Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 GeneticVariation disease BEFREE We did not find evidence for interaction between maternal pre-pregnancy obesity and variants in MKKS, a gene previously associated with obesity, on the risk of anorectal atresia. 23127126 2013
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 GeneticVariation disease BEFREE Our results suggest that genetic variation in the MKKS gene may play a role in the development of obesity and the metabolic syndrome. 18813213 2008
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 Biomarker disease BEFREE Variants in BBS2, BBS4, and BBS6 showed evidence of association with common obesity in an age-dependent manner, the BBS2 single nucleotide polymorphism (SNP) being associated with common adult obesity (P = 0.0005) and the BBS4 and BBS6 SNPs being associated with common early-onset childhood obesity (P = 0.0003) and common adult morbid obesity (0.0003 < P < 0.007). 17003356 2006
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 GeneticVariation disease BEFREE Mutations in the MKKS gene have also been shown to cause some cases of Bardet-Biedl syndrome (BBS) which is characterized by obesity, pigmentary retinopathy, polydactyly, renal abnormalities and hypogenitalism with secondary features of hypertension and diabetes. 15772095 2005
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 Biomarker disease BEFREE Obesity is a prominent feature of the Bardet-Biedl syndrome (BBS), one subset of which, BBS6, is due to mutations in the chaperonin-like gene termed the McKusick-Kaufman syndrome (MKKS) gene. 15483080 2005
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 Biomarker disease MGD Mutations in the MKKS gene have also been shown to cause some cases of Bardet-Biedl syndrome (BBS) which is characterized by obesity, pigmentary retinopathy, polydactyly, renal abnormalities and hypogenitalism with secondary features of hypertension and diabetes. 15772095 2005
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 GeneticVariation disease BEFREE Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome. 10973251 2000
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 Biomarker disease HPO
Entrez Id: 8195
Gene Symbol: MKKS
MKKS
0.660 Biomarker disease GENOMICS_ENGLAND