Description

gap junction protein, beta 3, 31kDa [Source:HGNC Symbol;Acc:HGNC:4285]

Synonyms

CX31, DFNA2, EKV

Location
INSDC coordinates

chromosome:GRCh38:CM000663.2:34781189:34786369:1

About this gene

This gene has 2 transcripts (splice variants), 63 orthologues, 8 paralogues, is a member of 1 Ensembl protein family and is associated with 11 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
GJB3-002ENST000003733662217270aaENSP00000362464
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS384O75712 NM_024009
NP_076872
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

GJB3-001ENST000003733621797270aaENSP00000362460
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS384O75712 NM_001005752
NP_001005752
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays