abnormality of reticulocytes Gene Set
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
|
