Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 GeneticVariation disease BEFREE Here we describe 33 patients with PYCR1-related ARCL from 27 families with initial diagnoses varying between wrinkly skin syndrome, gerodermia osteodysplastica, De Barsy syndrome or more severe progeria syndromes. 24035636 2013
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 Biomarker disease GENOMICS_ENGLAND Mutations in the ATP6V0A2 gene were found to underlie both, autosomal recessive cutis laxa type 2 (ARCL2), Debré type, and wrinkly skin syndrome (WSS). 22773132 2012
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 GeneticVariation disease BEFREE Mutations in the ATP6V0A2 gene were found to underlie both, autosomal recessive cutis laxa type 2 (ARCL2), Debré type, and wrinkly skin syndrome (WSS). 22773132 2012
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 Biomarker disease CTD_human We identified loss-of-function mutations in ATP6V0A2, encoding the a2 subunit of the V-type H+ ATPase, in several families with autosomal recessive cutis laxa type II or wrinkly skin syndrome. 18157129 2008
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 GermlineCausalMutation disease ORPHANET We identified loss-of-function mutations in ATP6V0A2, encoding the a2 subunit of the V-type H+ ATPase, in several families with autosomal recessive cutis laxa type II or wrinkly skin syndrome. 18157129 2008
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 GeneticVariation disease BEFREE Importantly, our study demonstrates that GO is not allelic to wrinkly skin syndrome caused by mutations in ATP6V0A2. 19006212 2008
Entrez Id: 23545
Gene Symbol: ATP6V0A2
ATP6V0A2
0.730 CausalMutation disease CLINVAR
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 GeneticVariation disease BEFREE This report describes two unrelated Portuguese patients, age 11 and 17 years, with a phenotype concordant with WSS and clinical and molecular diagnosis of WSS by the identification of two novel frameshift variants in the KMT2A gene. 31710778 2020
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 GeneticVariation disease BEFREE We diagnosed a Chinese boy who presented postnatal growth retardation with WSS caused by a novel de novo mutation in KMT2A. 31250358 2019
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 PosttranslationalModification disease BEFREE As KMT2A is known to regulate the expression of multiple target genes through methylation of lysine 4 of histone 3 (H3K4me), we sought to investigate the transcriptomic consequences of KMT2A variants involved in WSS. 30014449 2018
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 Biomarker disease BEFREE Following the identification of the causative gene (KMT2A) in 2012, only 31 cases of WSS have been described precisely in the literature. 29574747 2018
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 GeneticVariation disease BEFREE WSS is caused by heterozygous mutations in KMT2A (also known as MLL), a gene encoding a histone methyltransferase. 25810209 2016
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 GeneticVariation disease BEFREE This report expands the phenotypic spectrum of the clinical phenotypes and KMT2A variants associated with WSS. 24886118 2014
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A
0.360 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17
0.030 GeneticVariation disease BEFREE Nine C2orf37 mutations causing WSS have been identified. 24015686 2014
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17
0.030 GeneticVariation disease BEFREE A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani origin. 21963443 2011
Entrez Id: 80067
Gene Symbol: DCAF17
DCAF17
0.030 GeneticVariation disease BEFREE This study doubles the number of known mutations for this disorder, confirms that truncating mutations in C2orf37 are the only known cause of WSS, and suggests that mutations in this gene do not contribute significantly to cases presenting with isolated elements of WSS such as deafness and dystonia. 20507343 2010