abnormal number of erythroid precursors Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviation from the normal count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow. (Human Phenotype Ontology, HP_0012131)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012131
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9 genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C15ORF41 chromosome 15 open reading frame 41
CDAN1 codanin 1
G6PC3 glucose 6 phosphatase, catalytic, 3
GIF gastric intrinsic factor (vitamin B synthesis)
KLF1 Kruppel-like factor 1 (erythroid)
PUS1 pseudouridylate synthase 1
RPL35A ribosomal protein L35a
RPS14 ribosomal protein S14
RPS17 ribosomal protein S17