hematocrit Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The volume of packed RED BLOOD CELLS in a blood specimen. The volume is measured by centrifugation in a tube with graduated markings, or with automated blood cell counters. It is an indicator of erythrocyte status in disease. For example, ANEMIA shows a low value; POLYCYTHEMIA, a high value. (Experimental Factor Ontology, EFO_0004348)
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Genes

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

Symbol Name
ACOXL acyl-CoA oxidase-like
AGPAT4 1-acylglycerol-3-phosphate O-acyltransferase 4
ALX4 ALX homeobox 4
ATXN2 ataxin 2
BRE brain and reproductive organ-expressed (TNFRSF1A modulator)
C11ORF74 chromosome 11 open reading frame 74
C4ORF22 chromosome 4 open reading frame 22
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CAMK1D calcium/calmodulin-dependent protein kinase ID
CAMKMT calmodulin-lysine N-methyltransferase
CASP3 caspase 3, apoptosis-related cysteine peptidase
CELF5 CUGBP, Elav-like family member 5
CHN2 chimerin 2
CMTM8 CKLF-like MARVEL transmembrane domain containing 8
CSF3R colony stimulating factor 3 receptor (granulocyte)
CSMD1 CUB and Sushi multiple domains 1
CWC22 CWC22 spliceosome-associated protein
DLGAP1 discs, large (Drosophila) homolog-associated protein 1
DMD dystrophin
DPP6 dipeptidyl-peptidase 6
EML6 echinoderm microtubule associated protein like 6
EPB41L2 erythrocyte membrane protein band 4.1-like 2
ERG v-ets avian erythroblastosis virus E26 oncogene homolog
ESRRB estrogen-related receptor beta
EXT2 exostosin glycosyltransferase 2
FAM155A family with sequence similarity 155, member A
FAM19A5 family with sequence similarity 19 (chemokine (C-C motif)-like), member A5
FRAS1 Fraser extracellular matrix complex subunit 1
GALNS galactosamine (N-acetyl)-6-sulfatase
GPC6 glypican 6
GRIK4 glutamate receptor, ionotropic, kainate 4
HBS1L HBS1-like translational GTPase
HFE hemochromatosis
HK1 hexokinase 1
HPCAL1 hippocalcin-like 1
IL17A interleukin 17A
MACROD2 MACRO domain containing 2
MAP3K8 mitogen-activated protein kinase kinase kinase 8
MCM10 minichromosome maintenance complex component 10
MECOM MDS1 and EVI1 complex locus
MEGF10 multiple EGF-like-domains 10
MYB v-myb avian myeloblastosis viral oncogene homolog
NEDD1 neural precursor cell expressed, developmentally down-regulated 1
NKAIN2 Na+/K+ transporting ATPase interacting 2
NRG1 neuregulin 1
PACRG PARK2 co-regulated
PALLD palladin, cytoskeletal associated protein
PHACTR2 phosphatase and actin regulator 2
PHTF2 putative homeodomain transcription factor 2
PLCXD2 phosphatidylinositol-specific phospholipase C, X domain containing 2
PPEF2 protein phosphatase, EF-hand calcium binding domain 2
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PRKCE protein kinase C, epsilon
PTPRD protein tyrosine phosphatase, receptor type, D
RAG1 recombination activating gene 1
RFX8 RFX family member 8, lacking RFX DNA binding domain
SERGEF secretion regulating guanine nucleotide exchange factor
SH2B3 SH2B adaptor protein 3
SNX29 sorting nexin 29
SOX5 SRY (sex determining region Y)-box 5
TFR2 transferrin receptor 2
TMPRSS6 transmembrane protease, serine 6
WDR7 WD repeat domain 7