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
Similar Terms
Downloads & Tools

Genes

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