autosomal genetic disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A monogenic disease that is caused by a mutation in a single gene on one of the non-sex chromosomes. (Human Disease Ontology, DOID_0050739)
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11 genes associated with the disease autosomal genetic disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HBG1 hemoglobin, gamma A 1.06123
HBS1L HBS1-like translational GTPase 0.790827
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein) 0.724323
APIP APAF1 interacting protein 0.63207
SLC22A23 solute carrier family 22, member 23 0.368757
CTH cystathionine gamma-lyase 0.327313
TSPYL4 TSPY-like 4 0.274608
AGTR2 angiotensin II receptor, type 2 0.197766
IFRD1 interferon-related developmental regulator 1 0.126165
AHRR aryl-hydrocarbon receptor repressor 0.126165
SLC8A3 solute carrier family 8 (sodium/calcium exchanger), member 3 0.052255