clustered with other MAGED genes on chromosome Xp11. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2011]

LOC100420250 Gene

melanoma antigen family A4 pseudogene

MAGEA7P Gene

melanoma antigen family A7, pseudogene

MAGEE2 Gene

melanoma antigen family E2

This gene encodes a member of the E subfamily of MAGE (melanoma antigen-encoding gene) gene family. The gene is intronless and the encoded protein has two of the MAGE domains which are characteristic of MAGE family proteins. [provided by RefSeq, Sep 2011]

MAGEE1 Gene

melanoma antigen family E1

This gene encodes an alpha-dystrobrevin-associated MAGE (melanoma-associated antigen) protein, which is a member of the MAGE family. The protein contains a nuclear localization signal in the N-terminus, 30 12-amino acid repeats beginning at nt 60 with the consensus sequence ASEGPSTSVLPT, and two MAGE domains in the C-terminus. It may play a signaling role in brain, muscle, and peripheral nerve. This gene is located on X chromosome in a region containing loci linked to mental retardation. [provided by RefSeq, Mar 2010]

MCAM Gene

melanoma cell adhesion molecule

LOC392435 Gene

melanoma antigen family B3 pseudogene

LOC392436 Gene

melanoma antigen family B4 pseudogene

LOC728307 Gene

melanoma associated antigen (mutated) 1-like 1 pseudogene

LOC100420318 Gene

melanoma antigen family A, 12 pseudogene

MAGEA2B Gene

melanoma antigen family A2B

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. [provided by RefSeq, Jul 2008]

LOC100420331 Gene

melanoma antigen family A10 pseudogene

LOC100420334 Gene

melanoma antigen family A11 pseudogene

MAGEF1 Gene

melanoma antigen family F1

This intronless gene encodes a member of the MAGE superfamily. It is ubiquitously expressed in normal tissues and in tumor cells. This gene includes a microsatellite repeat in the coding region. [provided by RefSeq, Jul 2008]

MAGEA11 Gene

melanoma antigen family A11

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

MIA3 Gene

melanoma inhibitory activity family, member 3

MAGEB17 Gene

melanoma antigen family B17

BAGE Gene

B melanoma antigen

This gene encodes a tumor antigen recognized by autologous cytolytic lymphocytes (CTL). [provided by RefSeq, Jul 2008]

PRAME Gene

preferentially expressed antigen in melanoma

This gene encodes an antigen that is preferentially expressed in human melanomas and that is recognized by cytolytic T lymphocytes. It is not expressed in normal tissues, except testis. The encoded protein acts as a repressor of retinoic acid receptor, and likely confers a growth advantage to cancer cells via this function. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]

MAGEA9B Gene

melanoma antigen family A9B

MAGEA9B is a duplication of the MAGEA9 gene (MIM 300342) on chromosome Xq28. The 2 copies are separated by about 194 kb (Hartz, 2009).[supplied by OMIM, Mar 2009]

MAGEA12 Gene

melanoma antigen family A12

This gene is closely related to several other genes clustered on chromosome X. These genes may be overexpressed in tumors. Multiple alternatively spliced variants encoding the same protein have been identified. [provided by RefSeq, Jun 2014]

MAGEA10 Gene

melanoma antigen family A10

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream melanoma antigen family A, 5 (MAGEA5) gene.[provided by RefSeq, Oct 2011]

AIM1L Gene

absent in melanoma 1-like

CMM4 Gene

Melanoma, cutaneous malignant, 4

MAGEC1 Gene

melanoma antigen family C1

This gene is a member of the melanoma antigen gene (MAGE) family. The proteins of this family are tumor-specific antigens that can be recognized by autologous cytolytic T lymphocytes. This protein contains a large number of unique short repetitive sequences in front of the MAGE-homologous sequence, and therefore is about 800 aa longer than the other MAGE proteins. [provided by RefSeq, Jul 2008]

MAGEC3 Gene

melanoma antigen family C3

This gene is a member of the MAGEC gene family. The members of this family are not expressed in normal tissues, except for testis, and are expressed in tumors of various histological types. The MAGEC genes are clustered on chromosome Xq26-q27. Two transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

MAGEC2 Gene

melanoma antigen family C2

This gene is a member of the MAGEC gene family. It is not expressed in normal tissues, except for testis, and is expressed in tumors of various histological types. This gene and the other MAGEC genes are clustered on chromosome Xq26-q27. [provided by RefSeq, Oct 2009]

LOC100533669 Gene

melanoma antigen family A10 pseudogene

MUM1 Gene

melanoma associated antigen (mutated) 1

LOC644893 Gene

melanoma antigen family E1 pseudogene

LOC100420228 Gene

melanoma antigen family C3 pseudogene

LOC101927262 Gene

melanoma-associated antigen C1-like

LOC392555 Gene

melanoma antigen family C2 pseudogene

MAGED1 Gene

melanoma antigen family D1

This gene is a member of the melanoma antigen gene (MAGE) family. Most of the genes of this family encode tumor specific antigens that are not expressed in normal adult tissues except testis. Although the protein encoded by this gene shares strong homology with members of the MAGE family, it is expressed in almost all normal adult tissues. This gene has been demonstrated to be involved in the p75 neurotrophin receptor mediated programmed cell death pathway. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

MAGED2 Gene

melanoma antigen family D2

This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked mental retardation (XLMR). This gene may also be involved in several types of cancer, including breast cancer and melanoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

MAGED4 Gene

melanoma antigen family D4

CMM7 Gene

Melanoma, cutaneous malignant, susceptibility to, 7

MIA2 Gene

melanoma inhibitory activity 2

CXCL1 Gene

chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha)

This antimicrobial gene encodes a member of the CXC subfamily of chemokines. The encoded protein is a secreted growth factor that signals through the G-protein coupled receptor, CXC receptor 2. This protein plays a role in inflammation and as a chemoattractant for neutrophils. Aberrant expression of this protein is associated with the growth and progression of certain tumors. A naturally occurring processed form of this protein has increased chemotactic activity. Alternate splicing results in coding and non-coding variants of this gene. A pseudogene of this gene is found on chromosome 4. [provided by RefSeq, Sep 2014]

LOC100420322 Gene

melanoma antigen family A10 pseudogene

LOC100420324 Gene

melanoma antigen family A10 pseudogene

LOC100420321 Gene

melanoma antigen family A11 pseudogene

LOC100420323 Gene

melanoma antigen family B18 pseudogene

LOC100420325 Gene

melanoma antigen family B16 pseudogene

BA255A11.4 Gene

melanoma antigen pseudogene

MAGEA9 Gene

melanoma antigen family A9

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]

MAGEA8 Gene

melanoma antigen family A8

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2009]

MAGEA3 Gene

melanoma antigen family A3

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]

MAGEA2 Gene

melanoma antigen family A2

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This gene has two identical copies at different loci. Alternatively spliced transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]

MAGEA1 Gene

melanoma antigen family A1

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]

MAGEA6 Gene

melanoma antigen family A6

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

MAGEA5 Gene

melanoma antigen family A5

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. This MAGEA gene encodes a protein that is C-terminally truncated compared to other family members, and this gene can be alternatively interpreted to be a pseudogene. The protein is represented in this Gene record in accordance with the assumed protein-coding status defined in the literature. Read-through transcription exists between this gene and the upstream melanoma antigen family A, 10 (MAGEA10) gene. [provided by RefSeq, Oct 2011]

MAGEA4 Gene

melanoma antigen family A4

This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. At least four variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

MAGEB18 Gene

melanoma antigen family B18

MAGEB10 Gene

melanoma antigen family B10

This gene encodes a member of the B subfamily of the melanoma associated antigen protein family. The encoded protein is specifically expressed in testis and tumor cells. [provided by RefSeq, Apr 2010]

MAGEB16 Gene

melanoma antigen family B16

MEAT6 Gene

melanoma-associated transcript 6

LOC100420249 Gene

melanoma antigen family C, 3 pseudogene

LOC100420245 Gene

melanoma antigen family B3 pseudogene

PSMAGEA Gene

melanoma antigen family A4 pseudogene

MUM1L1 Gene

melanoma associated antigen (mutated) 1-like 1

This gene encodes a protein which contains a mutated melanoma-associated antigen 1 domain. Proteins which contain mutated antigens are expressed at high levels on certain types of cancers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]

MAGEB2 Gene

melanoma antigen family B2

This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region. It is expressed in testis and placenta, and in a significant fraction of tumors of various histological types. The MAGEB genes are clustered on chromosome Xp22-p21. [provided by RefSeq, Jul 2008]

MAGEB3 Gene

melanoma antigen family B3

This gene is a MAGE-B subfamily member of the MAGE gene family. MAGE family member proteins direct the expression of tumor antigens recognized on a human melanoma by autologous cytolytic T lymphocytes. There are two known clusters of MAGE genes on chromosome X. The members of the MAGE-A subfamily are located in the Xq28 region, while the members of the MAGE-B subfamily are clustered in the Xp21 region. [provided by RefSeq, Jul 2008]

MAGEB1 Gene

melanoma antigen family B1

This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is localized in the DSS (dosage-sensitive sex reversal) critical region, and expressed in testis and in a significant fraction of tumors of various histological types. This gene and other MAGEB members are clustered on chromosome Xp22-p21. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene, however, the full length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]

MAGEB6 Gene

melanoma antigen family B6

This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. This gene is expressed in testis, and in a significant fraction of tumors of various histological types. The MAGEB genes are clustered on chromosome Xp22-p21. [provided by RefSeq, Jul 2008]

MAGEB4 Gene

melanoma antigen family B4

This gene is a member of the MAGEB gene family. The members of this family have their entire coding sequences located in the last exon, and the encoded proteins show 50 to 68% sequence identity to each other. The promoters and first exons of the MAGEB genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEB genes are clustered on chromosome Xp22-p21. This gene sequence ends in the first intron of MAGEB1, another family member. This gene is expressed in testis. [provided by RefSeq, Jul 2008]

MAGEB5 Gene

melanoma antigen family B5

LOC392440 Gene

melanoma antigen family B18 pseudogene

MIA Gene

melanoma inhibitory activity

LOC100130052 Gene

melanoma antigen family B3 pseudogene

UVM2 Gene

Melanoma, uveal, susceptibility to, 2

UVM1 Gene

Melanoma, uveal, susceptibility to, 1

LOC100420230 Gene

melanoma antigen family C3 pseudogene

LOC728317 Gene

melanoma associated antigen (mutated) 1-like 1 pseudogene

LOC100419702 Gene

necdin, melanoma antigen (MAGE) family member pseudogene

MAGEA13P Gene

melanoma antigen family A13, pseudogene

AIM1 Gene

absent in melanoma 1

AIM2 Gene

absent in melanoma 2

AIM2 is a member of the IFI20X /IFI16 family. It plays a putative role in tumorigenic reversion and may control cell proliferation. Interferon-gamma induces expression of AIM2. [provided by RefSeq, Jul 2008]

NDN Gene

necdin, melanoma antigen (MAGE) family member

This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]

MFI2 Gene

antigen p97 (melanoma associated) identified by monoclonal antibodies 133.2 and 96.5

The protein encoded by this gene is a cell-surface glycoprotein found on melanoma cells. The protein shares sequence similarity and iron-binding properties with members of the transferrin superfamily. The importance of the iron binding function has not yet been identified. This gene resides in the same region of chromosome 3 as members of the transferrin superfamily. Alternative splicing results in two transcript variants. [provided by RefSeq, Jul 2008]

MAGEB6P1 Gene

melanoma antigen family B6 pseudogene 1

BAGE4 Gene

B melanoma antigen family, member 4

BAGE5 Gene

B melanoma antigen family, member 5

BAGE2 Gene

B melanoma antigen family, member 2

BAGE3 Gene

B melanoma antigen family, member 3

TCOF1 Gene

Treacher Collins-Franceschetti syndrome 1

This gene encodes a nucleolar protein with a LIS1 homology domain. The protein is involved in ribosomal DNA gene transcription through its interaction with upstream binding factor (UBF). Mutations in this gene have been associated with Treacher Collins syndrome, a disorder which includes abnormal craniofacial development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008]

CDAGS Gene

Craniosynostosis, anal anomalies, and porokeratosis syndrome

PISRT1 Gene

polled intersex syndrome regulated transcript 1 (non-protein coding RNA)

SPG21 Gene

spastic paraplegia 21 (autosomal recessive, Mast syndrome)

The protein encoded by this gene binds to the hydrophobic C-terminal amino acids of CD4 which are involved in repression of T cell activation. The interaction with CD4 is mediated by the noncatalytic alpha/beta hydrolase fold domain of this protein. It is thus proposed that this gene product modulates the stimulatory activity of CD4. Mutations in this gene are associated with autosomal recessive spastic paraplegia 21 (SPG21), also known as mast syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]

FRIASS Gene

Frias syndrome

DEL8Q13 Gene

Mesomelia-synostoses syndrome

RENS2 Gene

Renpenning syndrome 2

DUP5P13 Gene

Chromosome 5p13 duplication syndrome

USH3B Gene

Usher syndrome 3B

ASPG2 Gene

Asperger syndrome, susceptibility to, 2

ASPG3 Gene

Asperger syndrome, susceptibility to, 3

ASPG4 Gene

Asperger syndrome, susceptibility to, 4

MGS Gene

Mungan syndrome

FWS Gene

Forsythe-Wakeling syndrome

DEL15Q26QTER Gene

Chromosome 15q26-qter deletion syndrome

SSSCA1 Gene

Sjogren syndrome/scleroderma autoantigen 1

This antigen is recognized by a subset of anti-centromere antibodies from patients with scleroderma and/or Sjogren's syndrome. Subcellular localization has not yet been established. [provided by RefSeq, Jul 2008]

SPG20 Gene

spastic paraplegia 20 (Troyer syndrome)

This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]

JBS Gene

Jacobsen syndrome

WS2B Gene

Waardenburg syndrome, type 2B

WS2C Gene

Waardenburg syndrome, type IIC

MRXSAB Gene

Abidi X-linked mental retardation syndrome

WHSC1 Gene

Wolf-Hirschhorn syndrome candidate 1

This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]

COHEN1 Gene

Cohen syndrome QTL 1

AOMS1 Gene

Abdominal obesity-metabolic syndrome QTL1

AOMS2 Gene

abdominal obesity-metabolic syndrome QTL2

DCR Gene

Down syndrome chromosome region

Down syndrome, the most frequent form of mental retardation caused by a microscopically demonstrable chromosomal aberration, is characterized by well-defined and distinctive phenotypic features and natural history. It is caused by triplicate state (trisomy) of all or a critical portion of chromosome 21.[supplied by OMIM, Apr 2005]

DUPXP11.22 Gene

Xp11.22 microduplication syndrome

DEL15Q11.2 Gene

Chromosome 15q11.2 deletion syndrome

HHT3 Gene

Osler-Rendu-Weber syndrome 3

DEL1Q43Q44 Gene

Chromosome 1q42-q44 deletion syndrome

OGS2 Gene

Opitz G syndrome, type II

This disorder, variously named the G, Opitz-G, or BBB syndrome, includes hypertelorism or telecanthus; laryngotracheoesophageal cleft; clefts of lip, palate, and uvula; swallowing difficulty and hoarse cry; genitourinary defects, especially hypospadias in males and splayed labia majora in females; mental retardation; and congenital heart defects.[supplied by OMIM, Jul 2002]

AMMECR1 Gene

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]

TUKLS Gene

Tukel syndrome

PIH2 Gene

pregnancy-induced hypertension syndrome-related protein

CXDUPQ26.3 Gene

Chromosome Xq26.3 duplication syndrome

LOC729770 Gene

wiskott-Aldrich syndrome protein homolog

HBHR Gene

alpha-thalassemia/mental retardation syndrome, type 1

NMLFS Gene

Nablus mask-like facial syndrome

BMIQ16 Gene

Chromosome 16p11.2 deletion syndrome, 220kb

DELYQ11 Gene

Sertoli cell-only syndrome, Y-linked

DEL19P13.13 Gene

Chromosome 19p13.13 deletion syndrome

DEL3PTERP25 Gene

3p- syndrome

TRIP4Q32.1Q32.2 Gene

Chromosome 4q32.1-q32.2 triplication syndrome

DEL3Q13.31 Gene

Chromosome 3q13.31 deletion syndrome

DEL15Q25 Gene

Chromosome 15q25 deletion syndrome

SSB Gene

Sjogren syndrome antigen B (autoantigen La)

The protein encoded by this gene is involved in diverse aspects of RNA metabolism, including binding and protecting poly(U) termini of nascent RNA polymerase III transcripts from exonuclease digestion, processing 5' and 3' ends of pre-tRNA precursors, acting as an RNA chaperone, and binding viral RNAs associated with hepatitis C virus. Autoantibodies reacting with this protein are found in the sera of patients with Sjogren syndrome and systemic lupus erythematosus. Alternative promoter usage results in two different transcript variants which encode the same protein. [provided by RefSeq, Jun 2014]

DELXP21 Gene

Chromosome Xp21 deletion syndrome

DEL17Q12 Gene

Chromosome 17q12 deletion syndrome

EDS8 Gene

Ehlers-Danlos syndrome, type VIII

LOC102724426 Gene

Sjoegren syndrome nuclear autoantigen 1 homolog

DSCR8 Gene

Down syndrome critical region 8

DSCR3 Gene

Down syndrome critical region 3

The region of chromosome 21 between genes CBR and ERG (CBR-ERG region), which spans 2.5 Mb on 21q22.2, has been defined by analysis of patients with partial trisomy 21. It contributes significantly to the pathogenesis of many characteristics of Down syndrome, including morphological features, hypotonia, and mental retardation. The DSCR3 (Down syndrome critical region gene 3) gene is found in this region and is predictated to contain eight exons. DSCR3 is expressed in most tissues examined. [provided by RefSeq, Jul 2008]

ALMS1 Gene

Alstrom syndrome protein 1

This gene encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations in this gene cause Alstrom syndrome. There is a pseudogene for this gene located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. [provided by RefSeq, Apr 2014]

TAM Gene

Myeloproliferative syndrome, transient (transient abnormal

WHCR Gene

Wolf-Hirschhorn syndrome chromosome region

Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]

DEL2Q23.1 Gene

Chromosome 2q23.1 deletion syndrome

WHSC1L1 Gene

Wolf-Hirschhorn syndrome candidate 1-like 1

This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. Two alternatively spliced variants have been described. [provided by RefSeq, May 2015]

ATRX Gene

alpha thalassemia/mental retardation syndrome X-linked

The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Aug 2013]

DUP16P11.2 Gene

Chromosome 16p11.2 duplication syndrome

MMDFS Gene

Multiple mitochondrial dysfunctions syndrome

DEL8Q21.11 Gene

Chromosome 8q21.11 deletion syndrome

CDL2 Gene

Cornelia de Lange syndrome 2

DEL3Q29 Gene

Chromosome 3q29 microdeletion syndrome

AMMEC Gene

Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis

DGCR9 Gene

DiGeorge syndrome critical region gene 9 (non-protein coding)

DGCR2 Gene

DiGeorge syndrome critical region gene 2

Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

DGCR5 Gene

DiGeorge syndrome critical region gene 5 (non-protein coding)

DGCR7 Gene

DiGeorge syndrome critical region gene 7

DGCR6 Gene

DiGeorge syndrome critical region gene 6

DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. The product of this gene shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the gamma-1 subunit of human laminin. This gene is a candidate for involvement in DiGeorge syndrome pathology and in schizophrenia. [provided by RefSeq, Nov 2008]

DEL9P Gene

Chromosome 9p deletion syndrome

LVSKS Gene

Levy-Shanske syndrome

ADFN Gene

albinism-deafness syndrome

GPDS1 Gene

glaucoma-related pigment dispersion syndrome 1

DEL2Q32Q33 Gene

Chromosome 2q32-q33 deletion syndrome

CECR5 Gene

cat eye syndrome chromosome region, candidate 5

CECR9 Gene

cat eye syndrome chromosome region, candidate 9 (non-protein coding)

LOC101929941 Gene

neural Wiskott-Aldrich syndrome protein-like

RIEG2 Gene

Rieger syndrome 2

DEL1Q41Q42 Gene

Chromosome 1q41-q42 deletion syndrome

SBDS Gene

Shwachman-Bodian-Diamond syndrome

This gene encodes a member of a highly conserved protein family that exists from archaea to vertebrates and plants. The encoded protein may function in RNA metabolism. Mutations within this gene are associated with Shwachman-Bodian-Diamond syndrome. An alternative transcript has been described, but its biological nature has not been determined. This gene has a closely linked pseudogene that is distally located. [provided by RefSeq, Jul 2008]

PSS Gene

Potocki-Shaffer syndrome

OCRL Gene

oculocerebrorenal syndrome of Lowe

This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008]

LOC100420893 Gene

Down syndrome critical region 3 pseudogene

PCOS1 Gene

polycystic ovary syndrome 1

WHSC1L2P Gene

Wolf-Hirschhorn syndrome candidate 1-like 2, pseudogene

DEL11P13 Gene

Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome

WBSCR27 Gene

Williams Beuren syndrome chromosome region 27

This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]

WBSCR28 Gene

Williams-Beuren syndrome chromosome region 28

DUP17Q23.1Q23.2 Gene

Chromosome 17q23.1-q23.2 duplication syndrome

FGS2 Gene

FG syndrome 2

FGS3 Gene

FG syndrome 3

HYLS1 Gene

hydrolethalus syndrome 1

This gene encodes a protein localized to the cytoplasm. Mutations in this gene are associated with hydrolethalus syndrome. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Oct 2008]

EVC2 Gene

Ellis van Creveld syndrome 2

This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

ACF Gene

Asymmetric crying facies (Cayler cardiofacial syndrome)

DEL6Q24Q25 Gene

Chromosome 6q25-q25 deletion syndrome

MYSA Gene

myasthenic (Lambert-Eaton) syndrome antigen A

INDX Gene

Immunoneurologic syndrome X-linked, of Wood, Black, and Norbury

SCLL Gene

Chromosome 8p11 myeloproliferative syndrome

ACLS Gene

acrocallosal syndrome

USHBP1 Gene

Usher syndrome 1C binding protein 1

LOC389465 Gene

Sjogren syndrome antigen B pseudogene

TEMPS Gene

Temple syndrome

GHS Gene

Goldenhar syndrome

KONDS Gene

Kondoh syndrome

NIPA2P3 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 3

NIPA2P2 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 2

NIPA2P1 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 1

NIPA2P5 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 5

NIPA2P4 Gene

non imprinted in Prader-Willi/Angelman syndrome 2 pseudogene 4

NHS Gene

Nance-Horan syndrome (congenital cataracts and dental anomalies)

This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014]

MROS Gene

Melkersson-Rosenthal syndrome

CECR1 Gene

cat eye syndrome chromosome region, candidate 1

This gene encodes a member of a subfamily of the adenosine deaminase protein family. The encoded protein is one of two adenosine deaminases found in humans, which regulate levels of the signaling molecule, adenosine. The encoded protein is secreted from monocytes undergoing differentiation and may regulate cell proliferation and differentiation. This gene may be responsible for some of the phenotypic features associated with cat eye syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

CECR2 Gene

cat eye syndrome chromosome region, candidate 2

This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

CECR3 Gene

cat eye syndrome chromosome region, candidate 3 (non-protein coding)

CECR6 Gene

cat eye syndrome chromosome region, candidate 6

DELXQ28 Gene

Chromosome Xq28 microdeletion syndrome

APMR3 Gene

Alopecia-mental retardation syndrome 3

APMR2 Gene

Alopecia with mental retardation syndrome 2

APMR1 Gene

Alopecia-mental retardation syndrome

COHEN2 Gene

Cohen syndrome QTL 2

DUP2Q31.1 Gene

Chromosome 2q31.1 duplication syndrome

MKKS Gene

McKusick-Kaufman syndrome

This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family. The encoded protein is a centrosome-shuttling protein and plays an important role in cytokinesis. This protein also interacts with other type II chaperonin members to form a complex known as the BBSome, which involves ciliary membrane biogenesis. This protein is encoded by a downstream open reading frame (dORF). Several upstream open reading frames (uORFs) have been identified, which repress the translation of the dORF, and two of which can encode small mitochondrial membrane proteins. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 6, also known as McKusick-Kaufman syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]

DEL22Q11.2 Gene

Chromosome 22q11.2 deletion syndrome, distal

USH2A Gene

Usher syndrome 2A (autosomal recessive, mild)

This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

DEL13Q14 Gene

Chromosome 13q14 deletion syndrome

DUP16P13.3 Gene

Chromosome 16p13.3 duplication syndrome

DEL6PTER Gene

Chromosome 6pter deletion syndrome

WRN Gene

Werner syndrome, RecQ helicase-like

This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging. [provided by RefSeq, Jul 2008]

DUPXQ28 Gene

Chromosome Xq28 duplication syndrome

DEL2P12P11.2 Gene

Chromosome 2p12-p11.2 deletion syndrome

ARCODS Gene

Ariculocondylar syndrome

MKS1 Gene

Meckel syndrome, type 1

The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

DGCR Gene

DiGeorge syndrome chromosome region

DiGeorge syndrome (DGS) comprises hypocalcemia arising from parathyroid hypoplasia, thymic hypoplasia, and outflow tract defects of the heart. Disturbance of cervical neural crest migration into the derivatives of the pharyngeal arches and pouches can account for the phenotype. Most cases result from a deletion of chromosome 22q11.2 (the DiGeorge syndrome chromosome region, or DGCR). Several genes are lost including the putative transcription factor TUPLE1 which is expressed in the appropriate distribution. This deletion may present with a variety of phenotypes: Shprintzen, or velocardiofacial, syndrome (VCFS; MIM 192430); conotruncal anomaly face (or Takao syndrome); and isolated outflow tract defects of the heart including tetralogy of Fallot, truncus arteriosus, and interrupted aortic arch. A collective acronym CATCH22 has been proposed for these differing presentations. A small number of cases of DGS have defects in other chromosomes, notably 10p13 (see MIM 601362). In the mouse, a transgenic Hox A3 (Hox 1.5) knockout produces a phenotype similar to DGS as do the teratogens retinoic acid and alcohol.[supplied by OMIM, Aug 2009]

LOC100421446 Gene

Wolf-Hirschhorn syndrome candidate 1-like 1 pseudogene

ANCR Gene

Angelman syndrome chromosome region

Angelman syndrome is characterized by mental retardation, movement or balance disorder, characteristic abnormal behaviors, and severe limitations in speech and language. Most cases are caused by absence of a maternal contribution to the imprinted region on chromosome 15q11-q13. Prader-Willi syndrome (PWS; MIM 176270) is a clinically distinct disorder resulting from paternal deletion of the same 15q11-q13 region. In addition, the chromosome 15q11-q13 duplication syndrome (MIM 608636) shows overlapping clinical features. Clayton-Smith and Pembrey (1992) [PubMed 1619637] provided a review of Angelman syndrome. Cassidy and Schwartz (1998) [PubMed 9556704] reviewed the molecular and clinical aspects of both Prader-Willi syndrome and Angelman syndrome. Horsthemke and Wagstaff (2008) [PubMed 18627066] provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome region.[supplied by OMIM, Oct 2008]

DEL2Q31 Gene

Chromosome 2q31.2 deletion syndrome

RJBS Gene

Rajab syndrome

DEL16P12.1P11.2 Gene

Chromosome 16p12.2-p11.2 deletion syndrome

MDNS Gene

Mammary-digital-nail syndrome

DEL2P16.1-P15 Gene

Chromosome 2p16.1-p15 deletion syndrome

WBSCR17 Gene

Williams-Beuren syndrome chromosome region 17

This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]

DEL6Q11Q14 Gene

Chromosome 6q11-q14 deletion syndrome

WAS Gene

Wiskott-Aldrich syndrome

The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5' UTR sequence, has been described, however, its full-length nature is not known. [provided by RefSeq, Jul 2008]

MEHMO Gene

mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome

MRXSA Gene

Armfield X-linked mental retardation syndrome

MRXSL Gene

Lubs X-linked mental retardation syndrome

RFMN Gene

Roifman syndrome

DUP22Q11.2 Gene

Chromosome 22q11.2 microduplication syndrome

DSCAM Gene

Down syndrome cell adhesion molecule

This gene is a member of the immunoglobulin superfamily of cell adhesion molecules (Ig-CAMs), and is involved in human central and peripheral nervous system development. This gene is a candidate for Down syndrome and congenital heart disease (DSCHD). A gene encoding a similar Ig-CAM protein is located on chromosome 11. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2012]

CATMANS Gene

Catel-Manzke syndrome

ICR4 Gene

ichthyosis congenita IV, ichthyosis-prematurity syndrome

LRSL Gene

Larsen-like syndrome

DUP7Q11.23 Gene

Chromosome 7q11.23 duplication syndrome

MRXSBWB Gene

Brooks-Wisniewski-Brown syndrome

MBS1 Gene

Moebius syndrome 1

MBS2 Gene

Moebius syndrome 2

MBS3 Gene

Moebius syndrome 3

THAS Gene

thoracoabdominal syndrome

DEL16P13.3 Gene

Chromosome 16p13.3 deletion syndrome

DSCR9 Gene

Down syndrome critical region 9 (non-protein coding)

DSCR4 Gene

Down syndrome critical region 4

The gene is found in a region of chromosome 21 that has been linked to the pathogenesis of Down syndrome. This gene is transcribed from a bi-directional promoter located in an endogenous retrovirus. [provided by RefSeq, Jan 2015]

DEL17Q23.1Q23.2 Gene

Chromosome 17q23.1-q23.2 deletion syndrome

AIC Gene

Aicardi syndrome

DEL1P32P31 Gene

Chromosome 1p32-p31 deletion syndrome

DUPXQ27.3Q28 Gene

Chromosome Xq27.3-q28 duplication syndrome

DEL14Q11Q22 Gene

Chromosome 14q11-q22 deletion syndrome

MCS Gene

Miles-Carpenter X-linked mental retardation syndrome

SPPM Gene

scapuloperoneal syndrome, myopathic type

DUP17P13.3 Gene

Chromosome 17p13.3 duplication syndrome

SMCR8 Gene

Smith-Magenis syndrome chromosome region, candidate 8

SMCR2 Gene

Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding)

SMCR5 Gene

Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding)

SMCR6 Gene

Smith-Magenis syndrome chromosome region, candidate 6 (non-protein coding)

CECR7 Gene

cat eye syndrome chromosome region, candidate 7 (non-protein coding)

CYLD Gene

cylindromatosis (turban tumor syndrome)

This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

DEL2P21 Gene

Hypotonia-cystinuria syndrome

WAGRO Gene

WAGRO syndrome

OFD1 Gene

oral-facial-digital syndrome 1

This gene is located on the X chromosome and encodes a centrosomal protein. A knockout mouse model has been used to study the effect of mutations in this gene. The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation. Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2. Many pseudogenes have been identified; a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome. Alternatively spliced transcripts have been described for this gene but the biological validity of these transcripts has not been determined. [provided by RefSeq, Jul 2008]

EDSS2 Gene

Ectodermal dysplasia-syndactyly syndrome 2

DELXP11.3 Gene

Chromosome Xp11.3 deletion syndrome

MRXSMP Gene

Martin-Probst deafness-mental retardation syndrome

MSD Gene

microcephaly with spastic diplegia (Paine syndrome)

PRS Gene

Prieto X-linked mental retardation syndrome

DUP17Q12 Gene

Chromosome 17q12 duplication syndrome

USH1K Gene

Usher syndrome 1K (autosomal recessive)

SPG38 Gene

spastic paraplegia 38 (autosomal dominant, Silver syndrome)

ALMS1P Gene

Alstrom syndrome 1 pseudogene

SBDSP1 Gene

Shwachman-Bodian-Diamond syndrome pseudogene 1

ACRPV Gene

Acropectorovertebral dysplasia (F syndrome)

ACRPS Gene

Acropectoral syndrome

PRBNS Gene

Pierre Robin syndrome

ZLS Gene

Zimmerman-Laband Syndrome

CCCSX Gene

Cerebral-cerebellar-coloboma syndrome, X-linked

WBSCR22 Gene

Williams Beuren syndrome chromosome region 22

This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]

WFS1 Gene

Wolfram syndrome 1 (wolframin)

This gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta-cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system. Mutations in this gene can also cause autosomal dominant deafness 6 (DFNA6), also known as DFNA14 or DFNA38. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]

DUP3Q29 Gene

chromosome 3q29 microduplication syndrome

DUPXP11.23P11.22 Gene

Chromosome Xp11.23-p11.22 duplication syndrome

ASPG1 Gene

Asperger syndrome, susceptibility to, 1

DEL18P Gene

Chromosome 18p deletion syndrome

DEL18Q Gene

Chromosome 18q deletion syndrome

FRTS1 Gene

Fanconi renotubular syndrome

PTLS Gene

Potocki-Lupski syndrome

CECR Gene

cat eye syndrome chromosome region

Cat eye syndrome (CES) is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. A small supernumerary chromosome (smaller than chromosome 21) is present, frequently has 2 centromeres, is bisatellited, and represents an inv dup(22)(q11).[supplied by OMIM, Aug 2009]

FGS5 Gene

FG syndrome 5

IPW Gene

imprinted in Prader-Willi syndrome (non-protein coding)

This gene is non-protein coding, is expressed exclusively from the paternal allele, and may play a role in the imprinting process. Mutations in this gene are associated with Prader-Willi syndrome. [provided by RefSeq, May 2010]

DER22T11-22 Gene

Emanuel syndrome

DGCR11 Gene

DiGeorge syndrome critical region gene 11 (non-protein coding)

DGCR10 Gene

DiGeorge syndrome critical region gene 10 (non-protein coding)

DGCR12 Gene

DiGeorge syndrome critical region gene 12 (non-protein coding)

DGCR14 Gene

DiGeorge syndrome critical region gene 14

This gene is located within the minimal DGS critical region (MDGCR) thought to contain the gene(s) responsible for a group of developmental disorders. These disorders include DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome, and some familial or sporadic conotruncal cardiac defects which have been associated with microdeletion of 22q11.2. The encoded protein may be a component of C complex spliceosomes, and the orthologous protein in the mouse localizes to the nucleus. [provided by RefSeq, Jul 2008]

DSCR10 Gene

Down syndrome critical region 10 (non-protein coding)

GTS Gene

Gilles de la Tourette syndrome

DEL15Q24 Gene

Chromosome 15q24 deletion syndrome

RCHTS Gene

Roifman-Chitayat syndrome

C16DELQ22 Gene

Chromosome 16q22 deletion syndrome

TRPS1 Gene

trichorhinophalangeal syndrome I

This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [provided by RefSeq, Jul 2008]

DEL15Q13.3 Gene

Chromosome 15q13.3 microdeletion syndrome

DWS Gene

dandy-walker syndrome

DUP1Q21 Gene

Chromosome 1q21.1 duplication syndrome

WBS2 Gene

Williams-Beuren syndrome type 2

WBSCR2 Gene

Williams-Beuren syndrome chromosome region 2

LFS3 Gene

Li-Fraumeni syndrome 3

ATD Gene

asphixiating thoracic dystrophy (chondroectodermal dysplasia-like syndrome)

USH1H Gene

Usher syndrome 1H (autosomal recessive)

USH1C Gene

Usher syndrome 1C (autosomal recessive, severe)

This gene encodes a scaffold protein that functions in the assembly of Usher protein complexes. The protein contains PDZ domains, a coiled-coil region with a bipartite nuclear localization signal and a PEST degradation sequence. Defects in this gene are the cause of Usher syndrome type 1C and non-syndromic sensorineural deafness autosomal recessive type 18. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

USH1G Gene

Usher syndrome 1G (autosomal recessive)

This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

USH1E Gene

Usher syndrome 1E (autosomal recessive, severe)

RSS Gene

Russell Silver syndrome

SCKL3 Gene

Seckel syndrome 3

WSN Gene

Waisman syndrome

RSCIS Gene

Radiation sensitivity/chromosome instability syndrome, autosomal dominant

DER22T8-22 Gene

Supernumerary der(22)t(8-22) syndrome

GUST Gene

Gustavson mental retardation syndrome (with microcephaly, optic

RLS3 Gene

Restless legs syndrome 3

RLS2 Gene

Restless legs syndrome 2

RLS1 Gene

Restless legs syndrome, susceptibility to

RLS7 Gene

Restless legs syndrome 7

RLS6 Gene

Restless legs syndrome, susceptibility to, 6

RLS5 Gene

Restless legs syndrome, susceptibility to, 5

RLS8 Gene

Restless legs syndrome, susceptibility to, 8

WASL Gene

Wiskott-Aldrich syndrome-like

This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013]

BBS9 Gene

Bardet-Biedl syndrome 9

This gene is downregulated by parathyroid hormone in osteoblastic cells, and therefore, is thought to be involved in parathyroid hormone action in bones. The exact function of this gene has not yet been determined. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

BBS1 Gene

Bardet-Biedl syndrome 1

Mutations in this gene have been observed in patients with the major form (type 1) of Bardet-Biedl syndrome. The encoded protein may play a role in eye, limb, cardiac and reproductive system development. [provided by RefSeq, Jul 2008]

BBS2 Gene

Bardet-Biedl syndrome 2

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]

BBS5 Gene

Bardet-Biedl syndrome 5

This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized. [provided by RefSeq, Jul 2008]

BBS4 Gene

Bardet-Biedl syndrome 4

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternative splice variants have been described but their predicted protein products have not been experimentally verified.[provided by RefSeq, Oct 2014]

BBS7 Gene

Bardet-Biedl syndrome 7

This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy; however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014]

NIPA2 Gene

non imprinted in Prader-Willi/Angelman syndrome 2

This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

NIPA1 Gene

non imprinted in Prader-Willi/Angelman syndrome 1

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]

LOC100500719 Gene

Hermansky-Pudlak syndrome 1 pseudogene

ATPLS Gene

antiphospholipid syndrome, familial

DEL1P36 Gene

Chromosome 1p36 deletion syndrome

DURS1 Gene

Duane retraction syndrome 1

VWSM Gene

Van der Woude syndrome modifier

DSCAML1 Gene

Down syndrome cell adhesion molecule like 1

LOC653588 Gene

Sjogren syndrome antigen B (autoantigen La) pseudogene

GTSCR1 Gene

Gilles de la Tourette syndrome chromosome region, candidate 1 (non-protein coding)

DEL17Q21.31 Gene

Microdeletion 17q21.31 syndrome

NS2 Gene

Noonan syndrome 2

RLS4 Gene

Restless legs syndrome 4

DEL7Q11.23 Gene

Chromosome 7q11.23 deletion syndrome, distal, 1.2Mb

AOS Gene

Adams-Oliver syndrome

BBS10 Gene

Bardet-Biedl syndrome 10

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10. [provided by RefSeq, Jan 2010]

BBS12 Gene

Bardet-Biedl syndrome 12

The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010]

CFSS Gene

craniofacioskeletal syndrome

SSNA1 Gene

Sjogren syndrome nuclear autoantigen 1

DUP17Q21.31 Gene

Chromosome 17q21.31 duplication syndrome

BOS2 Gene

Branchiootic syndrome 2

DEL19Q13.11 Gene

Chromosome 19q13.11 deletion syndrome

LOC100533757 Gene

Sjogren syndrome antigen B (autoantigen La) pseudogene

DEL10Q26 Gene

Chromosome 10q deletion syndrome

WBSCR16 Gene

Williams-Beuren syndrome chromosome region 16

This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

OTDD Gene

Otodental dysplasia chromosome deletion syndrome

DEL17Q11.2 Gene

chromosome 17q11.2 deletion syndrome

DUP8Q22.1 Gene

Leri pleonosteosis chromosome duplication syndrome

EEC2 Gene

ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 2

EEC1 Gene

ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1

DEL4Q21 Gene

Chromosome 4q21 deletion syndrome

DUP22Q13 Gene

Chromosome 22q13 duplication syndrome

DGCR6L Gene

DiGeorge syndrome critical region gene 6-like

This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome. [provided by RefSeq, Jul 2008]

WTRS Gene

Wittwer syndrome

DEL17P13.1 Gene

Chromosome 17p13.1 deletion syndrome

KTWS Gene

Klippel-Trenaunay-Weber syndrome

DEL11P15P14 Gene

Chromosome 11p15-p14 deletion syndrome

DEL1Q21 Gene

Chromosome 1q21.1 deletion syndrome

DEL8Q12Q21 Gene

Bor-Duane hydrocephalus contiguous gene syndrome

SLSN3 Gene

Senior-Loken syndrome 3

BZX Gene

Bazex syndrome

ARVCF Gene

armadillo repeat gene deleted in velocardiofacial syndrome

Armadillo Repeat gene deleted in Velo-Cardio-Facial syndrome (ARVCF) is a member of the catenin family. This family plays an important role in the formation of adherens junction complexes, which are thought to facilitate communication between the inside and outside environments of a cell. The ARVCF gene was isolated in the search for the genetic defect responsible for the autosomal dominant Velo-Cardio-Facial syndrome (VCFS), a relatively common human disorder with phenotypic features including cleft palate, conotruncal heart defects and facial dysmorphology. The ARVCF gene encodes a protein containing two motifs, a coiled coil domain in the N-terminus and a 10 armadillo repeat sequence in the midregion. Since these sequences can facilitate protein-protein interactions ARVCF is thought to function in a protein complex. In addition, ARVCF contains a predicted nuclear-targeting sequence suggesting that it may have a function as a nuclear protein. [provided by RefSeq, Jun 2010]

HPS5 Gene

Hermansky-Pudlak syndrome 5

This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of integrin, alpha-3. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 5. Multiple transcript variants encoding two distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

HPS4 Gene

Hermansky-Pudlak syndrome 4

This gene encodes a protein component of biogenesis of lysosome-related organelles complexes (BLOC). BLOC complexes are important for the formation of endosomal-lysosomal organelles such as melanosomes and platelet dense granules. Mutations in this gene result in subtype 4 of Hermansky-Pudlak syndrome, a form of albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

HPS6 Gene

Hermansky-Pudlak syndrome 6

This intronless gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 5 protein. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 6. [provided by RefSeq, Jul 2008]

HPS1 Gene

Hermansky-Pudlak syndrome 1

This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. The encoded protein is a component of three different protein complexes termed biogenesis of lysosome-related organelles complex (BLOC)-3, BLOC4, and BLOC5. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 1. Multiple transcript variants encoding distinct isoforms have been identified for this gene; the full-length sequences of some of these have not been determined yet. [provided by RefSeq, Jul 2008]

HPS3 Gene

Hermansky-Pudlak syndrome 3

This gene encodes a protein containing a potential clathrin-binding motif, consensus dileucine signals, and tyrosine-based sorting signals for targeting to vesicles of lysosomal lineage. The encoded protein may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 3. [provided by RefSeq, Apr 2015]

LCS1 Gene

lymphedema-cholestasis syndrome 1

bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; leukemia, myeloid, acute; melanoma; myelodysplastic syndromes; preleukemia; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, erythroblastic, acute; leukemia, megakaryoblastic, acute; leukemia, monocytic, acute; leukemia, myeloid; leukemia, myeloid, acute; leukemia, myelomonocytic, acute; leukemia, promyelocytic, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, erythroblastic, acute; leukemia, megakaryoblastic, acute; leukemia, monocytic, acute; leukemia, myeloid; leukemia, myeloid, acute; leukemia, myelomonocytic, acute; leukemia, promyelocytic, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial mediterranean fever; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid; leukemia, myeloid, acute; myelodysplastic syndromes; myeloid leukemia; polycythemia vera; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; leukemia, myeloid; myelodysplastic syndromes; myeloid leukemia; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute t cell leukemia; burkitt lymphoma; burkitt; acute lymphoblastic leukemia (type); leukemia, lymphocytic, acute, l1; leukemia-lymphoma, adult t-cell; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; leukemias, acute myeloblastic; precursor cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; leukemia, pre-b-cell; precursor b-cell lymphoblastic leukemia-lymphoma; precursor cell lymphoblastic leukemia-lymphoma; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blast crisis; leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelocytic, acute; leukemia, myeloid, acute; leukemias, acute myeloblastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelocytic, acute; leukemia, myeloid, acute; leukemias, acute myeloblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma; melanoma; neoplastic syndromes, hereditary; ovarian neoplasms; pancreatic neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemochromatosis; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemochromatosis; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; myelodysplastic syndromes; preleukemia; refractory anaemia -retired- in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndromes; parkinson disease; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndromes; parkinson disease; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sideroblastic; hemochromatosis; myelodysplastic syndromes; preleukemia; sideroblastic anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndromes; myeloproliferative disorders; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndromes; myeloproliferative disorders; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; myelodysplastic syndromes; myeloproliferative disorders; polycythemia vera; precursor cell lymphoblastic leukemia-lymphoma; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia; leukemia, myeloid; myeloid leukemia; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; leukemia; leukemia, myeloid; myeloid leukemia; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; esophageal neoplasms; lung neoplasms; prostatic neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung ; neoplasms; ovarian neoplasm; ovarian neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung ; neoplasms; ovarian neoplasm; ovarian neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hematologic diseases; hematologic neoplasms; leukemia, myeloid; myeloid leukemia; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hematologic diseases; hematologic neoplasms; leukemia, myeloid; myeloid leukemia; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, acute, l1; leukemia, lymphocytic, acute, l2; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; acute myelogenous leukemia; chronic myelogenous leukemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease acute lymphocytic leukemia; acute myelogenous leukemia; chronic myelogenous leukemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; chromosome breakage; colorectal neoplasms; genital neoplasms, female; mammary neoplasms; neoplasms; nijmegen breakage syndrome; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma; carcinoma, large cell; colorectal neoplasms; leukemia, lymphoid; lung neoplasms; neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma; carcinoma, large cell; colorectal neoplasms; leukemia, lymphoid; lung neoplasms; neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelomonocytic, chronic; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelomonocytic, chronic; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; myelodysplastic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; lung neoplasms; melanoma; neoplasm metastasis; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; breast neoplasms; laryngeal neoplasm; laryngeal neoplasms; mammary neoplasms; neoplasms; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; head and neck neoplasms; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; head and neck neoplasms; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; melanoma; ovarian neoplasm; ovarian neoplasms; uveal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; melanoma; ovarian neoplasm; ovarian neoplasms; uveal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; myeloid leukemia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; myeloid leukemia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; myeloid leukemia; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia; leukemia, myeloid; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; leukemia; leukemia, myeloid; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; leukemia, myelomonocytic, chronic; myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; precursor cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; leukemias, acute myeloblastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; leukemias, acute myeloblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; chronic myelogenous leukemia; leukemia Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease acute lymphocytic leukemia; chronic myelogenous leukemia; leukemia from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; acute myelogenous leukemia; B cell lymphoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease acute lymphocytic leukemia; acute myelogenous leukemia; B cell lymphoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

leukemia; leukemia, myelodysplastic (trlimds) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; leukemia, myelodysplastic (trlimds) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin disease; leukemia, myeloid, acute; neoplasms, second primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin disease; leukemia, myeloid, acute; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hematologic neoplasms; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hematologic neoplasms; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; neoplasms, second primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; dna damage; lung neoplasms; mammary neoplasms; neoplasm of lung ; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

facial neoplasms; horse diseases; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease facial neoplasms; horse diseases; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; hematologic neoplasms; precursor cell lymphoblastic leukemia-lymphoma; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; hematologic neoplasms; precursor cell lymphoblastic leukemia-lymphoma; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, pre-b-cell; neurotoxicity syndromes; precursor b-cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, pre-b-cell; neurotoxicity syndromes; precursor b-cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; esophageal neoplasms; head and neck neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; maxillary neoplasms; mouth neoplasms; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; lung neoplasms; neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; lung neoplasms; neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, prostatic; ovarian neoplasm; ovarian neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; fallopian tube neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; fallopian tube neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Myelodysplastic Syndromes Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myelodysplastic Syndromes from the curated CTD Gene-Disease Associations dataset.

chromosome breakage; dna damage; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome breakage; dna damage; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, refractory; anemia, sideroblastic; myelodysplastic syndromes; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndromes; purpura, thrombocytopenic, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoproliferative disorders; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoproliferative disorders; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Myelodysplastic Syndromes Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Myelodysplastic Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

dysplastic nevus syndrome; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dysplastic nevus syndrome; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatomycoses; postoperative complications; precancerous conditions; skin diseases, bacterial; skin diseases, viral; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; kidney diseases; leukemia; neurotoxicity syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neurotoxicity syndromes; pancreatic neoplasm; pancreatic neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neurotoxicity syndromes; pancreatic neoplasm; pancreatic neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplastic syndromes, hereditary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Leukemia, Myeloid, Acute Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Myeloid, Acute from the curated CTD Gene-Disease Associations dataset.

acute myeloid leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease acute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; xyy karyotype Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; xyy karyotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blast crisis; blast phase; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blast crisis; blast phase; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; leukemia, myeloid, acute; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; leukemia, myeloid, acute; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, acute myeloid; longevity; myelodysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, acute myeloid; longevity; myelodysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gram-negative bacterial infections; gram-positive bacterial infections; leukemia, myeloid, acute; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gram-negative bacterial infections; gram-positive bacterial infections; leukemia, myeloid, acute; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; monosomy; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; monosomy; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; neoplasm, residual; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; neoplasm, residual; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; neoplasm, residual Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; neoplasm, residual in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, acute myeloid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, acute myeloid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hematologic diseases; leukemia, myeloid, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hematologic diseases; leukemia, myeloid, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

GSK3A_KD_GDS4305_182_human_THP-1 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3A_KD_GDS4305_182_human_THP-1 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3B_KD_GDS4305_179_human_HL-60 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3B_KD_GDS4305_179_human_HL-60 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3A_KD_GDS4305_184_human_U937 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3A_KD_GDS4305_184_human_U937 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3B_KD_GDS4305_183_human_THP-1 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3B_KD_GDS4305_183_human_THP-1 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3B_KD_GDS4305_185_human_U937 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3B_KD_GDS4305_185_human_U937 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3A_KD_GDS4305_178_human_HL-60 acute myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3A_KD_GDS4305_178_human_HL-60 acute myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

acute myeloid leukemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease acute myeloid leukemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

acute myeloid leukemia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acute myeloid leukemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

acute myeloid leukemia Gene Set

From HPO Gene-Disease Associations

genes associated with the acute myeloid leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Leukemia, Myeloid, Acute Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Myeloid, Acute phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Acute myeloid leukemia 1 protein (AML1)/Runt Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acute myeloid leukemia 1 protein (AML1)/Runt protein domain from the InterPro Predicted Protein Domain Annotations dataset.

acute myeloid leukemia Gene Set

From KEGG Pathways

proteins participating in the acute myeloid leukemia pathway from the KEGG Pathways dataset.

leukemia, acute myeloid, with eosinophilia Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid, with eosinophilia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, acute myeloid, reduced survival in Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid, reduced survival in phenotype from the curated OMIM Gene-Disease Associations dataset.

{leukemia, acute myeloid, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {leukemia, acute myeloid, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{leukemia, acute myeloid} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {leukemia, acute myeloid} phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, acute myeloid, therapy-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid, therapy-related phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, acute myeloid, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

myeloid leukemia, acute, m4/m4eo subtype, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the myeloid leukemia, acute, m4/m4eo subtype, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, acute myeloid Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, acute myeloid phenotype from the curated OMIM Gene-Disease Associations dataset.

?leukemia, acute myeloid Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?leukemia, acute myeloid phenotype from the curated OMIM Gene-Disease Associations dataset.

acute myeloid leukemia cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue acute myeloid leukemia cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

acute myeloid leukemia cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue acute myeloid leukemia cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

acute myeloid leukemia cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue acute myeloid leukemia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; head and neck neoplasms; lip neoplasms; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Bloom syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bloom syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bloom Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bloom Syndrome from the curated CTD Gene-Disease Associations dataset.

bloom syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease bloom syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

bloom syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease bloom syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bloom syndrome; fanconi's anemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom syndrome; fanconi's anemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bloom's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Bloom Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Bloom Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

bloom syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the bloom syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Bloom's syndrome Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease Bloom's syndrome from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

crohn disease; crohn's disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; coronary artery disease; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma, amelanotic; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma, amelanotic; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasm invasiveness; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasm invasiveness; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cell transformation, neoplastic; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cell transformation, neoplastic; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

keratosis; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease keratosis; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperpigmentation; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperpigmentation; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasm metastasis; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasm metastasis; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic lymphocytic leukemia; leukemia, experimental; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic lymphocytic leukemia; leukemia, experimental; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

burkitt lymphoma; cell transformation, neoplastic; leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burkitt lymphoma; cell transformation, neoplastic; leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blast crisis; leukemia, megakaryoblastic, acute; leukemia, myelogenous, chronic, bcr-abl positive; primary myelofibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blast crisis; leukemia, megakaryoblastic, acute; leukemia, myelogenous, chronic, bcr-abl positive; primary myelofibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, acute, l1; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; bone marrow diseases; bone necrosis; edema; osteonecrosis; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute t cell leukemia; leukemia-lymphoma, adult t-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute t cell leukemia; leukemia-lymphoma, adult t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; hyperhomocysteinemia; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; hyperhomocysteinemia; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lymphocytic leukemia; precursor cell lymphoblastic leukemia-lymphoma; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; genital neoplasms, female; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

head and neck neoplasms; kidney neoplasms; lung neoplasms; neoplasms; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; kidney neoplasms; lung neoplasms; neoplasms; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; colorectal neoplasms; esophageal neoplasms; lung neoplasms; nasopharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; colorectal neoplasms; esophageal neoplasms; lung neoplasms; nasopharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; mouth neoplasms; squamous cell carcinoma; tongue neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; gingival neoplasms; mandibular neoplasms; mouth neoplasms; squamous cell carcinoma; tongue neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bladder neoplasm; esophageal neoplasms; leiomyoma; lung neoplasms; neoplasm of lung ; oesophageal neoplasm; urinary bladder neoplasms; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bladder neoplasm; esophageal neoplasms; leiomyoma; lung neoplasms; neoplasm of lung ; oesophageal neoplasm; urinary bladder neoplasms; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; neoplasms, prostatic; neoplasms, testis; prostatic neoplasms; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastrointestinal neoplasms; oesophageal neoplasm; pancreatic neoplasm; pancreatic neoplasms; squamous cell carcinoma; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, squamous cell; esophageal neoplasms; gastrointestinal neoplasms; oesophageal neoplasm; pancreatic neoplasm; pancreatic neoplasms; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; cervical neoplasm; esophageal neoplasms; mammary neoplasms; oesophageal neoplasm; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; cervical neoplasm; esophageal neoplasms; mammary neoplasms; oesophageal neoplasm; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; flushing; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; oesophageal neoplasm; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic neoplasms; lymphoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; lymphoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic neoplasms; neoplasms; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic neoplasms; neoplasms; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; melanoma; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; melanoma; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conjunctival neoplasms; melanoma; melanosis; nevus, pigmented; uveal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease conjunctival neoplasms; melanoma; melanosis; nevus, pigmented; uveal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; neoplasms, second primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; neoplasms, second primary; precursor b-cell lymphoblastic leukemia-lymphoma; precursor t-cell lymphoblastic leukemia-lymphoma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; neoplasms, second primary; precursor b-cell lymphoblastic leukemia-lymphoma; precursor t-cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neurotoxicity syndromes; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neurotoxicity syndromes; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-st-elevation acute coronary syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-st-elevation acute coronary syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary syndromes, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary syndromes, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bloom Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term bloom in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell; lymphoma; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; lupus erythematosus, systemic; mammary neoplasms; systemic lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; chronic b-cell leukemias; leukemia, lymphocytic, chronic, b-cell; lupus erythematosus, systemic; mammary neoplasms; systemic lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; precursor cell lymphoblastic leukemia-lymphoma; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; precursor cell lymphoblastic leukemia-lymphoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cachexia; gastrointestinal neoplasms; leukemia; lymphoma; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cachexia; gastrointestinal neoplasms; leukemia; lymphoma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, promyelocytic, acute; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, promyelocytic, acute; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelodysplastic syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the myelodysplastic syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

myelodysplastic syndrome, preleukemic Gene Set

From OMIM Gene-Disease Associations

genes associated with the myelodysplastic syndrome, preleukemic phenotype from the curated OMIM Gene-Disease Associations dataset.

{myelodysplastic syndrome, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {myelodysplastic syndrome, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myelodysplastic syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the myelodysplastic syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

neoplasms, basal cell; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, basal cell; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Preleukemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Preleukemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

skin melanoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease skin melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lung cancer; skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

skin cancer, non-melanoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease skin cancer, non-melanoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma skin cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma skin cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cutaneous melanoma which is largely independent of skin type and hair color Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Non-melanoma skin cancer Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Non-melanoma skin cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

skin melanoma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease skin melanoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

melanoma skin cancer Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease melanoma skin cancer from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; colorectal neoplasms; microsatellite instability; rectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; colorectal neoplasms; microsatellite instability; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; neoplasms; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; neoplasms; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; cell transformation, neoplastic; heart diseases; mammary neoplasms; neoplasms, experimental Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; cell transformation, neoplastic; heart diseases; mammary neoplasms; neoplasms, experimental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bladder neoplasm; breast neoplasms; mammary neoplasms; urinary bladder neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bladder neoplasm; breast neoplasms; mammary neoplasms; urinary bladder neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, squamous cell; lung neoplasms; mouth neoplasms; neoplasm of lung ; squamous cell carcinoma; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, squamous cell; lung neoplasms; mouth neoplasms; neoplasm of lung ; squamous cell carcinoma; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bladder neoplasm; neoplasms, prostatic; prostatic neoplasms; urinary bladder neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bladder neoplasm; neoplasms, prostatic; prostatic neoplasms; urinary bladder neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; adrenal neoplasm; carney complex; neoplasms, testis; sertoli cell tumor; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carney complex; neoplasms, testis; sertoli cell tumor; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; disease susceptibility; gastrointestinal neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; disease susceptibility; gastrointestinal neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; esophageal neoplasms; helicobacter infections; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; breast neoplasms, male; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; breast neoplasms, male; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; esophageal neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastrointestinal stromal tumors; liver neoplasms; lung neoplasms; neoplasm recurrence, local; neoplasm seeding; neoplasm, residual; splenic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastrointestinal stromal tumors; liver neoplasms; lung neoplasms; neoplasm recurrence, local; neoplasm seeding; neoplasm, residual; splenic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

laryngeal neoplasm; laryngeal neoplasms; neoplasms, second primary; neoplasms, squamous cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, second primary; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cervical neoplasm; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cervical neoplasm; endometrial neoplasms; ovarian neoplasm; ovarian neoplasms; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; esophageal neoplasms; oesophageal neoplasm; rectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; esophageal neoplasms; oesophageal neoplasm; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma; mammary neoplasms; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; carcinoma, squamous cell; esophageal neoplasms; laryngeal neoplasms; neoplasm invasiveness; oropharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; carcinoma, squamous cell; esophageal neoplasms; laryngeal neoplasms; neoplasm invasiveness; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, renal cell; endometrial neoplasms; kidney neoplasms; neoplasms; renal cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma, intraductal, noninfiltrating; carcinoma, lobular; mammary neoplasms; noninfiltrating intraductal carcinoma; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma, intraductal, noninfiltrating; carcinoma, lobular; mammary neoplasms; noninfiltrating intraductal carcinoma; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; neoplasms; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; neoplasms; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; fallopian tube neoplasms; ovarian neoplasm; ovarian neoplasms; peritoneal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; lung neoplasms; nervous system neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; lung neoplasms; nervous system neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; head and neck neoplasms; respiratory tract neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; hematologic neoplasms; hemochromatosis; hepatic veno-occlusive disease; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; neoplasms, germ cell and embryonal; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplasms, germ cell and embryonal; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; neoplasms, hormone-dependent; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplasms, hormone-dependent; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; lung neoplasms; mammary neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colonic polyps; colorectal neoplasms; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colonic polyps; colorectal neoplasms; mammary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; hyperhomocysteinemia; neoplasms; oesophageal neoplasm; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; hyperhomocysteinemia; neoplasms; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colonic neoplasms; colorectal neoplasms; rectal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colonic neoplasms; colorectal neoplasms; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; colorectal neoplasms; nasopharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; colorectal neoplasms; nasopharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; mouth neoplasms; papillomavirus infections; pharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; mouth neoplasms; papillomavirus infections; pharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bladder neoplasm; kidney neoplasms; ureteral neoplasms; urinary bladder neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bladder neoplasm; kidney neoplasms; ureteral neoplasms; urinary bladder neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; ovarian neoplasms; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; ovarian neoplasms; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, transitional cell; kidney neoplasms; neoplasm invasiveness; ureteral neoplasms; urinary bladder neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, transitional cell; kidney neoplasms; neoplasm invasiveness; ureteral neoplasms; urinary bladder neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; rectal neoplasms; sigmoid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; rectal neoplasms; sigmoid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; hypopharyngeal neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; hypopharyngeal neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, second primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; nevus; nevus, blue; uveal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; nevus; nevus, blue; uveal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma, follicular; carcinoma, papillary; melanoma; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma, follicular; carcinoma, papillary; melanoma; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; uveal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; uveal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye neoplasms; melanoma; tumour of eye Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye neoplasms; melanoma; tumour of eye in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; fragile x syndromes; movement disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; fragile x syndromes; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; fragile x syndromes; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; fragile x syndromes; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; fragile x syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia; fragile x syndrome; fragile x syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia; fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Leukemia, Myeloid Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Myeloid from the curated CTD Gene-Disease Associations dataset.

Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative from the curated CTD Gene-Disease Associations dataset.

Leukemia, Myeloid, Chronic-Phase Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Leukemia, Myeloid, Chronic-Phase in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

myeloid leukemia Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease myeloid leukemia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

chronic myeloid leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease chronic myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

myeloid leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

subacute myeloid leukemia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease subacute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

clonal evolution of chronic myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease clonal evolution of chronic myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, chronic-phase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, chronic-phase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome inversion; leukemia, myeloid; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

GSK3B_KD_GDS4305_181_human_MOLM-14 myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3B_KD_GDS4305_181_human_MOLM-14 myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

GSK3A_KD_GDS4305_180_human_MOLM-14 myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the GSK3A_KD_GDS4305_180_human_MOLM-14 myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

CREB_DEPLETION_GDS3487_41_human_K562 myeloid leukemia cell line Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the CREB_DEPLETION_GDS3487_41_human_K562 myeloid leukemia cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

Chronic myeloid leukemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Chronic myeloid leukemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

chronic myeloid leukemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease chronic myeloid leukemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

myeloid leukemia Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease myeloid leukemia in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

myeloid leukemia Gene Set

From HPO Gene-Disease Associations

genes associated with the myeloid leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Leukemia, Myeloid, Chronic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Myeloid, Chronic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Leukemia, Myeloid Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Myeloid phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Leukemia, Myeloid, Chronic-Phase Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukemia, Myeloid, Chronic-Phase phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Myeloid leukemia factor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myeloid leukemia factor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

chronic myeloid leukemia Gene Set

From KEGG Pathways

proteins participating in the chronic myeloid leukemia pathway from the KEGG Pathways dataset.

leukemia, myeloid/lymphoid or mixed-lineage Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, myeloid/lymphoid or mixed-lineage phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, chronic myeloid Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, chronic myeloid phenotype from the curated OMIM Gene-Disease Associations dataset.

chronic myeloid leukemia cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue chronic myeloid leukemia cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

myeloid leukemia cell Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue myeloid leukemia cell from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

myeloid leukemia cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue myeloid leukemia cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

m-1 myeloid leukemia cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue m-1 myeloid leukemia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

chronic myeloid leukemia cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue chronic myeloid leukemia cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

myeloid leukemia cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue myeloid leukemia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

chronic myeloid leukemia cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue chronic myeloid leukemia cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

AML - Acute myeloid leukemia_Mononuclear Leukocyte_GSE2191 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during AML - Acute myeloid leukemia_Mononuclear Leukocyte_GSE2191 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2924-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2924-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2862-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2862-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2813-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2813-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2943-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2943-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2885-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2885-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2987-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2987-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2986-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2986-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2884-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2884-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2925-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2925-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2849-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2849-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2824-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2824-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2828-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2828-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2851-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2851-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2814-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2814-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2916-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2916-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2955-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2955-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2971-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2971-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2981-03B-01T-0748-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2981-03B-01T-0748-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2988-03B-01T-0748-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2988-03B-01T-0748-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2929-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2929-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2826-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2826-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2888-03B-01T-0748-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2888-03B-01T-0748-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2977-03B-01T-0760-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2977-03B-01T-0760-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2915-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2915-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2881-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2881-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2880-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2880-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-3001-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-3001-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2867-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2867-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2821-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2821-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2980-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2980-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-3000-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-3000-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2975-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2975-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2820-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2820-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2896-03B-01T-0751-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2896-03B-01T-0751-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2920-03B-01T-0760-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2920-03B-01T-0760-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2992-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2992-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2901-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2901-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2842-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2842-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2853-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2853-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2861-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2861-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-3008-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-3008-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2939-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2939-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2919-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2919-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2890-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2890-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2803-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2803-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2832-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2832-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2917-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2917-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2807-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2807-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2985-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2985-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2982-03B-01T-0748-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2982-03B-01T-0748-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2933-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2933-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2843-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2843-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2904-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2904-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2899-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2899-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-3012-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-3012-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2886-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2886-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2859-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2859-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2941-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2941-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2875-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2875-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2972-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2972-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2963-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2963-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2818-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2818-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2931-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2931-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2983-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2983-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2836-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2836-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2909-03A-01T-0744-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2909-03A-01T-0744-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2816-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2816-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2956-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2956-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2952-03B-01T-0760-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2952-03B-01T-0760-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2978-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2978-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2946-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2946-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2870-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2870-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2856-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2856-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2903-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2903-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2825-03A-01T-0736-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2825-03A-01T-0736-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2834-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2834-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2928-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2928-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2822-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2822-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2871-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2871-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2935-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2935-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2879-03A-01T-0735-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2879-03A-01T-0735-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2839-03A-01T-0734-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2839-03A-01T-0734-13 relative to other tissue samples from the TCGA Signatures of Differentially Expressed Genes for Tumors dataset.

Acute Myeloid Leukemia_LAML_TCGA-AB-2921-03A-01T-0740-13 Gene Set

From TCGA Signatures of Differentially Expressed Genes for Tumors

genes with high or low expression in Acute Myeloid Leukemia_LAML_TCGA-AB-2921-03A-01T-0740-13 relative to other tissue samples from the TCGA Signatures of Di