abnormal neutrophil cell number Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviation from the normal range of neutrophil cell counts in the circulation. (Human Phenotype Ontology, HP_0011991)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011991
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Genes

58 genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
AGA aspartylglucosaminidase
AP3B1 adaptor-related protein complex 3, beta 1 subunit
BLNK B-cell linker
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
CD79A CD79a molecule, immunoglobulin-associated alpha
CIITA class II, major histocompatibility complex, transactivator
CXCR4 chemokine (C-X-C motif) receptor 4
ELANE elastase, neutrophil expressed
FANCA Fanconi anemia, complementation group A
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FANCG Fanconi anemia, complementation group G
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FBXL4 F-box and leucine-rich repeat protein 4
FMO3 flavin containing monooxygenase 3
G6PC3 glucose 6 phosphatase, catalytic, 3
GATA1 GATA binding protein 1 (globin transcription factor 1)
GATA2 GATA binding protein 2
GFI1 growth factor independent 1 transcription repressor
GSS glutathione synthetase
HAX1 HCLS1 associated protein X-1
ICOS inducible T-cell co-stimulator
IGHM immunoglobulin heavy constant mu
JAGN1 jagunal homolog 1 (Drosophila)
LAMTOR2 late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
LBR lamin B receptor
LMBRD1 LMBR1 domain containing 1
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PGM3 phosphoglucomutase 3
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PNP purine nucleoside phosphorylase
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
RMRP RNA component of mitochondrial RNA processing endoribonuclease
RPS19 ribosomal protein S19
SBDS Shwachman-Bodian-Diamond syndrome
SLC35A1 solute carrier family 35 (CMP-sialic acid transporter), member A1
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
SLC46A1 solute carrier family 46 (folate transporter), member 1
SMARCAL1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
STK4 serine/threonine kinase 4
STX11 syntaxin 11
TAZ tafazzin
TCN2 transcobalamin II
USB1 U6 snRNA biogenesis 1
VPS13B vacuolar protein sorting 13 homolog B (yeast)
VPS45 vacuolar protein sorting 45 homolog (S. cerevisiae)
WAS Wiskott-Aldrich syndrome