2024年12月25日 · GJB6 (Gap Junction Protein Beta 6) is a Protein Coding gene. Diseases associated with GJB6 include Clouston Syndrome and Deafness, Autosomal Recessive 1B. …

Gap junction beta-6 protein (GJB6), also known as connexin 30 (Cx30) — is a protein that in humans is encoded by the GJB6 gene. [5] [6] [7] Connexin 30 (Cx30) is one of several gap …

The GJB6 gene provides instructions for making a protein called gap junction beta 6, more commonly known as connexin 30. Connexin 30 is a member of the connexin protein family. …

This study aimed to investigate GJB2 (connexin 26) and GJB6 (connexin 30) mutations associated with familial non-syndromic childhood hearing impairment (HI) in Cameroon. We …

Connexin-30 (GJB6) is a gap junction subunit expressed abundantly in brain and cochlea (summary by Dahl et al., 1996; Lautermann et al., 1998). Dahl et al. (1996) cloned a cDNA of …

2025年1月4日 · gap junction beta-6 protein, connexin 30, ectodermal dysplasia 2, hidrotic (Clouston syndrome), gap junction protein, beta 6, 30kDa. GeneRIFs: Gene References Into …

GJB6 is a prognostic marker in Pancreatic adenocarcinoma Cancer specificity i Specificity of RNA expression in 17 cancer types is categorized as either cancer enriched, group enriched, …

2014年1月30日 · Clinical resource with information about GJB6, Autosomal dominant nonsyndromic hearing loss 3B, Autosomal recessive nonsyndromic hearing loss 1A, …

This gene has 14 transcripts (splice variants), 284 orthologues, 20 paralogues and is associated with 12 phenotypes. Biased expression in esophagus (RPKM 49.4), bone marrow (RPKM …

The GJB2 and GJB6 genes on human chromosome 13q12 and common recessive mutations associated with nonsyndromic recessive deafness. Shown is a map of the region of …