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

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Gene: SCNN1B ENSBTAG00000012290

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Description

sodium channel epithelial 1 subunit beta [Source:VGNC Symbol;Acc:VGNC:34356]

Location

Primary_assembly 25: 20,994,474-21,042,943 forward strand.

ARS-UCD2.0:CM008192.2

About this gene

This gene has 2 transcripts (splice variants), 151 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000016301.7	SCNN1B-201	2449	652aa	ENSBTAP00000016301.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6YXK2	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,
ENSBTAT00000091141.1	SCNN1B-202	2283	605aa	ENSBTAP00000096019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TD37	-

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Summary

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