Diastasis Recti Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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 https://www.disgenet.org/browser/0/1/0/C0221766
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Genes

19 genes associated with the disease Diastasis Recti in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
B3GLCT beta 3-glucosyltransferase
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
COLEC10 collectin sub-family member 10 (C-type lectin)
COLEC11 collectin sub-family member 11
ELMO2 engulfment and cell motility 2
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GPC3 glypican 3
GPC4 glypican 4
H3F3A H3 histone, family 3A
IGF2 insulin-like growth factor 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MTOR mechanistic target of rapamycin (serine/threonine kinase)
PORCN porcupine homolog (Drosophila)
PPP2R3C protein phosphatase 2, regulatory subunit B'', gamma
SHPK sedoheptulokinase
SPECC1L sperm antigen with calponin homology and coiled-coil domains 1-like