abnormal uterus development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal morphogenesis of the female muscular organ of gestation (Mammalian Phenotype Ontology, MP_0003572)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003572
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Genes

14 gene mutations causing the abnormal uterus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CSF1 colony stimulating factor 1 (macrophage)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
ESR1 estrogen receptor 1
KISS1 KiSS-1 metastasis-suppressor
KPNA1 karyopherin alpha 1 (importin alpha 5)
LHX3 LIM homeobox 3
PAX8 paired box 8
PGR progesterone receptor
SH2B1 SH2B adaptor protein 1
SPO11 SPO11 meiotic protein covalently bound to DSB
TIMP1 TIMP metallopeptidase inhibitor 1
WNT7A wingless-type MMTV integration site family, member 7A