abnormal male reproductive gland physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of any sex gland that is part of the male reproductive system (Mammalian Phenotype Ontology, MP_0013327)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013327
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Genes

31 gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACSBG1 acyl-CoA synthetase bubblegum family member 1
ADRA1B adrenoceptor alpha 1B
AIRE autoimmune regulator
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CELF1 CUGBP, Elav-like family member 1
CSF1 colony stimulating factor 1 (macrophage)
CSF1R colony stimulating factor 1 receptor
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
FADS2 fatty acid desaturase 2
FSHR follicle stimulating hormone receptor
GAL galanin/GMAP prepropeptide
GHR growth hormone receptor
GSX1 GS homeobox 1
HOXB13 homeobox B13
HTR3A 5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
KIF1C kinesin family member 1C
LDHC lactate dehydrogenase C
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LHCGR luteinizing hormone/choriogonadotropin receptor
MEI4 meiosis-specific 4 homolog (S. cerevisiae)
NKX2-1 NK2 homeobox 1
NKX3-1 NK3 homeobox 1
NR0B2 nuclear receptor subfamily 0, group B, member 2
PLD6 phospholipase D family, member 6
SCRIB scribbled planar cell polarity protein
SIRT1 sirtuin 1
SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
STAT5A signal transducer and activator of transcription 5A
TMPRSS2 transmembrane protease, serine 2
TNF tumor necrosis factor
VIP vasoactive intestinal peptide