abnormal female 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 female reproductive system (Mammalian Phenotype Ontology, MP_0013326)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013326
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Genes

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

Symbol Name
AHR aryl hydrocarbon receptor
ARID4A AT rich interactive domain 4A (RBP1-like)
CHST8 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
ESR1 estrogen receptor 1
FANCA Fanconi anemia, complementation group A
FOXC1 forkhead box C1
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GSX1 GS homeobox 1
HSF2 heat shock transcription factor 2
INHA inhibin, alpha
LHCGR luteinizing hormone/choriogonadotropin receptor
MCM9 minichromosome maintenance complex component 9
NOS3 nitric oxide synthase 3 (endothelial cell)
NPC1 Niemann-Pick disease, type C1
NR1H3 nuclear receptor subfamily 1, group H, member 3
PTGFR prostaglandin F receptor (FP)
RSPO1 R-spondin 1
ZGLP1 zinc finger, GATA-like protein 1