diastasis recti Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A separation of the rectus abdominis muscle into right and left halves (which are normally joined at the midline at the linea alba). (Human Phenotype Ontology, HP_0001540)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001540
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Genes

11 genes associated with the diastasis recti phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
COLEC11 collectin sub-family member 11
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GPC3 glypican 3
H19 H19, imprinted maternally expressed transcript (non-protein coding)
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
NSD1 nuclear receptor binding SET domain protein 1
PORCN porcupine homolog (Drosophila)