anemia, sickle cell Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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Genes

24 genes associated with the disease anemia, sickle cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
EPT1 ethanolaminephosphotransferase 1
GPM6B glycoprotein M6B
HBB hemoglobin, beta
HBS1L HBS1-like translational GTPase
KCNK6 potassium channel, two pore domain subfamily K, member 6
MBL2 mannose-binding lectin (protein C) 2, soluble
MCC mutated in colorectal cancers
MYB v-myb avian myeloblastosis viral oncogene homolog
PHEX phosphate regulating endopeptidase homolog, X-linked
SAR1A secretion associated, Ras related GTPase 1A
TOX thymocyte selection-associated high mobility group box
TRIM21 tripartite motif containing 21
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10
UGT1A3 UDP glucuronosyltransferase 1 family, polypeptide A3
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4
UGT1A5 UDP glucuronosyltransferase 1 family, polypeptide A5
UGT1A6 UDP glucuronosyltransferase 1 family, polypeptide A6
UGT1A7 UDP glucuronosyltransferase 1 family, polypeptide A7
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8
UGT1A9 UDP glucuronosyltransferase 1 family, polypeptide A9
UGT2B7 UDP glucuronosyltransferase 2 family, polypeptide B7