abnormality of reticulocytes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reticulocyte abnormality. (Human Phenotype Ontology, HP_0004312)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004312
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Genes

28 genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
ANK1 ankyrin 1, erythrocytic
C15ORF41 chromosome 15 open reading frame 41
CDAN1 codanin 1
CLCN7 chloride channel, voltage-sensitive 7
FANCA Fanconi anemia, complementation group A
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
G6PD glucose-6-phosphate dehydrogenase
GATA1 GATA binding protein 1 (globin transcription factor 1)
HBG2 hemoglobin, gamma G
HK1 hexokinase 1
KLF1 Kruppel-like factor 1 (erythroid)
PFKM phosphofructokinase, muscle
PGK1 phosphoglycerate kinase 1
PIEZO1 piezo-type mechanosensitive ion channel component 1
PKLR pyruvate kinase, liver and RBC
RPL15 ribosomal protein L15
RPS17 ribosomal protein S17
RPS19 ribosomal protein S19
RPS24 ribosomal protein S24
SEC23B Sec23 homolog B (S. cerevisiae)
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
TCN2 transcobalamin II