Erythroid Hyperplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Increased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow. (Human Phenotype Ontology, HP_0012132)
External Link https://www.disgenet.org/browser/0/1/0/C0014800
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Genes

19 genes associated with the disease Erythroid Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C15ORF41 chromosome 15 open reading frame 41
CD177 CD177 molecule
CDAN1 codanin 1
ENTPD1 ectonucleoside triphosphate diphosphohydrolase 1
EPO erythropoietin
ERBB3 erb-b2 receptor tyrosine kinase 3
ERVW-1 endogenous retrovirus group W, member 1
FAM132B family with sequence similarity 132, member B
GH1 growth hormone 1
GLRX5 glutaredoxin 5
HAMP hepcidin antimicrobial peptide
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
IGF1 insulin-like growth factor 1 (somatomedin C)
JAK2 Janus kinase 2
KLF1 Kruppel-like factor 1 (erythroid)
PGF placental growth factor
PUS1 pseudouridylate synthase 1
TFR2 transferrin receptor 2