uterus hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001121
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13 gene mutations causing the uterus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CENPB centromere protein B, 80kDa
CGA glycoprotein hormones, alpha polypeptide
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
ESR1 estrogen receptor 1
FANCC Fanconi anemia, complementation group C
GNRHR gonadotropin-releasing hormone receptor
KISS1R KISS1 receptor
LBR lamin B receptor
LHB luteinizing hormone beta polypeptide
LMX1A LIM homeobox transcription factor 1, alpha
PAX8 paired box 8
SGPL1 sphingosine-1-phosphate lyase 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor