abnormal seminal vesicle weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the weight of one or both of the two folded, sac shaped, glands that is a diverticulum of the ductus deferens (Mammalian Phenotype Ontology, MP_0004908)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004908
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Genes

30 gene mutations causing the abnormal seminal vesicle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AFF4 AF4/FMR2 family, member 4
AHR aryl hydrocarbon receptor
AKAP9 A kinase (PRKA) anchor protein 9
AR androgen receptor
BCL2L2 BCL2-like 2
BCO2 beta-carotene oxygenase 2
BGLAP bone gamma-carboxyglutamate (gla) protein
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CHST8 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8
CXCR2 chemokine (C-X-C motif) receptor 2
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DFNB31 deafness, autosomal recessive 31
FKBP4 FK506 binding protein 4, 59kDa
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
GPRC6A G protein-coupled receptor, class C, group 6, member A
KISS1R KISS1 receptor
LEP leptin
LHCGR luteinizing hormone/choriogonadotropin receptor
MARK2 MAP/microtubule affinity-regulating kinase 2
NR5A2 nuclear receptor subfamily 5, group A, member 2
PLAG1 pleiomorphic adenoma gene 1
PRL prolactin
PRLR prolactin receptor
PSAP prosaposin
PTH2 parathyroid hormone 2
STX2 syntaxin 2
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1
VGF VGF nerve growth factor inducible
VIP vasoactive intestinal peptide