abnormal testis development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal morphogenesis of the male reproductive gland containing the germ cells (Mammalian Phenotype Ontology, MP_0003830)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003830
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23 gene mutations causing the abnormal testis development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
AKAP9 A kinase (PRKA) anchor protein 9
ATM ATM serine/threonine kinase
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CLCN2 chloride channel, voltage-sensitive 2
DHH desert hedgehog
DMRT1 doublesex and mab-3 related transcription factor 1
DMRTC2 DMRT-like family C2
FGF9 fibroblast growth factor 9
FSHR follicle stimulating hormone receptor
GADD45G growth arrest and DNA-damage-inducible, gamma
KIF18A kinesin family member 18A
KISS1 KiSS-1 metastasis-suppressor
LRP2 low density lipoprotein receptor-related protein 2
MAP3K4 mitogen-activated protein kinase kinase kinase 4
NR0B1 nuclear receptor subfamily 0, group B, member 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
PLEKHA1 pleckstrin homology domain containing, family A (phosphoinositide binding specific) member 1
SGPL1 sphingosine-1-phosphate lyase 1
SIRT1 sirtuin 1
SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
SMAD1 SMAD family member 1
TCF21 transcription factor 21