abnormal uterine cervix morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the lower opening of the uterus to the vagina (Mammalian Phenotype Ontology, MP_0001135)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001135
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11 gene mutations causing the abnormal uterine cervix morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANTXR2 anthrax toxin receptor 2
BRCA1 breast cancer 1, early onset
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FANCL Fanconi anemia, complementation group L
HOXA13 homeobox A13
KISS1R KISS1 receptor
LHFPL2 lipoma HMGIC fusion partner-like 2
LOXL1 lysyl oxidase-like 1
OVOL1 ovo-like zinc finger 1
PAX8 paired box 8
TP63 tumor protein p63