Description

sodium channel, voltage gated, type X alpha subunit [Source:HGNC Symbol;Acc:HGNC:10582]

Synonyms

hPN3, Nav1.8, PN3, SNS

Location
INSDC coordinates

chromosome:GRCh38:CM000665.2:38696802:38794010:1

About this gene

This gene has 1 transcript (splice variant), 73 orthologues, 19 paralogues, is a member of 1 Ensembl protein family and is associated with 5 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SCN10A-001ENST0000044908264181956aaENSP00000390600
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS33736Q9Y5Y9 NM_001293306
NM_006514
NP_001280235
NP_006505
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.

Genomic alignments
Gene tree
Orthologues
Paralogues
Families

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

Gene-based displays