thin uterus Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness or depth of the female muscular organ of gestation (Mammalian Phenotype Ontology, MP_0009081)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009081
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Genes

8 gene mutations causing the thin uterus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CRTC1 CREB regulated transcription coactivator 1
FSHR follicle stimulating hormone receptor
GNRHR gonadotropin-releasing hormone receptor
LHCGR luteinizing hormone/choriogonadotropin receptor
NPC1 Niemann-Pick disease, type C1
WNT7A wingless-type MMTV integration site family, member 7A