abnormal uterus weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the weight of the female organ of gestation (Mammalian Phenotype Ontology, MP_0004903)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004903
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Genes

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

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CBS cystathionine-beta-synthase
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CHST10 carbohydrate sulfotransferase 10
CHST8 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DFNB31 deafness, autosomal recessive 31
EGR1 early growth response 1
EPHA1 EPH receptor A1
ERRFI1 ERBB receptor feedback inhibitor 1
ESR1 estrogen receptor 1
FSHR follicle stimulating hormone receptor
GHR growth hormone receptor
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LEPR leptin receptor
LHX3 LIM homeobox 3
MARK2 MAP/microtubule affinity-regulating kinase 2
NR5A2 nuclear receptor subfamily 5, group A, member 2
PHB2 prohibitin 2
TIMP1 TIMP metallopeptidase inhibitor 1
UBE3A ubiquitin protein ligase E3A
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
VGF VGF nerve growth factor inducible