Description

SRY (sex determining region Y)-box 2 [Source:HGNC Symbol;Acc:HGNC:11195]

INSDC coordinates

chromosome:GRCh38:CM000665.2:181711924:181714436:1

About this gene

This gene has 1 transcript (splice variant), 44 orthologues, 16 paralogues, is a member of 1 Ensembl protein family and is associated with 7 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SOX2-001ENST000003254042513317aaENSP00000323588
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS3239P48431 NM_003106
NP_003097
TSL:NA

Transcript Support Level Not Analysed. Pseudogenes, single exon transcripts, HLA, T-cell receptor and Ig transcripts are not analysed and therefore not given any of the TSL categories.

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.

Gene-based displays