abnormal spermatogonia proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the proliferation of the spermatogonial stem cells either due to abnormal mitosis or apoptosis (Mammalian Phenotype Ontology, MP_0002685)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002685
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Genes

17 gene mutations causing the abnormal spermatogonia proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP8B bone morphogenetic protein 8b
CIRBP cold inducible RNA binding protein
CIT citron rho-interacting serine/threonine kinase
DAZAP1 DAZ associated protein 1
ETV5 ets variant 5
FSHR follicle stimulating hormone receptor
GAL3ST1 galactose-3-O-sulfotransferase 1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
NR1H2 nuclear receptor subfamily 1, group H, member 2
NXF2 nuclear RNA export factor 2
PATZ1 POZ (BTB) and AT hook containing zinc finger 1
RANBP9 RAN binding protein 9
TAF4B TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa
TSC22D3 TSC22 domain family, member 3
VRK1 vaccinia related kinase 1
ZBTB16 zinc finger and BTB domain containing 16
ZGLP1 zinc finger, GATA-like protein 1