Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Here, we review a proposed role for hemichannels in the pathogenesis of Keratitis-Ichthyosis-Deafness (KID) syndrome associated with connexin26 (Cx26) mutations. 21933663 2012
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Here, we assessed the effect of two Cx26 mutations associated with KID syndrome, Cx26I30N and D50Y, on protein biosynthesis and channel function in N2A and HeLa cells. 26831144 2016
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 CausalMutation disease CLINVAR GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review. 12172392 2002
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Germline missense mutations in GJB2, encoding connexin-26, were recently found to cause KID in 14 unrelated juvenile and adult patients. 15633193 2005
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Furthermore, we revealed that the expressions of IL15, CCL5, IL1A, IL23R and TLR5 are down-regulated in keratinocytes expressing Cx26-D50N, suggesting that immune deficiency in KID syndrome expressing Cx26-D50N might be associated not only with skin barrier defects, but also with the down-regulated expression of immune response-related genes. 30150638 2018
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 Biomarker disease BEFREE Excessive opening of undocked Cx26 hemichannels in the plasma membrane is associated with disease pathogenesis in keratitis-ichthyosis-deafness (KID) syndrome. 24939841 2014
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Dominant mutations in the Cx26 gene GJB2 have been shown to cause keratitis-ichthyosis-deafness (KID) syndrome, palmoplantar keratoderma associated with hearing loss, and Vohwinkel syndrome. 15140211 2004
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease UNIPROT De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome. 12548749 2003
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26. 19793313 2009
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 Biomarker disease GENOMICS_ENGLAND Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel. 31160754 2019
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 CausalMutation disease CLINVAR Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. 9285800 1997
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Collectively, these data provide insight into Cx26 structure-function and the underlying bases for the phenotypes associated with KID syndrome patients carrying the D50N mutation. 23797419 2013
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Clinical examination and molecular genetic analysis for mutations in the GJB2 gene were performed in 3 patients with KID syndrome ages 5, 13, and 41 years. 15691545 2005
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE Clinical examination and molecular analysis of GJB2 were performed in a cohort of 14 patients with KID syndrome originating from 11 families. 17381453 2007
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 CausalMutation disease CLINVAR Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolates. 18294064 2007
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 CausalMutation disease CLINVAR Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. 10376574 1999
Entrez Id: 10804
Gene Symbol: GJB6
GJB6
0.320 Biomarker disease BEFREE Because in the human skin connexin 26 (Cx26) is co-expressed with other connexins, like Cx43 and Cx30, and as the KID syndrome is inherited as autosomal dominant condition, it is possible that KID mutations change the way Cx26 interacts with other co-expressed connexins. 25625422 2015
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 AlteredExpression disease BEFREE Because in the human skin connexin 26 (Cx26) is co-expressed with other connexins, like Cx43 and Cx30, and as the KID syndrome is inherited as autosomal dominant condition, it is possible that KID mutations change the way Cx26 interacts with other co-expressed connexins. 25625422 2015
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome? 18950394 2009
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 Biomarker disease GENOMICS_ENGLAND A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triad. 15337980 2004
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 CausalMutation disease CLINVAR A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort. 17666888 2007
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE A group of human mutations within the N-terminal (NT) domain of connexin 26 (Cx26) hemichannels produce aberrant channel activity, which gives rise to deafness and skin disorders, including keratitis-ichthyosis-deafness (KID) syndrome. 30530766 2019
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E. 18024254 2008
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 GeneticVariation disease BEFREE A G12R (p.Gly12Arg) is a GJB2 mutation reported in only two patients with KID syndrome to date. 22011219 2012
Entrez Id: 2706
Gene Symbol: GJB2
GJB2
1.000 Biomarker disease BEFREE A 14-year-old girl with ichthyosis and severe liver disease is compared to 35 reported cases of KID or Senter syndrome. 1951425 1991