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

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Gene: Scnn1a ENSRNOG00000019368

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Description

sodium channel epithelial 1 subunit alpha [Source:RGD Symbol;Acc:3639]

Location

Primary_assembly 4: 159,809,170-159,832,405 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant), 153 orthologues, 7 paralogues and is associated with 29 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000067271.3	Scnn1a-201	3120	699aa	ENSRNOP00000061813.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8QP47 Q6IRJ1	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,

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Summary

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