abnormality of cells of the lymphoid lineage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of cells that originate from the lymphoid lineage restricted progenitor cell. (Human Phenotype Ontology, HP_0012140)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012140
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Genes

39 genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
AK2 adenylate kinase 2
ATM ATM serine/threonine kinase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CCBE1 collagen and calcium binding EGF domains 1
CD19 CD19 molecule
CD3D CD3d molecule, delta (CD3-TCR complex)
CD3E CD3e molecule, epsilon (CD3-TCR complex)
CD81 CD81 molecule
CHD7 chromodomain helicase DNA binding protein 7
CORO1A coronin, actin binding protein, 1A
CR2 complement component (3d/Epstein Barr virus) receptor 2
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FAT4 FAT atypical cadherin 4
G6PC3 glucose 6 phosphatase, catalytic, 3
ICOS inducible T-cell co-stimulator
IGHV4-34 immunoglobulin heavy variable 4-34
LMNB2 lamin B2
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
MS4A1 membrane-spanning 4-domains, subfamily A, member 1
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NHEJ1 nonhomologous end-joining factor 1
PGM3 phosphoglucomutase 3
PNP purine nucleoside phosphorylase
PRKCD protein kinase C, delta
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
STK4 serine/threonine kinase 4
TCN2 transcobalamin II
TERC telomerase RNA component
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C
TNFSF12 tumor necrosis factor (ligand) superfamily, member 12
UNC119 unc-119 homolog (C. elegans)
WAS Wiskott-Aldrich syndrome
ZBTB24 zinc finger and BTB domain containing 24