abnormal spermatogonia morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the large unspecialized male germ cells that give rise to spermatocytes (Mammalian Phenotype Ontology, MP_0006378)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006378
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Genes

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

Symbol Name
ACVR2A activin A receptor, type IIA
APAF1 apoptotic peptidase activating factor 1
CCDC169-SOHLH2 CCDC169-SOHLH2 readthrough
CIRBP cold inducible RNA binding protein
DHH desert hedgehog
DMRTC2 DMRT-like family C2
EHD1 EH-domain containing 1
ETV5 ets variant 5
FANCM Fanconi anemia, complementation group M
FSHB follicle stimulating hormone, beta polypeptide
FSHR follicle stimulating hormone receptor
HELQ helicase, POLQ-like
HMGA2 high mobility group AT-hook 2
JMJD1C jumonji domain containing 1C
MCM9 minichromosome maintenance complex component 9
NXF2 nuclear RNA export factor 2
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PHYH phytanoyl-CoA 2-hydroxylase
PIWIL2 piwi-like RNA-mediated gene silencing 2
RAD18 RAD18 E3 ubiquitin protein ligase
RANBP9 RAN binding protein 9
RNF8 ring finger protein 8, E3 ubiquitin protein ligase
TDRD9 tudor domain containing 9
USP1 ubiquitin specific peptidase 1
ZBTB16 zinc finger and BTB domain containing 16