Name

SCLL Gene

Chromosome 8p11 myeloproliferative syndrome

TAM Gene

Myeloproliferative syndrome, transient (transient abnormal

LOC613206 Gene

myeloproliferative disease associated tumor antigen 5

C19ORF12 Gene

chromosome 19 open reading frame 12

This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

C10ORF88 Gene

chromosome 10 open reading frame 88

LOC100288542 Gene

chromosome 14 open reading frame 119 pseudogene

C22ORF39 Gene

chromosome 22 open reading frame 39

C22ORF31 Gene

chromosome 22 open reading frame 31

C22ORF34 Gene

chromosome 22 open reading frame 34

C1ORF189 Gene

chromosome 1 open reading frame 189

C1ORF185 Gene

chromosome 1 open reading frame 185

C1ORF186 Gene

chromosome 1 open reading frame 186

CXORF58 Gene

chromosome X open reading frame 58

CXORF56 Gene

chromosome X open reading frame 56

While this gene is well-supported by transcript data, no functional information on its protein products is currently available. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]

CXORF57 Gene

chromosome X open reading frame 57

C12ORF4 Gene

chromosome 12 open reading frame 4

C14ORF119 Gene

chromosome 14 open reading frame 119

C18ORF15 Gene

chromosome 18 open reading frame 15

DUP5P13 Gene

Chromosome 5p13 duplication syndrome

C10ORF105 Gene

chromosome 10 open reading frame 105

C10ORF107 Gene

chromosome 10 open reading frame 107

BMIQ7 Gene

Obesity, susceptibility to, on chromosome 4

C1ORF234 Gene

chromosome 1 open reading frame 234

C2ORF81 Gene

chromosome 2 open reading frame 81

LOC100420788 Gene

chromosome 2 open reading frame 27A pseudogene

C14ORF79 Gene

chromosome 14 open reading frame 79

C20ORF96 Gene

chromosome 20 open reading frame 96

C17ORF47 Gene

chromosome 17 open reading frame 47

C17ORF49 Gene

chromosome 17 open reading frame 49

DEL15Q26QTER Gene

Chromosome 15q26-qter deletion syndrome

C11ORF49 Gene

chromosome 11 open reading frame 49

C11ORF40 Gene

chromosome 11 open reading frame 40

C11ORF42 Gene

chromosome 11 open reading frame 42

C11ORF45 Gene

chromosome 11 open reading frame 45

C19ORF18 Gene

chromosome 19 open reading frame 18

C7ORF43 Gene

chromosome 7 open reading frame 43

LOC100420668 Gene

chromosome 2 open reading frame 16 pseudogene

C9ORF118 Gene

chromosome 9 open reading frame 118

C9ORF117 Gene

chromosome 9 open reading frame 117

C9ORF116 Gene

chromosome 9 open reading frame 116

C9ORF114 Gene

chromosome 9 open reading frame 114

LOC724065 Gene

chromosome 19 open reading frame 53 pseudogene

C20ORF197 Gene

chromosome 20 open reading frame 197

C1ORF100 Gene

chromosome 1 open reading frame 100

C1ORF101 Gene

chromosome 1 open reading frame 101

C1ORF105 Gene

chromosome 1 open reading frame 105

C1ORF106 Gene

chromosome 1 open reading frame 106

C1ORF109 Gene

chromosome 1 open reading frame 109

LOC100526839 Gene

chromosome 18 open reading frame 32 pseudogene

LOC100526838 Gene

chromosome 18 open reading frame 32 pseudogene

C4ORF36 Gene

chromosome 4 open reading frame 36

C4ORF32 Gene

chromosome 4 open reading frame 32

C8ORF33 Gene

chromosome 8 open reading frame 33

C8ORF31 Gene

chromosome 8 open reading frame 31

C8ORF37 Gene

chromosome 8 open reading frame 37

This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]

C8ORF34 Gene

chromosome 8 open reading frame 34

C3ORF67 Gene

chromosome 3 open reading frame 67

C3ORF62 Gene

chromosome 3 open reading frame 62

XCE Gene

X chromosome controlling element

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]

DEL15Q11.2 Gene

Chromosome 15q11.2 deletion syndrome

C16ORF46 Gene

chromosome 16 open reading frame 46

LOC646058 Gene

chromosome 4 open reading frame 27 pseudogene

CXORF49B Gene

chromosome X open reading frame 49B

DEL1Q43Q44 Gene

Chromosome 1q42-q44 deletion syndrome

C10ORF82 Gene

chromosome 10 open reading frame 82

LOC100859919 Gene

chromosome 9 open reading frame 86 pseudogene 2

LOC100129478 Gene

chromosome 4 open reading frame 46 pseudogene

C1ORF27 Gene

chromosome 1 open reading frame 27

S7 Gene

surface antigen (chromosome 7) 2

C9ORF92 Gene

chromosome 9 open reading frame 92

C18ORF32 Gene

chromosome 18 open reading frame 32

C7ORF34 Gene

chromosome 7 open reading frame 34

C7ORF33 Gene

chromosome 7 open reading frame 33

C7ORF31 Gene

chromosome 7 open reading frame 31

CXDUPQ26.3 Gene

Chromosome Xq26.3 duplication syndrome

ADIPQTL2 Gene

Circulating adiponectin QTL on chromosome 5

C6ORF99 Gene

chromosome 6 open reading frame 99

BMIQ10 Gene

Obesity, susceptibility to, on chromosome 10q

BMIQ16 Gene

Chromosome 16p11.2 deletion syndrome, 220kb

DEL19P13.13 Gene

Chromosome 19p13.13 deletion syndrome

TRIP4Q32.1Q32.2 Gene

Chromosome 4q32.1-q32.2 triplication syndrome

C3CER1 Gene

chromosome 3 common eliminated region 1

DEL3Q13.31 Gene

Chromosome 3q13.31 deletion syndrome

C19ORF66 Gene

chromosome 19 open reading frame 66

C19ORF60 Gene

chromosome 19 open reading frame 60

C19ORF68 Gene

chromosome 19 open reading frame 68

C6ORF132 Gene

chromosome 6 open reading frame 132

C6ORF136 Gene

chromosome 6 open reading frame 136

C12ORF56 Gene

chromosome 12 open reading frame 56

DEL15Q25 Gene

Chromosome 15q25 deletion syndrome

C12ORF50 Gene

chromosome 12 open reading frame 50

NHCP1 Gene

non-histone chromosome protein 1

C21ORF33 Gene

chromosome 21 open reading frame 33

This gene encodes a potential mitochondrial protein that is a member of the DJ-1/PfpI gene family. This protein is overexpressed in fetal Down syndrome brain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

LOC101241902 Gene

chromosome 4 open reading frame 46 pseudogene

C2ORF49 Gene

chromosome 2 open reading frame 49

C2ORF48 Gene

chromosome 2 open reading frame 48

C2ORF44 Gene

chromosome 2 open reading frame 44

C2ORF47 Gene

chromosome 2 open reading frame 47

C2ORF40 Gene

chromosome 2 open reading frame 40

C2ORF42 Gene

chromosome 2 open reading frame 42

DELXP21 Gene

Chromosome Xp21 deletion syndrome

C20ORF141 Gene

chromosome 20 open reading frame 141

C20ORF144 Gene

chromosome 20 open reading frame 144

DEL17Q12 Gene

Chromosome 17q12 deletion syndrome

LOC100505642 Gene

chromosome 9 open reading frame 85 pseudogene

C8ORF89 Gene

chromosome 8 open reading frame 89

C8ORF88 Gene

chromosome 8 open reading frame 88

C8ORF82 Gene

chromosome 8 open reading frame 82

C8ORF87 Gene

chromosome 8 open reading frame 87

C8ORF86 Gene

chromosome 8 open reading frame 86

C14ORF169 Gene

chromosome 14 open reading frame 169

C14ORF166 Gene

chromosome 14 open reading frame 166

C6ORF10 Gene

chromosome 6 open reading frame 10

C6ORF15 Gene

chromosome 6 open reading frame 15

LOC105369237 Gene

sperm protein associated with the nucleus on the X chromosome B/F

C17ORF99 Gene

chromosome 17 open reading frame 99

C17ORF98 Gene

chromosome 17 open reading frame 98

C17ORF97 Gene

chromosome 17 open reading frame 97

C17ORF96 Gene

chromosome 17 open reading frame 96

C15ORF61 Gene

chromosome 15 open reading frame 61

C15ORF65 Gene

chromosome 15 open reading frame 65

C19ORF44 Gene

chromosome 19 open reading frame 44

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

C22ORF42 Gene

chromosome 22 open reading frame 42

C22ORF46 Gene

chromosome 22 open reading frame 46

C1ORF95 Gene

chromosome 1 open reading frame 95

C1ORF94 Gene

chromosome 1 open reading frame 94

HPCQTL19 Gene

Prostate cancer aggressiveness quantitative trait locus on chromosome 19

CXORF21 Gene

chromosome X open reading frame 21

CXORF23 Gene

chromosome X open reading frame 23

LOC727964 Gene

chromosome 2 open reading frame 69 pseudogene

LOC100420864 Gene

chromosome 11 open reading frame 58 pseudogene

C16ORF74 Gene

chromosome 16 open reading frame 74

C16ORF70 Gene

chromosome 16 open reading frame 70

C16ORF71 Gene

chromosome 16 open reading frame 71

C16ORF72 Gene

chromosome 16 open reading frame 72

C16ORF78 Gene

chromosome 16 open reading frame 78

C14ORF28 Gene

chromosome 14 open reading frame 28

C20ORF62 Gene

chromosome 20 open reading frame 62

DUP16P11.2 Gene

Chromosome 16p11.2 duplication syndrome

LOC389895 Gene

chromosome 16 open reading frame 72-like

C11ORF16 Gene

chromosome 11 open reading frame 16

C9ORF172 Gene

chromosome 9 open reading frame 172

C10ORF71 Gene

chromosome 10 open reading frame 71

C10ORF76 Gene

chromosome 10 open reading frame 76

C9ORF163 Gene

chromosome 9 open reading frame 163

C2ORF91 Gene

chromosome 2 open reading frame 91

DEL8Q21.11 Gene

Chromosome 8q21.11 deletion syndrome

C5ORF28 Gene

chromosome 5 open reading frame 28

C5ORF22 Gene

chromosome 5 open reading frame 22

C5ORF24 Gene

chromosome 5 open reading frame 24

C1ORF159 Gene

chromosome 1 open reading frame 159

C1ORF158 Gene

chromosome 1 open reading frame 158

C10ORF2 Gene

chromosome 10 open reading frame 2

This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009]

C2ORF66 Gene

chromosome 2 open reading frame 66

C3ORF18 Gene

chromosome 3 open reading frame 18

C3ORF14 Gene

chromosome 3 open reading frame 14

C3ORF17 Gene

chromosome 3 open reading frame 17

LOC647996 Gene

chromosome 9 open reading frame 172 pseudogene

C1ORF233 Gene

chromosome 1 open reading frame 233

DEL3Q29 Gene

Chromosome 3q29 microdeletion syndrome

RCBTB2P1 Gene

regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2 pseudogene 1

DEL9P Gene

Chromosome 9p deletion syndrome

LOC100289037 Gene

NHP2 non-histone chromosome protein 2-like 1 (S. cerevisiae) pseudogene

C9ORF62 Gene

chromosome 9 open reading frame 62

C9ORF66 Gene

chromosome 9 open reading frame 66

C9ORF64 Gene

chromosome 9 open reading frame 64

C9ORF69 Gene

chromosome 9 open reading frame 69

C12ORF60 Gene

chromosome 12 open reading frame 60

C12ORF66 Gene

chromosome 12 open reading frame 66

LOC100130170 Gene

chromosome 12 open reading frame 49 pseudogene

D6S2723E Gene

DNA segment on chromosome 6 (unique, pseudogene) 2723 expressed sequence

C11ORF98 Gene

chromosome 11 open reading frame 98

C11ORF97 Gene

chromosome 11 open reading frame 97

C11ORF96 Gene

chromosome 11 open reading frame 96

C11ORF95 Gene

chromosome 11 open reading frame 95

C11ORF94 Gene

chromosome 11 open reading frame 94

C11ORF91 Gene

chromosome 11 open reading frame 91

LOC100420831 Gene

chromosome 1 open reading frame 106 pseudogene

C6ORF163 Gene

chromosome 6 open reading frame 163

C6ORF165 Gene

chromosome 6 open reading frame 165

C2ORF16 Gene

chromosome 2 open reading frame 16

C2ORF15 Gene

chromosome 2 open reading frame 15

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)

C18ORF65 Gene

chromosome 18 open reading frame 65

C18ORF63 Gene

chromosome 18 open reading frame 63

C20ORF173 Gene

chromosome 20 open reading frame 173

LOC100420911 Gene

chromosome 14 open reading frame 166 pseudogene

C7ORF69 Gene

chromosome 7 open reading frame 69

C7ORF60 Gene

chromosome 7 open reading frame 60

C7ORF61 Gene

chromosome 7 open reading frame 61

C7ORF62 Gene

chromosome 7 open reading frame 62

C7ORF65 Gene

chromosome 7 open reading frame 65

C7ORF66 Gene

chromosome 7 open reading frame 66

LOC100287427 Gene

chromosome 18 open reading frame 21 pseudogene

LOC100287425 Gene

chromosome 7 open reading frame 73 pseudogene

DEL1Q41Q42 Gene

Chromosome 1q41-q42 deletion syndrome

C6ORF25 Gene

chromosome 6 open reading frame 25

This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SS18L2P2 Gene

synovial sarcoma translocation gene on chromosome 18-like 2 pseudogene 2

LOC100420892 Gene

chromosome 14 open reading frame 166 pseudogene

C14ORF93 Gene

chromosome 14 open reading frame 93

C15ORF32 Gene

chromosome 15 open reading frame 32

C19ORF35 Gene

chromosome 19 open reading frame 35

C11ORF44 Gene

chromosome 11 open reading frame 44

C21ORF62 Gene

chromosome 21 open reading frame 62

C21ORF2 Gene

chromosome 21 open reading frame 2

Four alternatively spliced transcript variants encoding four different isoforms have been found for this nuclear gene. All isoforms contain leucine-rich repeats. Three of these isoforms are mitochondrial proteins and one of them lacks the target peptide, so is not located in mitochondrion. This gene is down-regulated in Down syndrome (DS) brain, which may represent mitochondrial dysfunction in DS patients. [provided by RefSeq, Sep 2012]

LOC100129667 Gene

chromosome 5 open reading frame 13 pseudogene

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

C22ORF15 Gene

chromosome 22 open reading frame 15

DUP17Q23.1Q23.2 Gene

Chromosome 17q23.1-q23.2 duplication syndrome

C8ORF58 Gene

chromosome 8 open reading frame 58

C8ORF59 Gene

chromosome 8 open reading frame 59

C17ORF107 Gene

chromosome 17 open reading frame 107

C10ORF126 Gene

chromosome 10 open reading frame 126

C10ORF120 Gene

chromosome 10 open reading frame 120

C10ORF128 Gene

chromosome 10 open reading frame 128

C2ORF27A Gene

chromosome 2 open reading frame 27A

C2ORF27B Gene

chromosome 2 open reading frame 27B

C21ORF58 Gene

chromosome 21 open reading frame 58

DEL6Q24Q25 Gene

Chromosome 6q25-q25 deletion syndrome

LOC100132977 Gene

chromosome 2 open reading frame 27B pseudogene

C16ORF47 Gene

chromosome 16 open reading frame 47

C3ORF70 Gene

chromosome 3 open reading frame 70

C11ORF68 Gene

chromosome 11 open reading frame 68

C11ORF65 Gene

chromosome 11 open reading frame 65

C11ORF63 Gene

chromosome 11 open reading frame 63

C10ORF25 Gene

chromosome 10 open reading frame 25

C10ORF99 Gene

chromosome 10 open reading frame 99

LOC100127912 Gene

chromosome 2 open reading frame 27B pseudogene

C9ORF131 Gene

chromosome 9 open reading frame 131

C9ORF135 Gene

chromosome 9 open reading frame 135

C9ORF139 Gene

chromosome 9 open reading frame 139

C5ORF17 Gene

chromosome 5 open reading frame 17

C5ORF15 Gene

chromosome 5 open reading frame 15

C1ORF127 Gene

chromosome 1 open reading frame 127

C1ORF122 Gene

chromosome 1 open reading frame 122

C1ORF123 Gene

chromosome 1 open reading frame 123

C4ORF51 Gene

chromosome 4 open reading frame 51

C3ORF49 Gene

chromosome 3 open reading frame 49

C17ORF112 Gene

chromosome 17 open reading frame 112

C12ORF65 Gene

chromosome 12 open reading frame 65

This nuclear gene encodes a mitochondrial matrix protein that appears to contribute to peptide chain termination in the mitochondrial translation machinery. Two different 1 bp deletions (resulting in the same premature stop codon)result in decreased mitochondrial translation, decreased levels of oxidative phosphorylation complexes and encepthalomyopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

C9ORF50 Gene

chromosome 9 open reading frame 50

C9ORF57 Gene

chromosome 9 open reading frame 57

LOC100420839 Gene

chromosome 18 open reading frame 21 pseudogene

C20ORF196 Gene

chromosome 20 open reading frame 196

C20ORF195 Gene

chromosome 20 open reading frame 195

C19ORF84 Gene

chromosome 19 open reading frame 84

C19ORF80 Gene

chromosome 19 open reading frame 80

C19ORF81 Gene

chromosome 19 open reading frame 81

C14ORF37 Gene

chromosome 14 open reading frame 37

LOC100420683 Gene

chromosome X open reading frame 67 pseudogene

LOC100217367 Gene

chromosome 11 open reading frame 73 pseudogene

C1ORF43 Gene

chromosome 1 open reading frame 43

C20ORF57 Gene

chromosome 20 open reading frame 57

C18ORF54 Gene

chromosome 18 open reading frame 54

LOC100132570 Gene

chromosome 17 open reading frame 58 pseudogene

C7ORF13 Gene

chromosome 7 open reading frame 13

C4ORF33 Gene

chromosome 4 open reading frame 33

C12ORF10 Gene

chromosome 12 open reading frame 10

C15ORF41 Gene

chromosome 15 open reading frame 41

This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

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

LOC100420738 Gene

chromosome 9 open reading frame 78 pseudogene

LOC100131279 Gene

chromosome 2 open reading frame 69 pseudogene

RCC1 Gene

regulator of chromosome condensation 1

RCC2 Gene

regulator of chromosome condensation 2

ASOBS Gene

Asthma and obesity susceptibility, chromosome 16p11 inversion related

C17ORF104 Gene

chromosome 17 open reading frame 104

C17ORF105 Gene

chromosome 17 open reading frame 105

C17ORF102 Gene

chromosome 17 open reading frame 102

C17ORF100 Gene

chromosome 17 open reading frame 100

C21ORF59 Gene

chromosome 21 open reading frame 59

This gene a protein plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]

C10ORF90 Gene

chromosome 10 open reading frame 90

C10ORF91 Gene

chromosome 10 open reading frame 91

C10ORF95 Gene

chromosome 10 open reading frame 95

LOC284269 Gene

chromosome 9 open reading frame 86 pseudogene 1

C22ORF29 Gene

chromosome 22 open reading frame 29

C22ORF23 Gene

chromosome 22 open reading frame 23

C22ORF24 Gene

chromosome 22 open reading frame 24

DUP2Q31.1 Gene

Chromosome 2q31.1 duplication syndrome

CXORF49 Gene

chromosome X open reading frame 49

LOC100420966 Gene

chromosome 17 open reading frame 98 pseudogene

LOC100420967 Gene

chromosome 2 open reading frame 27B pseudogene

C6ORF1 Gene

chromosome 6 open reading frame 1

C6ORF7 Gene

chromosome 6 open reading frame 7

C14ORF105 Gene

chromosome 14 open reading frame 105

DEL22Q11.2 Gene

Chromosome 22q11.2 deletion syndrome, distal

LOC100502572 Gene

chromosome 5 open reading frame 60 pseudogene

DEL13Q14 Gene

Chromosome 13q14 deletion syndrome

C1ORF204 Gene

chromosome 1 open reading frame 204

DUP16P13.3 Gene

Chromosome 16p13.3 duplication syndrome

C20ORF85 Gene

chromosome 20 open reading frame 85

DEL6PTER Gene

Chromosome 6pter deletion syndrome

C6ORF201 Gene

chromosome 6 open reading frame 201

C17ORF70 Gene

chromosome 17 open reading frame 70

FAAP100 is a component of the Fanconi anemia (FA; MIM 277650) core complex and is required for core complex stability and FANCD2 (see MIM 227646) monoubiquitination (Ling et al., 2007 [PubMed 17396147]).[supplied by OMIM, Mar 2008]

C17ORF77 Gene

chromosome 17 open reading frame 77

C17ORF75 Gene

chromosome 17 open reading frame 75

C17ORF74 Gene

chromosome 17 open reading frame 74

C17ORF78 Gene

chromosome 17 open reading frame 78

SS18L2 Gene

synovial sarcoma translocation gene on chromosome 18-like 2

Synovial sarcomas occur most frequently in the extremities around large joints. More than 90% of cases have a recurrent and specific chromosomal translocation, t(X;18)(p11.2;q11.2), in which the 5-prime end of the SS18 gene (MIM 600192) is fused in-frame to the 3-prime end of the SSX1 (MIM 312820), SSX2 (MIM 300192), or SSX4 (MIM 300326) gene. The SS18L2 gene is homologous to SS18.[supplied by OMIM, Jul 2002]

SS18L1 Gene

synovial sarcoma translocation gene on chromosome 18-like 1

This gene encodes a calcium-responsive transactivator which is an essential subunit of a neuron-specific chromatin-remodeling complex. The structure of this gene is similar to that of the SS18 gene. Mutations in this gene are involved in amyotrophic lateral sclerosis (ALS). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

C10ORF10 Gene

chromosome 10 open reading frame 10

The expression of this gene is induced by fasting as well as by progesterone. The protein encoded by this gene contains a t-synaptosome-associated protein receptor (SNARE) coiled-coil homology domain and a peroxisomal targeting signal. Production of the encoded protein leads to phosphorylation and activation of the transcription factor ELK1. [provided by RefSeq, Jul 2008]

C10ORF11 Gene

chromosome 10 open reading frame 11

This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]

C10ORF12 Gene

chromosome 10 open reading frame 12

C8ORF49 Gene

chromosome 8 open reading frame 49

DUPXQ28 Gene

Chromosome Xq28 duplication syndrome

C9ORF106 Gene

chromosome 9 open reading frame 106

C5ORF49 Gene

chromosome 5 open reading frame 49

C5ORF45 Gene

chromosome 5 open reading frame 45

C5ORF46 Gene

chromosome 5 open reading frame 46

C5ORF47 Gene

chromosome 5 open reading frame 47

C5ORF42 Gene

chromosome 5 open reading frame 42

The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]

LOC105377772 Gene

chromosome alignment-maintaining phosphoprotein 1-like

DEL2P12P11.2 Gene

Chromosome 2p12-p11.2 deletion syndrome

C8ORF22 Gene

chromosome 8 open reading frame 22

C4ORF29 Gene

chromosome 4 open reading frame 29

C4ORF22 Gene

chromosome 4 open reading frame 22

C4ORF27 Gene

chromosome 4 open reading frame 27

C4ORF26 Gene

chromosome 4 open reading frame 26

Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene is thought to encode an extracellular matrix acidic phosphoprotein that has a function in enamel mineralization during amelogenesis. Mutations in this gene are associated with recessive hypomineralized amelogenesis imperfecta. [provided by RefSeq, Oct 2012]

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]

C14ORF180 Gene

chromosome 14 open reading frame 180

LOC100887076 Gene

chromosome 9 open reading frame 172 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

C16ORF45 Gene

chromosome 16 open reading frame 45

LOC646408 Gene

chromosome 9 open reading frame 16 pseudogene

C16ORF58 Gene

chromosome 16 open reading frame 58

This gene encodes a putative transmembrane protein containing a conserved DUF647 domain that may be involved in protein-protein interaction. The encoded protein is related to a plant protein that participates in ultraviolet B light-sensing during root morphogenesis. [provided by RefSeq, Feb 2013]

C16ORF59 Gene

chromosome 16 open reading frame 59

C16ORF52 Gene

chromosome 16 open reading frame 52

C16ORF54 Gene

chromosome 16 open reading frame 54

DEL16P12.1P11.2 Gene

Chromosome 16p12.2-p11.2 deletion syndrome

C2ORF82 Gene

chromosome 2 open reading frame 82

CHTF8 Gene

CTF8, chromosome transmission fidelity factor 8 homolog (S. cerevisiae)

This gene encodes a short protein that forms part of the Ctf18 replication factor C (RFC) complex that occurs in both yeast and mammals. The heteroheptameric RFC complex plays a role in sister chromatid cohesion and may load the replication clamp PCNA (proliferating cell nuclear antigen) onto DNA during DNA replication and repair. This gene is ubiquitously expressed and has been shown to have reduced expression in renal and prostate tumors. Alternatively spliced transcript variants have been described. This gene has a pseudogene on chromosome X. [provided by RefSeq, Jan 2010]

C11ORF31 Gene

chromosome 11 open reading frame 31

This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. The exact function of this gene is not known, however, selenoproteins are thought to be responsible for most biomedical effects of dietary selenium. [provided by RefSeq, Jul 2008]

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]

C5ORF34 Gene

chromosome 5 open reading frame 34

C1ORF147 Gene

chromosome 1 open reading frame 147

LOC100506911 Gene

chromosome 6 open reading frame 35 pseudogene

LOC642614 Gene

chromosome 2 open reading frame 69 pseudogene

DEL6Q11Q14 Gene

Chromosome 6q11-q14 deletion syndrome

C6ORF183 Gene

chromosome 6 open reading frame 183

C11ORF1 Gene

chromosome 11 open reading frame 1

ALS2CR11 Gene

amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 11

ALS2CR12 Gene

amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 12

C1ORF174 Gene

chromosome 1 open reading frame 174

C1ORF177 Gene

chromosome 1 open reading frame 177

C1ORF35 Gene

chromosome 1 open reading frame 35

DUP22Q11.2 Gene

Chromosome 22q11.2 microduplication syndrome

LOC100289470 Gene

chromosome 5 open reading frame 60 pseudogene

LOC101241901 Gene

chromosome 4 open reading frame 46 pseudogene

C9ORF89 Gene

chromosome 9 open reading frame 89

C9ORF84 Gene

chromosome 9 open reading frame 84

C9ORF85 Gene

chromosome 9 open reading frame 85

C1ORF68 Gene

chromosome 1 open reading frame 68

C6ORF89 Gene

chromosome 6 open reading frame 89

C12ORF49 Gene

chromosome 12 open reading frame 49

C12ORF40 Gene

chromosome 12 open reading frame 40

C12ORF43 Gene

chromosome 12 open reading frame 43

C12ORF42 Gene

chromosome 12 open reading frame 42

C12ORF45 Gene

chromosome 12 open reading frame 45

LOC100132615 Gene

chromosome 12 open reading frame 49 pseudogene

C19ORF53 Gene

chromosome 19 open reading frame 53

C19ORF52 Gene

chromosome 19 open reading frame 52

C19ORF57 Gene

chromosome 19 open reading frame 57

C19ORF54 Gene

chromosome 19 open reading frame 54

C6ORF106 Gene

chromosome 6 open reading frame 106

DUP7Q11.23 Gene

Chromosome 7q11.23 duplication syndrome

C20ORF194 Gene

chromosome 20 open reading frame 194

This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]

C19ORF71 Gene

chromosome 19 open reading frame 71

C2ORF70 Gene

chromosome 2 open reading frame 70

C2ORF71 Gene

chromosome 2 open reading frame 71

The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]

C2ORF73 Gene

chromosome 2 open reading frame 73

C2ORF74 Gene

chromosome 2 open reading frame 74

C2ORF76 Gene

chromosome 2 open reading frame 76

C2ORF78 Gene

chromosome 2 open reading frame 78

C6ORF120 Gene

chromosome 6 open reading frame 120

C21ORF140 Gene

chromosome 21 open reading frame 140

C7ORF49 Gene

chromosome 7 open reading frame 49

C14ORF159 Gene

chromosome 14 open reading frame 159

SS18L2P1 Gene

synovial sarcoma translocation gene on chromosome 18-like 2 pseudogene 1

DEL16P13.3 Gene

Chromosome 16p13.3 deletion syndrome

LOC100420743 Gene

chromosome 6 open reading frame 58 pseudogene

C17ORF89 Gene

chromosome 17 open reading frame 89

C17ORF82 Gene

chromosome 17 open reading frame 82

C17ORF80 Gene

chromosome 17 open reading frame 80

C17ORF85 Gene

chromosome 17 open reading frame 85

C15ORF59 Gene

chromosome 15 open reading frame 59

C15ORF57 Gene

chromosome 15 open reading frame 57

C15ORF56 Gene

chromosome 15 open reading frame 56

C15ORF54 Gene

chromosome 15 open reading frame 54

C15ORF53 Gene

chromosome 15 open reading frame 53

C15ORF52 Gene

chromosome 15 open reading frame 52

LOC647503 Gene

NHP2 non-histone chromosome protein 2-like 1 (S. cerevisiae) pseudogene

TSG11 Gene

Tumor suppressor gene on chromosome 11

DEL17Q23.1Q23.2 Gene

Chromosome 17q23.1-q23.2 deletion syndrome

DEL1P32P31 Gene

Chromosome 1p32-p31 deletion syndrome

C8ORF76 Gene

chromosome 8 open reading frame 76

C8ORF74 Gene

chromosome 8 open reading frame 74

C16ORF86 Gene

chromosome 16 open reading frame 86

C10ORF142 Gene

chromosome 10 open reading frame 142

DUPXQ27.3Q28 Gene

Chromosome Xq27.3-q28 duplication syndrome

DEL14Q11Q22 Gene

Chromosome 14q11-q22 deletion syndrome

C8ORF4 Gene

chromosome 8 open reading frame 4

This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/beta-catenin signaling pathway. This protein interacts with a repressor of beta-catenin mediated transcription at nuclear speckles. It is thought to competitively block interactions of the repressor with beta-catenin, resulting in up-regulation of beta-catenin target genes. The encoded protein may also play a role in the NF-kappaB and ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, breast cancer and hematological malignancies. [provided by RefSeq, Nov 2011]

LOC100420879 Gene

chromosome 2 open reading frame 27B pseudogene

ASPSCR1 Gene

alveolar soft part sarcoma chromosome region, candidate 1

The protein encoded by this gene contains a UBX domain and interacts with glucose transporter type 4 (GLUT4). This protein is a tether, which sequesters the GLUT4 in intracellular vesicles in muscle and fat cells in the absence of insulin, and redistributes the GLUT4 to the plasma membrane within minutes of insulin stimulation. Translocation t(X;17)(p11;q25) of this gene with transcription factor TFE3 gene results in a ASPSCR1-TFE3 fusion protein in alveolar soft part sarcoma and in renal cell carcinomas. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Oct 2011]

C14ORF39 Gene

chromosome 14 open reading frame 39

LOC100129574 Gene

chromosome 12 open reading frame 29 pseudogene

DUP17P13.3 Gene

Chromosome 17p13.3 duplication syndrome

LOC642669 Gene

chromosome 2 open reading frame 27A pseudogene

C1ORF21 Gene

chromosome 1 open reading frame 21

C12ORF73 Gene

chromosome 12 open reading frame 73

C12ORF76 Gene

chromosome 12 open reading frame 76

C6ORF203 Gene

chromosome 6 open reading frame 203

LOC644525 Gene

chromosome 2 open reading frame 27A pseudogene

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)

C9ORF156 Gene

chromosome 9 open reading frame 156

LOC100301521 Gene

chromosome 15 open reading frame 40 pseudogene

C9ORF153 Gene

chromosome 9 open reading frame 153

C9ORF152 Gene

chromosome 9 open reading frame 152

LOC100652967 Gene

chromosome 14 open reading frame 2 pseudogene

C2ORF80 Gene

chromosome 2 open reading frame 80

C2ORF88 Gene

chromosome 2 open reading frame 88

C5ORF38 Gene

chromosome 5 open reading frame 38

C5ORF30 Gene

chromosome 5 open reading frame 30

C1ORF145 Gene

chromosome 1 open reading frame 145

C1ORF146 Gene

chromosome 1 open reading frame 146

C1ORF141 Gene

chromosome 1 open reading frame 141

C1ORF143 Gene

chromosome 1 open reading frame 143

C3ORF20 Gene

chromosome 3 open reading frame 20

C3ORF22 Gene

chromosome 3 open reading frame 22

CXORF51B Gene

chromosome X open reading frame 51B

CXORF51A Gene

chromosome X open reading frame 51A

RCC2P1 Gene

regulator of chromosome condensation 2 pseudogene 1

RCC2P2 Gene

regulator of chromosome condensation 2 pseudogene 2

RCC2P3 Gene

regulator of chromosome condensation 2 pseudogene 3

RCC2P4 Gene

regulator of chromosome condensation 2 pseudogene 4

RCC2P5 Gene

regulator of chromosome condensation 2 pseudogene 5

RCC2P6 Gene

regulator of chromosome condensation 2 pseudogene 6

RCC2P7 Gene

regulator of chromosome condensation 2 pseudogene 7

RCC2P8 Gene

regulator of chromosome condensation 2 pseudogene 8

C9ORF72 Gene

chromosome 9 open reading frame 72

The protein encoded by this gene plays an important role in the regulation of endosomal trafficking, and has been shown to interact with Rab proteins that are involved in autophagy and endocytic transport. Expansion of a hexanucleotide repeat in non-coding sequence between alternate 5' exons in transcripts from this gene is associated with 9p-linked ALS (amyotrophic lateral sclerosis) and FTD (frontotemporal dementia) (PMID: 21944778, 21944779). Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA, and the accumulation of insoluble dipeptide repeat protein aggregates that could be pathogenic in FTD-ALS patients (PMID: 23393093). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]

C16ORF89 Gene

chromosome 16 open reading frame 89

This gene is expressed predominantly in the thyroid. Based on expression patterns similar to thyroid transcription factors and proteins, this gene may function in the development and function of the thyroid. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

C16ORF82 Gene

chromosome 16 open reading frame 82

C16ORF87 Gene

chromosome 16 open reading frame 87

C11ORF88 Gene

chromosome 11 open reading frame 88

C11ORF87 Gene

chromosome 11 open reading frame 87

CSE1L Gene

CSE1 chromosome segregation 1-like (yeast)

Proteins that carry a nuclear localization signal (NLS) are transported into the nucleus by the importin-alpha/beta heterodimer. Importin-alpha binds the NLS, while importin-beta mediates translocation through the nuclear pore complex. After translocation, RanGTP binds importin-beta and displaces importin-alpha. Importin-alpha must then be returned to the cytoplasm, leaving the NLS protein behind. The protein encoded by this gene binds strongly to NLS-free importin-alpha, and this binding is released in the cytoplasm by the combined action of RANBP1 and RANGAP1. In addition, the encoded protein may play a role both in apoptosis and in cell proliferation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]

CECR7 Gene

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

C3ORF79 Gene

chromosome 3 open reading frame 79

C12ORF71 Gene

chromosome 12 open reading frame 71

C12ORF74 Gene

chromosome 12 open reading frame 74

C12ORF75 Gene

chromosome 12 open reading frame 75

C12ORF77 Gene

chromosome 12 open reading frame 77

C12ORF79 Gene

chromosome 12 open reading frame 79

C15ORF39 Gene

chromosome 15 open reading frame 39

C11ORF84 Gene

chromosome 11 open reading frame 84

C11ORF85 Gene

chromosome 11 open reading frame 85

C11ORF86 Gene

chromosome 11 open reading frame 86

C11ORF80 Gene

chromosome 11 open reading frame 80

C11ORF72 Gene

chromosome 11 open reading frame 72

C19ORF33 Gene

chromosome 19 open reading frame 33

C19ORF38 Gene

chromosome 19 open reading frame 38

C19ORF67 Gene

chromosome 19 open reading frame 67

C1ORF61 Gene

chromosome 1 open reading frame 61

C1ORF64 Gene

chromosome 1 open reading frame 64

DELXP11.3 Gene

Chromosome Xp11.3 deletion syndrome

C7ORF73 Gene

chromosome 7 open reading frame 73

C7ORF72 Gene

chromosome 7 open reading frame 72

C7ORF71 Gene

chromosome 7 open reading frame 71

C10ORF55 Gene

chromosome 10 open reading frame 55

IGHDOR15@ Gene

immunoglobulin heavy diversity orphans on chromosome 15

CHTF18 Gene

CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae)

CHTF18, CHTF8 (MIM 613202), and DCC1 (DSCC1; MIM 613203) are components of an alternative replication factor C (RFC) (see MIM 600404) complex that loads PCNA (MIM 176740) onto DNA during S phase of the cell cycle (Merkle et al., 2003 [PubMed 12766176]; Bermudez et al., 2003 [PubMed 12930902]).[supplied by OMIM, Dec 2009]

ADIPQTL3 Gene

Circulating adiponectin QTL on chromosome 14

C6ORF52 Gene

chromosome 6 open reading frame 52

C6ORF58 Gene

chromosome 6 open reading frame 58

DUP17Q12 Gene

Chromosome 17q12 duplication syndrome

LOC391636 Gene

chromosome 9 open reading frame 78 pseudogene

C15ORF26 Gene

chromosome 15 open reading frame 26

C15ORF27 Gene

chromosome 15 open reading frame 27

C19ORF26 Gene

chromosome 19 open reading frame 26

C19ORF24 Gene

chromosome 19 open reading frame 24

C19ORF25 Gene

chromosome 19 open reading frame 25

LOC647086 Gene

chromosome 20 open reading frame 27 pseudogene

LOC100129996 Gene

chromosome 6 open reading frame 203 pseudogene

SS18 Gene

synovial sarcoma translocation, chromosome 18

C1ORF198 Gene

chromosome 1 open reading frame 198

C1ORF196 Gene

chromosome 1 open reading frame 196

C1ORF195 Gene

chromosome 1 open reading frame 195

C1ORF194 Gene

chromosome 1 open reading frame 194

CXORF65 Gene

chromosome X open reading frame 65

CXORF67 Gene

chromosome X open reading frame 67

CXORF66 Gene

chromosome X open reading frame 66

The protein encoded by this gene is predicted to be a type I membrane protein, however, its exact function is not known. [provided by RefSeq, Sep 2009]

C8ORF48 Gene

chromosome 8 open reading frame 48

C8ORF46 Gene

chromosome 8 open reading frame 46

C8ORF44 Gene

chromosome 8 open reading frame 44

C10ORF113 Gene

chromosome 10 open reading frame 113

C10ORF111 Gene

chromosome 10 open reading frame 111

C1ORF226 Gene

chromosome 1 open reading frame 226

C1ORF228 Gene

chromosome 1 open reading frame 228

LOC100505524 Gene

chromosome 5 open reading frame 63 pseudogene

LOC729141 Gene

chromosome 18 open reading frame 25 pseudogene

C9ORF3 Gene

chromosome 9 open reading frame 3

This gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc-dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]

C9ORF9 Gene

chromosome 9 open reading frame 9

C17ORF59 Gene

chromosome 17 open reading frame 59

C17ORF58 Gene

chromosome 17 open reading frame 58

C17ORF51 Gene

chromosome 17 open reading frame 51

C17ORF50 Gene

chromosome 17 open reading frame 50

C17ORF53 Gene

chromosome 17 open reading frame 53

C11ORF58 Gene

chromosome 11 open reading frame 58

C11ORF53 Gene

chromosome 11 open reading frame 53

C11ORF52 Gene

chromosome 11 open reading frame 52

C11ORF57 Gene

chromosome 11 open reading frame 57

C11ORF54 Gene

chromosome 11 open reading frame 54

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]

C10ORF35 Gene

chromosome 10 open reading frame 35

C10ORF32 Gene

chromosome 10 open reading frame 32

C1ORF132 Gene

chromosome 1 open reading frame 132

DUP3Q29 Gene

chromosome 3q29 microduplication syndrome

C9ORF129 Gene

chromosome 9 open reading frame 129

DUPXP11.23P11.22 Gene

Chromosome Xp11.23-p11.22 duplication syndrome

C20ORF187 Gene

chromosome 20 open reading frame 187

C20ORF181 Gene

chromosome 20 open reading frame 181

C5ORF66 Gene

chromosome 5 open reading frame 66

C5ORF67 Gene

chromosome 5 open reading frame 67

C5ORF64 Gene

chromosome 5 open reading frame 64

C5ORF63 Gene

chromosome 5 open reading frame 63

C5ORF60 Gene

chromosome 5 open reading frame 60

LOC728024 Gene

chromosome X open reading frame 56 pseudogene

C1ORF112 Gene

chromosome 1 open reading frame 112

C1ORF111 Gene

chromosome 1 open reading frame 111

C1ORF110 Gene

chromosome 1 open reading frame 110

C1ORF116 Gene

chromosome 1 open reading frame 116

C1ORF115 Gene

chromosome 1 open reading frame 115

C4ORF47 Gene

chromosome 4 open reading frame 47

C4ORF46 Gene

chromosome 4 open reading frame 46

This gene encodes a small, conserved protein of unknown function that is expressed in a variety of tissues. There are pseudogenes for this gene on chromosomes 6, 8, 16, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]

C4ORF45 Gene

chromosome 4 open reading frame 45

C4ORF48 Gene

chromosome 4 open reading frame 48

C3ORF58 Gene

chromosome 3 open reading frame 58

C3ORF52 Gene

chromosome 3 open reading frame 52

C3ORF56 Gene

chromosome 3 open reading frame 56

RCBTB2 Gene

regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 2

This gene encodes a protein containing two C-terminal BTB/POZ domains that is related to regulator of chromosome condensation (RCC). The encoded protein may act as a guanine nucleotide exchange factor. This gene is observed to be lost or underexpressed in prostate cancers. There is a pseudogene of this gene on chromosome 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]

RCBTB1 Gene

regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1

This gene encodes a protein with an N-terminal RCC1 domain and a C-terminal BTB (broad complex, tramtrack and bric-a-brac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCBTB1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in B-cell chronic lymphocytic leukemia and other lymphoid malignancies. [provided by RefSeq, Jul 2008]

DUP18PDEL18Q Gene

Chromosome 18 pericentric inversion

LOC441320 Gene

chromosome 11 open reading frame2 pseudogene

DEL18P Gene

Chromosome 18p deletion syndrome

DEL18Q Gene

Chromosome 18q deletion syndrome

C9ORF24 Gene

chromosome 9 open reading frame 24

This gene encodes a nuclear- or perinuclear-localized protein with no predicted domains or similarity to other known proteins. Expression of this gene is induced during the differentiation of bronchial epithelial cells, and the encoded protein may play a role in ciliogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

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]

LOC100420928 Gene

chromosome 15 open reading frame 43 pseudogene

C14ORF2 Gene

chromosome 14 open reading frame 2

C11ORF39 Gene

chromosome 11 open reading frame 39

C14ORF1 Gene

chromosome 14 open reading frame 1

C11ORF30 Gene

chromosome 11 open reading frame 30

SCZD11 Gene

Schizophrenia susceptibility locus, chromosome 10q-related

C20ORF27 Gene

chromosome 20 open reading frame 27

C20ORF24 Gene

chromosome 20 open reading frame 24

CHAMP1 Gene

chromosome alignment maintaining phosphoprotein 1

C14ORF132 Gene

chromosome 14 open reading frame 132

LOC100526841 Gene

chromosome 18 open reading frame 32 pseudogene

LOC441750 Gene

chromosome 12 open reading frame 49 pseudogene

CPXCR1 Gene

CPX chromosome region, candidate 1

This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]

C7ORF77 Gene

chromosome 7 open reading frame 77

C7ORF76 Gene

chromosome 7 open reading frame 76

C1ORF53 Gene

chromosome 1 open reading frame 53

C1ORF52 Gene

chromosome 1 open reading frame 52

C1ORF50 Gene

chromosome 1 open reading frame 50

C1ORF56 Gene

chromosome 1 open reading frame 56

C1ORF54 Gene

chromosome 1 open reading frame 54

C18ORF21 Gene

chromosome 18 open reading frame 21

C18ORF25 Gene

chromosome 18 open reading frame 25

HBFQTL4 Gene

Fetal hemoglobin QTL on chromosome 8

DEL15Q24 Gene

Chromosome 15q24 deletion syndrome

LOC390314 Gene

chromosome 20 open reading frame 27 pseudogene

C16DELQ22 Gene

Chromosome 16q22 deletion syndrome

C7ORF25 Gene

chromosome 7 open reading frame 25

C7ORF26 Gene

chromosome 7 open reading frame 26

LOC100129168 Gene

chromosome 6 open reading frame 203 pseudogene

C6ORF62 Gene

chromosome 6 open reading frame 62

DEL15Q13.3 Gene

Chromosome 15q13.3 microdeletion syndrome

C12ORF29 Gene

chromosome 12 open reading frame 29

DEL5Q12 Gene

Chromosome 5q12 deletion sydrome

C19ORF70 Gene

chromosome 19 open reading frame 70

C19ORF73 Gene

chromosome 19 open reading frame 73

CXORF40A Gene

chromosome X open reading frame 40A

CXORF40B Gene

chromosome X open reading frame 40B

DUP1Q21 Gene

Chromosome 1q21.1 duplication syndrome

C2ORF50 Gene

chromosome 2 open reading frame 50

C2ORF57 Gene

chromosome 2 open reading frame 57

C2ORF54 Gene

chromosome 2 open reading frame 54

LOC645086 Gene

chromosome 11 open reading frame 58 pseudogene

WBSCR2 Gene

Williams-Beuren syndrome chromosome region 2

C14ORF177 Gene

chromosome 14 open reading frame 177

C14ORF178 Gene

chromosome 14 open reading frame 178

C16ORF95 Gene

chromosome 16 open reading frame 95

LOC100129254 Gene

chromosome 3 open reading frame 38 pseudogene

C2ORF27AP2 Gene

chromosome 2 open reading frame 27A pseudogene 2

C2ORF27AP3 Gene

chromosome 2 open reading frame 27A pseudogene 3

C2ORF27AP1 Gene

chromosome 2 open reading frame 27A pseudogene 1

XIC Gene

X chromosome inactivation center

C1ORF210 Gene

chromosome 1 open reading frame 210

C1ORF216 Gene

chromosome 1 open reading frame 216

C17ORF62 Gene

chromosome 17 open reading frame 62

C17ORF64 Gene

chromosome 17 open reading frame 64

C17ORF67 Gene

chromosome 17 open reading frame 67

C18ORF8 Gene

chromosome 18 open reading frame 8

This gene encodes a colon cancer associated protein. [provided by RefSeq, Jan 2013]

LOC646970 Gene

chromosome 5 open reading frame 15 pseudogene

LOC100132762 Gene

chromosome 17 open reading frame 80 pseudogene

RSCIS Gene

Radiation sensitivity/chromosome instability syndrome, autosomal dominant

C5ORF58 Gene

chromosome 5 open reading frame 58

C5ORF56 Gene

chromosome 5 open reading frame 56

C5ORF52 Gene

chromosome 5 open reading frame 52

C5ORF51 Gene

chromosome 5 open reading frame 51

C1ORF86 Gene

chromosome 1 open reading frame 86

C1ORF87 Gene

chromosome 1 open reading frame 87

CXORF36 Gene

chromosome X open reading frame 36

C8ORF17 Gene

chromosome 8 open reading frame 17

C4ORF19 Gene

chromosome 4 open reading frame 19

C4ORF17 Gene

chromosome 4 open reading frame 17

C3ORF84 Gene

chromosome 3 open reading frame 84

CXORF38 Gene

chromosome X open reading frame 38

LOC100129989 Gene

chromosome 12 open reading frame 29 pseudogene

C9ORF16 Gene

chromosome 9 open reading frame 16

LOC100420859 Gene

chromosome 2 open reading frame 69 pseudogene

C16ORF62 Gene

chromosome 16 open reading frame 62

C20ORF78 Gene

chromosome 20 open reading frame 78

C3ORF80 Gene

chromosome 3 open reading frame 80

DEL1P36 Gene

Chromosome 1p36 deletion syndrome

C11ORF24 Gene

chromosome 11 open reading frame 24

LOC100130455 Gene

chromosome 20 open reading frame 196 pseudogene

C10ORF67 Gene

chromosome 10 open reading frame 67

C10ORF62 Gene

chromosome 10 open reading frame 62

C6ORF229 Gene

chromosome 6 open reading frame 229

C6ORF222 Gene

chromosome 6 open reading frame 222

C6ORF223 Gene

chromosome 6 open reading frame 223

C6ORF226 Gene

chromosome 6 open reading frame 226

C9ORF171 Gene

chromosome 9 open reading frame 171

C9ORF170 Gene

chromosome 9 open reading frame 170

C1ORF162 Gene

chromosome 1 open reading frame 162

C1ORF167 Gene

chromosome 1 open reading frame 167

GTSCR1 Gene

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

C1ORF168 Gene

chromosome 1 open reading frame 168

LOC100526840 Gene

chromosome 18 open reading frame 32 pseudogene

C2ORF83 Gene

chromosome 2 open reading frame 83

C18ORF12 Gene

chromosome 18 open reading frame 12

LOC389705 Gene

chromosome 4 open reading frame 27 pseudogene

DEL7Q11.23 Gene

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

C9ORF91 Gene

chromosome 9 open reading frame 91

LOC100289196 Gene

chromosome 7 open reading frame 73 pseudogene

C12ORF57 Gene

chromosome 12 open reading frame 57

This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

C12ORF54 Gene

chromosome 12 open reading frame 54

DUP17Q21.31 Gene

Chromosome 17q21.31 duplication syndrome

C19ORF40 Gene

chromosome 19 open reading frame 40

FAAP24 is a component of the Fanconi anemia (FA) core complex (see MIM 227650), which plays a crucial role in DNA damage response (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008]

C19ORF43 Gene

chromosome 19 open reading frame 43

C19ORF45 Gene

chromosome 19 open reading frame 45

C19ORF47 Gene

chromosome 19 open reading frame 47

C19ORF48 Gene

chromosome 19 open reading frame 48

C6ORF118 Gene

chromosome 6 open reading frame 118

C2ORF61 Gene

chromosome 2 open reading frame 61

C2ORF69 Gene

chromosome 2 open reading frame 69

C2ORF68 Gene

chromosome 2 open reading frame 68

LOC100128808 Gene

chromosome 11 open reading frame 51 pseudogene

LOC100420925 Gene

chromosome 2 open reading frame 27A pseudogene

C7ORF55 Gene

chromosome 7 open reading frame 55

C7ORF57 Gene

chromosome 7 open reading frame 57

C7ORF50 Gene

chromosome 7 open reading frame 50

C14ORF142 Gene

chromosome 14 open reading frame 142

C14ORF144 Gene

chromosome 14 open reading frame 144

DEL19Q13.11 Gene

Chromosome 19q13.11 deletion syndrome

LOC100288558 Gene

chromosome 4 open reading frame 46 pseudogene

LOC100420770 Gene

chromosome 12 open reading frame 10 pseudogene

LOC100420779 Gene

chromosome 16 open reading frame 70 pseudogene

LOC100420778 Gene

chromosome 2 open reading frame 27A pseudogene

C14ORF80 Gene

chromosome 14 open reading frame 80

C15ORF48 Gene

chromosome 15 open reading frame 48

This gene was first identified in a study of human esophageal squamous cell carcinoma tissues. Levels of both the message and protein are reduced in carcinoma samples. In adult human tissues, this gene is expressed in the the esophagus, stomach, small intestine, colon and placenta. Alternatively spliced transcript variants that encode the same protein have been identified. [provided by RefSeq, Jun 2012]

C15ORF40 Gene

chromosome 15 open reading frame 40

C15ORF43 Gene

chromosome 15 open reading frame 43

C21ORF91 Gene

chromosome 21 open reading frame 91

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]

C8ORF60 Gene

chromosome 8 open reading frame 60

LOC100287212 Gene

chromosome 4 open reading frame 3 pseudogene

C4ORF50 Gene

chromosome 4 open reading frame 50

C10ORF131 Gene

chromosome 10 open reading frame 131

OTDD Gene

Otodental dysplasia chromosome deletion syndrome

DEL17Q11.2 Gene

chromosome 17q11.2 deletion syndrome

LOC100125409 Gene

chromosome 4 open reading frame 27 pseudogene

LOC399815 Gene

chromosome 10 open reading frame 88 pseudogene

C15ORF62 Gene

chromosome 15 open reading frame 62

AMLCR2 Gene

acute myeloid leukemia chromosome region 2

C16ORF13 Gene

chromosome 16 open reading frame 13

DUP8Q22.1 Gene

Leri pleonosteosis chromosome duplication syndrome

C11ORF21 Gene

chromosome 11 open reading frame 21

C4ORF3 Gene

chromosome 4 open reading frame 3

C11ORF71 Gene

chromosome 11 open reading frame 71

C11ORF70 Gene

chromosome 11 open reading frame 70

C11ORF73 Gene

chromosome 11 open reading frame 73

C11ORF74 Gene

chromosome 11 open reading frame 74

This gene encodes a protein that was identified as a cellular interacting partner of non-structural protein 10 of the severe acute respiratory syndrome coronavirus (SARS-CoV). The encoded protein may function as a negative regulator of transcription. There is a pseudogene for this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]

HDLCQ2 Gene

High density lipoprotein cholesterol level QTL on chromosome 8

C10ORF54 Gene

chromosome 10 open reading frame 54

C10ORF53 Gene

chromosome 10 open reading frame 53

DEL4Q21 Gene

Chromosome 4q21 deletion syndrome

DUP22Q13 Gene

Chromosome 22q13 duplication syndrome

GCY Gene

growth control, Y chromosome influenced

C9ORF147 Gene

chromosome 9 open reading frame 147

C9ORF142 Gene

chromosome 9 open reading frame 142

C1ORF131 Gene

chromosome 1 open reading frame 131

C1ORF134 Gene

chromosome 1 open reading frame 134

C1ORF137 Gene

chromosome 1 open reading frame 137

LOC100420789 Gene

chromosome 2 open reading frame 27A pseudogene

C3ORF33 Gene

chromosome 3 open reading frame 33

C3ORF30 Gene

chromosome 3 open reading frame 30

C3ORF36 Gene

chromosome 3 open reading frame 36

C3ORF35 Gene

chromosome 3 open reading frame 35

C3ORF38 Gene

chromosome 3 open reading frame 38

LOC644462 Gene

amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 2 pseudogene

LOC389473 Gene

chromosome 5 open reading frame 13 pseudogene

C20ORF203 Gene

chromosome 20 open reading frame 203

C20ORF202 Gene

chromosome 20 open reading frame 202

C9ORF40 Gene

chromosome 9 open reading frame 40

C9ORF41 Gene

chromosome 9 open reading frame 41

C9ORF43 Gene

chromosome 9 open reading frame 43

C9ORF47 Gene

chromosome 9 open reading frame 47

C16ORF96 Gene

chromosome 16 open reading frame 96

C16ORF97 Gene

chromosome 16 open reading frame 97

C16ORF92 Gene

chromosome 16 open reading frame 92

C16ORF93 Gene

chromosome 16 open reading frame 93

C16ORF90 Gene

chromosome 16 open reading frame 90

C16ORF91 Gene

chromosome 16 open reading frame 91

LOC729930 Gene

chromosome 11 open reading frame 74 pseudogene

DEL17P13.1 Gene

Chromosome 17p13.1 deletion syndrome

C12ORF80 Gene

chromosome 12 open reading frame 80

DEL11P15P14 Gene

Chromosome 11p15-p14 deletion syndrome

C6ORF141 Gene

chromosome 6 open reading frame 141

DEL1Q21 Gene

Chromosome 1q21.1 deletion syndrome

C1ORF74 Gene

chromosome 1 open reading frame 74

C2ORF72 Gene

chromosome 2 open reading frame 72

C18ORF42 Gene

chromosome 18 open reading frame 42

C9ORF78 Gene

chromosome 9 open reading frame 78

NHP2L1 Gene

NHP2 non-histone chromosome protein 2-like 1 (S. cerevisiae)

Originally named because of its sequence similarity to the Saccharomyces cerevisiae NHP2 (non-histone protein 2), this protein appears to be a highly conserved nuclear protein that is a component of the [U4/U6.U5] tri-snRNP. It binds to the 5' stem-loop of U4 snRNA. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

C1ORF220 Gene

chromosome 1 open reading frame 220

C1ORF229 Gene

chromosome 1 open reading frame 229

C9ORF173 Gene

chromosome 9 open reading frame 173

C6ORF48 Gene

chromosome 6 open reading frame 48

C6ORF47 Gene

chromosome 6 open reading frame 47

chromosome 8p11 myeloproliferative syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 8p11 myeloproliferative syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

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

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations; sex chromosome disorders of sex development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic 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.

Transient Myeloproliferative Disorder of Down Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Transient Myeloproliferative Disorder of Down Syndrome from the curated CTD Gene-Disease Associations dataset.

Myeloproliferative Syndrome, Transient Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myeloproliferative Syndrome, Transient from the curated CTD 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.

budd-chiari syndrome; myeloproliferative disorders; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease budd-chiari syndrome; myeloproliferative disorders; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

budd-chiari syndrome; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease budd-chiari syndrome; myeloproliferative disorders 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.

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.

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma 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.

proximal chromosome 9p to q and distal chromosome 9q Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; chromosome deletion; infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

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

ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ahg deficiency disease; chromosome inversion; hemophilia a; hemorrhage; inversion, chromosome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms 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.

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; neoplasms Gene Set

From GAD Gene-Disease Associations

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

chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; hemochromatosis; inversion, chromosome; iron overload; thalassemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadasil; chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set

From GAD Gene-Disease Associations

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

aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn 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.

homologous chromosome movement towards spindle pole involved in homologous chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the homologous chromosome movement towards spindle pole involved in homologous chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

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

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Myeloproliferative Disorders Gene Set

From CTD Gene-Disease Associations

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

Myeloproliferative Disorder, Chronic, with Eosinophilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myeloproliferative Disorder, Chronic, with Eosinophilia from the curated CTD Gene-Disease Associations dataset.

Myelodysplastic-Myeloproliferative Diseases Gene Set

From CTD Gene-Disease Associations

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

Myeloproliferative Disorders Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Myeloproliferative Disorders in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

chronic myeloproliferative disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

myelodysplastic myeloproliferative cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

chronic myeloproliferative disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemorrhage; myeloproliferative disorders; thrombosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma; myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; venous thrombosis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombocythemia, essential; thrombocythemia, hemorrhagic; thrombosis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential; thrombocythemia, hemorrhagic 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.

genomic instability; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

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

arterial occlusive diseases; myeloproliferative disorders; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arterial occlusive diseases; myeloproliferative disorders; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disease Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; polycythemia; polycythemia vera; thrombocythemia, essential; thrombocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential 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.

hematologic neoplasms; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative neoplasms Gene Set

From GAD Gene-Disease Associations

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

tumor progression of bcr/abl negative chronic myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tumor progression of bcr/abl negative chronic myeloproliferative disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombocytosis Gene Set

From GAD Gene-Disease Associations

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

iron overload; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; myeloproliferative disorders; thrombosis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; thrombosis Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; polycythemia vera Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; neoplasms; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

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

transient myeloproliferative disorder Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative disorders; neovascularization, pathologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloproliferative disorders; polycythemia vera; thrombocythemia, essential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloproliferative disorders; polycythemia vera; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blast crisis; blast phase; myeloproliferative disorders Gene Set

From GAD Gene-Disease Associations

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

myeloproliferative Gene Set

From GeneRIF Biological Term Annotations

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

Myeloproliferative neoplasms Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Myeloproliferative neoplasms phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

myelodysplastic myeloproliferative cancer Gene Set

From GWASdb SNP-Disease Associations

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

chronic myeloproliferative disease Gene Set

From GWASdb SNP-Disease Associations

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

myeloproliferative disorder Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the myeloproliferative disorder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

myeloproliferative disorder Gene Set

From HPO Gene-Disease Associations

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

Myeloproliferative Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

myeloproliferative disorder with eosinophilia Gene Set

From OMIM Gene-Disease Associations

genes associated with the myeloproliferative disorder with eosinophilia phenotype from the curated OMIM Gene-Disease Associations dataset.

myeloproliferative disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the myeloproliferative disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

Chromosome 2q32-q33 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 2q32-q33 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome 1q43-q44 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 1q43-q44 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome Xq28 deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome Xq28 deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome 9q deletion syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chromosome 9q deletion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chromosome 2q37 deletion syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome 2q37 deletion syndrome from the curated CTD Gene-Disease Associations dataset.

Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Chromosome Xp11.3 Deletion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome Xp11.3 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; digeorge syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome deletion; digeorge syndrome in GWAS and other genetic association datasets from the GAD 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.

down syndrome; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-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.

chromosome aberrations; li-fraumeni syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; li-fraumeni syndrome 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.

abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome 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.

chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q21.31 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q21.31 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 4q21 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 4q21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6pter-p24 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6pter-p24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q26-qter deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q26-qter deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xp11.23-p11.22 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xp11.23-p11.22 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q12 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q12 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 18p deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 18p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2p16.1-p15 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2p16.1-p15 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2p12-p11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2p12-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

leri pleonosteosis chromosome duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the leri pleonosteosis chromosome duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 7q11.23 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 7q11.23 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1p36 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1p36 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q21.1 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q21.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6q25-q25 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6q25-q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q11.2 deletion syndrome, 1.4mb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q11.2 deletion syndrome, 1.4mb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q25 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q25 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1p32-p31 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1p32-p31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 22q11.2 deletion syndrome, distal Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p11.2 deletion syndrome, 593kb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p11.2 deletion syndrome, 593kb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q13.3 microdeletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q13.3 microdeletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p11.2 deletion syndrome, 220kb Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p11.2 deletion syndrome, 220kb phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 11p15-p14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 11p15-p14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xq28 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xq28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q23.1-q23.2 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q23.1-q23.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 22q13 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 22q13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p12.2-p11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p12.2-p11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p11.2 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p11.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xp11.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xp11.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p13.3 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 22q11.2 microduplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 22q11.2 microduplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16q22 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xq27.3-q28 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xq27.3-q28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 18q deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 18q deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 8q21.11 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 8q21.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 16p13.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 16p13.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17p13.3 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2q31.1 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2q31.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

radiation sensitivity/chromosome instability syndrome, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the radiation sensitivity/chromosome instability syndrome, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q43-q44 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q43-q44 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 13q14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 13q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 2q31.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 2q31.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 6q11-q14 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 6q11-q14 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q21.1 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q21.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q11.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q11.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 3q29 microduplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 3q29 microduplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 3q13.31 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 3q13.31 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 4q32.1-q32.2 triplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 4q32.1-q32.2 triplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 9p deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 9p deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q12 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q12 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome xp21 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome xp21 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 19p13.13 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 19p13.13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 1q41-q42 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 1q41-q42 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 10q26 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 10q26 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 5p13 duplication syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 5p13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 15q24 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 15q24 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 19p13.13 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 19p13.13 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17q23.1-q23.2 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17q23.1-q23.2 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 19q13.11 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 19q13.11 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 14q11-q22 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 14q11-q22 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 3q29 microdeletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 3q29 microdeletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 17p13.1 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 17p13.1 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

chromosome 5q14.3 deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the chromosome 5q14.3 deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders 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.

insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

cytoplasmic chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cytoplasmic chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

sex chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the sex chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome inner kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome inner kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome outer kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome, centromeric core domain Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome, centromeric core domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear chromosome part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear chromosome part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

y chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the y chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear chromosome, telomeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome, telomeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

x chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the x chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome passenger complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome passenger complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome outer kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome outer kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cytoplasmic chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cytoplasmic chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

sex chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the sex chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome inner kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome inner kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed nuclear chromosome kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed nuclear chromosome outer kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polytene chromosome chromocenter Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polytene chromosome chromocenter cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed nuclear chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polytene chromosome puff Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polytene chromosome puff cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

w chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the w chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chloroplast chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chloroplast chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

y chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the y chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nuclear chromosome part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear chromosome part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polytene chromosome interband Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polytene chromosome interband cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plastid chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plastid chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nuclear chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

z chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the z chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome segregation-directing complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome segregation-directing complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nuclear chromosome, telomeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polytene chromosome band Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polytene chromosome band cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome, telomeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

x chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the x chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

polytene chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the polytene chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome passenger complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome passenger complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome outer kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome outer kinetochore cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed nuclear chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Chromosome 17 deletion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome 17 deletion from the curated CTD Gene-Disease Associations dataset.

Chromosome Breakage Gene Set

From CTD Gene-Disease Associations

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

TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TUMOR SUPPRESSOR GENE ON CHROMOSOME 11 from the curated CTD Gene-Disease Associations dataset.

Chromosome Disorders Gene Set

From CTD Gene-Disease Associations

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

Frontotemporal Dementia, Chromosome 3-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Frontotemporal Dementia, Chromosome 3-Linked from the curated CTD Gene-Disease Associations dataset.

Chromosome Aberrations Gene Set

From CTD Gene-Disease Associations

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

Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.

Micronuclei, Chromosome-Defective Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Micronuclei, Chromosome-Defective from the curated CTD Gene-Disease Associations dataset.

Chromosome 3, monosomy 3p25 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chromosome 3, monosomy 3p25 from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, Associated With Chromosome 5q Deletion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Associated With Chromosome 5q Deletion from the curated CTD Gene-Disease Associations dataset.

chromosome aberrations; neoplasms Gene Set

From GAD Gene-Disease Associations

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

increased chromosome aberrations and higher lung cancer risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased chromosome aberrations and higher lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; chromosome deletion; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; infertility, male Gene Set

From GAD Gene-Disease Associations

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

infertility, male; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

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

micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

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

amyotrophic lateral sclerosis; chromosome disorders; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyotrophic lateral sclerosis; chromosome disorders; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; chromosome deletion; head and neck neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; chromosome breakage; dna damage; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; intestinal neoplasms; lymphoma; lymphoma, b-cell, marginal zone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; infertility, male Gene Set

From GAD Gene-Disease Associations

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

breast neoplasms; chromosome breakage; mammary neoplasms Gene Set

From GAD Gene-Disease Associations

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

chromosome deletion Gene Set

From GAD Gene-Disease Associations

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

brill-symmers disease; chromosome deletion; lymphoma, follicular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; chromosome deletion; lymphoma, follicular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

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

adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; biliary tract neoplasm; biliary tract neoplasms; chromosome deletion; diabetes complications; pancreatic neoplasm; pancreatic neoplasms 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.

chromosome inversion; hemophilia a Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; hemophilia a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

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

dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; lung neoplasms; micronuclei, chromosome-defective; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome disorders; fam hyperbetalipoproteinaemia; hyperlipoproteinemia type ii in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; epilepsy, generalized; Gene Set

From GAD Gene-Disease Associations

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

chromosome disorders; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome disorders; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diseases in twins; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

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

altitude sickness; chromosome deletion; pulmonary edema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease altitude sickness; chromosome deletion; pulmonary edema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

azoospermia; chromosome deletion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease azoospermia; chromosome deletion 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.

carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; dna damage Gene Set

From GAD Gene-Disease Associations

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

carcinoma, squamous cell; chromosome breakage; head and neck neoplasms Gene Set

From GAD Gene-Disease Associations

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

fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; nondisjunction, genetic; sex chromosome aberrations; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; chromosome aberrations; lung neoplasms Gene Set

From GAD Gene-Disease Associations

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

flushing; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease flushing; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome breakage Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations Gene Set

From GAD Gene-Disease Associations

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

chromosome breakage; leukemia, myelogenous, chronic, bcr-abl positive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome breakage; leukemia, myelogenous, chronic, bcr-abl positive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; keratosis Gene Set

From GAD Gene-Disease Associations

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

colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colitis, ulcerative; crohn disease; genetic diseases, x-linked; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cd3 epsilon locus on chromosome 11 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cd3 epsilon locus on chromosome 11 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; chromosome inversion; Gene Set

From GAD Gene-Disease Associations

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

chromosome breakage; cleft lip; cleft palate; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome breakage; cleft lip; cleft palate; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, male; oligospermia; sex chromosome aberrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, male; oligospermia; sex chromosome aberrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome deletion; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

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

chromosome Gene Set

From GeneRIF Biological Term Annotations

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

chromosome separation Gene Set

From GO Biological Process Annotations

genes participating in the chromosome separation biological process from the curated GO Biological Process Annotations dataset.

mitotic chromosome movement towards spindle pole Gene Set

From GO Biological Process Annotations

genes participating in the mitotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations dataset.

random inactivation of x chromosome Gene Set

From GO Biological Process Annotations

genes participating in the random inactivation of x chromosome biological process from the curated GO Biological Process Annotations dataset.

meiotic chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the meiotic chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

chromosome movement towards spindle pole Gene Set

From GO Biological Process Annotations

genes participating in the chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations dataset.

meiotic chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the meiotic chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

apoptotic chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

chromosome organization Gene Set

From GO Biological Process Annotations

genes participating in the chromosome organization biological process from the curated GO Biological Process Annotations dataset.

establishment of chromosome localization Gene Set

From GO Biological Process Annotations

genes participating in the establishment of chromosome localization biological process from the curated GO Biological Process Annotations dataset.

establishment of protein localization to chromosome Gene Set

From GO Biological Process Annotations

genes participating in the establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations dataset.

chromosome attachment to the nuclear envelope Gene Set

From GO Biological Process Annotations

genes participating in the chromosome attachment to the nuclear envelope biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of protein localization to chromosome Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of protein localization to chromosome biological process from the curated GO Biological Process Annotations dataset.

mitotic chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the mitotic chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

chromosome passenger complex localization to kinetochore Gene Set

From GO Biological Process Annotations

genes participating in the chromosome passenger complex localization to kinetochore biological process from the curated GO Biological Process Annotations dataset.

chromosome passenger complex localization to spindle midzone Gene Set

From GO Biological Process Annotations

genes participating in the chromosome passenger complex localization to spindle midzone biological process from the curated GO Biological Process Annotations dataset.

protein localization to chromosome, centromeric region Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to chromosome, centromeric region biological process from the curated GO Biological Process Annotations dataset.

chromosome organization involved in meiosis Gene Set

From GO Biological Process Annotations

genes participating in the chromosome organization involved in meiosis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of chromosome organization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of chromosome organization biological process from the curated GO Biological Process Annotations dataset.

negative regulation of chromosome organization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of chromosome organization biological process from the curated GO Biological Process Annotations dataset.

regulation of chromosome organization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of chromosome organization biological process from the curated GO Biological Process Annotations dataset.

regulation of chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

regulation of homologous chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of homologous chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

histone h3-s10 phosphorylation involved in chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the histone h3-s10 phosphorylation involved in chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

inactivation of x chromosome by dna methylation Gene Set

From GO Biological Process Annotations

genes participating in the inactivation of x chromosome by dna methylation biological process from the curated GO Biological Process Annotations dataset.

meiotic chromosome movement towards spindle pole Gene Set

From GO Biological Process Annotations

genes participating in the meiotic chromosome movement towards spindle pole biological process from the curated GO Biological Process Annotations dataset.

homologous chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the homologous chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

dosage compensation by inactivation of x chromosome Gene Set

From GO Biological Process Annotations

genes participating in the dosage compensation by inactivation of x chromosome biological process from the curated GO Biological Process Annotations dataset.

meiotic chromosome separation Gene Set

From GO Biological Process Annotations

genes participating in the meiotic chromosome separation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

male meiosis chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

male meiosis chromosome separation Gene Set

From GO Biological Process Annotations

genes participating in the male meiosis chromosome separation biological process from the curated GO Biological Process Annotations dataset.

regulation of chromosome segregation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of chromosome segregation biological process from the curated GO Biological Process Annotations dataset.

chromosome breakage Gene Set

From GO Biological Process Annotations

genes participating in the chromosome breakage biological process from the curated GO Biological Process Annotations dataset.

chromosome condensation Gene Set

From GO Biological Process Annotations

genes participating in the chromosome condensation biological process from the curated GO Biological Process Annotations dataset.

histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore Gene Set

From GO Biological Process Annotations

genes participating in the histone h3-t3 phosphorylation involved in chromosome passenger complex localization to kinetochore biological process from the curated GO Biological Process Annotations dataset.

protein localization to chromosome Gene Set

From