Atrophy Of Testis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0156312
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Genes

29 genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACBD3 acyl-CoA binding domain containing 3
AKR1A1 aldo-keto reductase family 1, member A1 (aldehyde reductase)
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial)
ANOS1 anosmin 1
AR androgen receptor
BMP2 bone morphogenetic protein 2
CASP3 caspase 3, apoptosis-related cysteine peptidase
CCL4 chemokine (C-C motif) ligand 4
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DMPK dystrophia myotonica-protein kinase
E2F1 E2F transcription factor 1
FSHB follicle stimulating hormone, beta polypeptide
HFE hemochromatosis
HIP1 huntingtin interacting protein 1
HMMR hyaluronan-mediated motility receptor (RHAMM)
HPRT1 hypoxanthine phosphoribosyltransferase 1
IGF1 insulin-like growth factor 1 (somatomedin C)
INPP5B inositol polyphosphate-5-phosphatase, 75kDa
IRS2 insulin receptor substrate 2
NABP2 nucleic acid binding protein 2
NHP2 NHP2 ribonucleoprotein
POLG polymerase (DNA directed), gamma
PRDX4 peroxiredoxin 4
SMS spermine synthase
SPSB1 splA/ryanodine receptor domain and SOCS box containing 1
TEX11 testis expressed 11
TP53 tumor protein p53
WFS1 Wolfram syndrome 1 (wolframin)