abnormal uterine cervix size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the size of the lower opening of the uterus to the vagina (Mammalian Phenotype Ontology, MP_0009225)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009225
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3 gene mutations causing the abnormal uterine cervix size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FANCL Fanconi anemia, complementation group L
HOXA13 homeobox A13
KISS1R KISS1 receptor