Erythroid Hypoplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Decreased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow. (Human Phenotype Ontology, HP_0012133)
External Link https://www.disgenet.org/browser/0/1/0/C0542035
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Genes

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

Symbol Name
CNBP CCHC-type zinc finger, nucleic acid binding protein
FAM69A family with sequence similarity 69, member A
FANCB Fanconi anemia, complementation group B
G6PC3 glucose 6 phosphatase, catalytic, 3
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase
MTUS1 microtubule associated tumor suppressor 1
RPL35A ribosomal protein L35a
RPL5 ribosomal protein L5
RPS14 ribosomal protein S14
RPS15A ribosomal protein S15a
RPS17 ribosomal protein S17
RPS19 ribosomal protein S19
TET2 tet methylcytosine dioxygenase 2
TP53 tumor protein p53