thin endometrium Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	reduced thickness of the glandular mucous membrane lining of the uterine cavity that is hormonally responsive during the estrous/menstrual cycle and during pregnancy (Mammalian Phenotype Ontology, MP_0008258)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008258
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Genes

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

Symbol	Name
BMPR1B	bone morphogenetic protein receptor, type IB
CYP19A1	cytochrome P450, family 19, subfamily A, polypeptide 1
HOXA11	homeobox A11
IGF2R	insulin-like growth factor 2 receptor
LHB	luteinizing hormone beta polypeptide
LHCGR	luteinizing hormone/choriogonadotropin receptor
NPC1	Niemann-Pick disease, type C1
NPR2	natriuretic peptide receptor 2