abnormality of multiple cell lineages in the bone marrow Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012145
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68 genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATR ATR serine/threonine kinase
BRAF B-Raf proto-oncogene, serine/threonine kinase
BRCA2 breast cancer 2, early onset
BRIP1 BRCA1 interacting protein C-terminal helicase 1
CALR calreticulin
CD27 CD27 molecule
CLCN7 chloride channel, voltage-sensitive 7
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
CTC1 CTS telomere maintenance complex component 1
DHFR dihydrofolate reductase
DKC1 dyskeratosis congenita 1, dyskerin
ERCC4 excision repair cross-complementation group 4
ERCC6L2 excision repair cross-complementation group 6-like 2
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FANCF Fanconi anemia, complementation group F
FANCG Fanconi anemia, complementation group G
FANCI Fanconi anemia, complementation group I
FANCL Fanconi anemia, complementation group L
FANCM Fanconi anemia, complementation group M
GATA2 GATA binding protein 2
GBA glucosidase, beta, acid
GFI1B growth factor independent 1B transcription repressor
HBB hemoglobin, beta
HOXA11 homeobox A11
IGHV4-34 immunoglobulin heavy variable 4-34
ITK IL2-inducible T-cell kinase
IVD isovaleryl-CoA dehydrogenase
JAK2 Janus kinase 2
LBR lamin B receptor
LIG4 ligase IV, DNA, ATP-dependent
LMBRD1 LMBR1 domain containing 1
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MPL MPL proto-oncogene, thrombopoietin receptor
NBEAL2 neurobeachin-like 2
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PALB2 partner and localizer of BRCA2
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PSTPIP1 proline-serine-threonine phosphatase interacting protein 1
RAB27A RAB27A, member RAS oncogene family
RAB40AL RAB40A, member RAS oncogene family-like
RAD51C RAD51 paralog C
RNASEH2A ribonuclease H2, subunit A
RTEL1 regulator of telomere elongation helicase 1
SBDS Shwachman-Bodian-Diamond syndrome
SCARB2 scavenger receptor class B, member 2
SH2B3 SH2B adaptor protein 3
SH2D1A SH2 domain containing 1A
SLC46A1 solute carrier family 46 (folate transporter), member 1
SLX4 SLX4 structure-specific endonuclease subunit
SRP72 signal recognition particle 72kDa
TBXAS1 thromboxane A synthase 1 (platelet)
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TCN2 transcobalamin II
TERC telomerase RNA component
TERT telomerase reverse transcriptase
TGFB1 transforming growth factor, beta 1
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
USB1 U6 snRNA biogenesis 1
WDR19 WD repeat domain 19
WRAP53 WD repeat containing, antisense to TP53