leydig cell hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005536
Similar Terms
Downloads & Tools

Genes

19 gene mutations causing the leydig cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACOX1 acyl-CoA oxidase 1, palmitoyl
AR androgen receptor
ARX aristaless related homeobox
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
BGLAP bone gamma-carboxyglutamate (gla) protein
CDK4 cyclin-dependent kinase 4
DHH desert hedgehog
EGR1 early growth response 1
FAM20C family with sequence similarity 20, member C
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
PLEKHA1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
PROKR2 prokineticin receptor 2
SGPL1 sphingosine-1-phosphate lyase 1
SH2B1 SH2B adaptor protein 1
SIRT1 sirtuin 1
WWOX WW domain containing oxidoreductase