Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: scn2b ENSDARG00000101713

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Description

sodium channel, voltage-gated, type II, beta [Source:NCBI gene (formerly Entrezgene);Acc:777666]

Location

Chromosome 15: 12,521,379-12,545,683 reverse strand.

GRCz11:CM002899.2

About this gene

This gene has 3 transcripts (splice variants), 190 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000162807.2	scn2b-203	918	230aa	ENSDARP00000131257.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q06W28	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, 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,
ENSDART00000162601.2	scn2b-202	2448	223aa	ENSDARP00000138751.1	Nonsense mediated decay	-	-
ENSDART00000161274.2	scn2b-201	820	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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