decreased uterus weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the weight of the female organ of gestation (Mammalian Phenotype Ontology, MP_0004905)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004905
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Genes

15 gene mutations causing the decreased uterus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DFNB31 deafness, autosomal recessive 31
EGR1 early growth response 1
ESR1 estrogen receptor 1
FSHR follicle stimulating hormone receptor
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LEPR leptin receptor
LHX3 LIM homeobox 3
MARK2 MAP/microtubule affinity-regulating kinase 2
UBE3A ubiquitin protein ligase E3A
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
VGF VGF nerve growth factor inducible