thin myometrium Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	reduced thickness of the smooth muscle coat of the uterus, which forms the main mass of the organ and surrounds and supports the endometrium (Mammalian Phenotype Ontology, MP_0008257)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008257
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Genes

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

Symbol	Name
CYP19A1	cytochrome P450, family 19, subfamily A, polypeptide 1
FANCL	Fanconi anemia, complementation group L
KPNA1	karyopherin alpha 1 (importin alpha 5)
LHCGR	luteinizing hormone/choriogonadotropin receptor
MEOX2	mesenchyme homeobox 2
NPC1	Niemann-Pick disease, type C1
NPR2	natriuretic peptide receptor 2
PAX8	paired box 8
WNT7A	wingless-type MMTV integration site family, member 7A