bicornuate uterus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a bicornuate uterus. (Human Phenotype Ontology, HP_0000813)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000813
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Genes

16 genes associated with the bicornuate uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DHCR7 7-dehydrocholesterol reductase
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
HNF1B HNF1 homeobox B
ITGA8 integrin, alpha 8
LRP2 low density lipoprotein receptor-related protein 2
MNX1 motor neuron and pancreas homeobox 1
PAX2 paired box 2
RARB retinoic acid receptor, beta
RET ret proto-oncogene
SETBP1 SET binding protein 1
SF3B4 splicing factor 3b, subunit 4, 49kDa
STRA6 stimulated by retinoic acid 6
TNXB tenascin XB