Gene: SCN2B ENSG00000149575

Description

sodium voltage-gated channel beta subunit 2 [Source:HGNC Symbol;Acc:HGNC:10589]

Location

Chromosome 11: 118,162,806-118,176,639 reverse strand.

GRCh38:CM000673.2

About this gene

This gene has 4 transcripts (splice variants), 189 orthologues, 6 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000278947.6	SCN2B-201	4937	215aa	ENSP00000278947.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS8390	O60939 Q5U0K8	NM_004588.5	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1, TSL 1: A transcript where all splice junctions 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, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENST00000658882.1	SCN2B-202	1207	92aa	ENSP00000499572.1	Nonsense mediated decay		A0A590UJS3	-	-
ENST00000669850.1	SCN2B-204	1238	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	-
ENST00000665446.1	SCN2B-203	601	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	-

Gene: SCN2B ENSG00000149575

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Gene: SCN2B ENSG00000149575

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