Gene: CDKN1C ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1028
Gene Symbol: CDKN1C
CDKN1C 		0.030 Biomarker disease BEFREE CDKN1C sequencing should be performed for BWS patients presenting with abdominal wall defects or cleft palate without 11p15 methylation defects or body asymmetry, or in familial cases of BWS. 26077438 2015
Entrez Id: 1028
Gene Symbol: CDKN1C
CDKN1C 		0.030 GeneticVariation disease BEFREE A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases. 23197429 2013
Entrez Id: 1028
Gene Symbol: CDKN1C
CDKN1C 		0.030 GeneticVariation disease BEFREE Polydactyly, genital abnormalities, extra nipple, and cleft palate are more frequently observed in BWS with mutations in CDKN1C. 20503313 2010