Human (GRCh37.p13)
Description

Wolfram syndrome 1 (wolframin) [Source:HGNC Symbol;Acc:12762]

Gene Synonyms

DFNA14, DFNA38, DFNA6, DIDMOAD, WFRS, WFS, WFSL

Location
About this transcript

This transcript has 8 exons, is annotated with 41 domains and features, is associated with 20976 variant alleles and maps to 450 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000226760.1WFS1-0013640890aaENSP00000226760.1
 
Protein coding
CCDS3386B4DJ99 O76024 NM_006005.3GENCODE basic
ENST00000503569.1WFS1-0083255890aaENSP00000423337.1
 
Protein coding
CCDS3386B4DJ99 O76024 -GENCODE basic
ENST00000506362.1WFS1-007755252aaENSP00000424103.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000507765.1WFS1-0043655No protein-
 
Retained intron
---
ENST00000506588.1WFS1-005587No protein-
 
Retained intron
---
ENST00000513395.1WFS1-006570No protein-
 
Retained intron
---
Statistics

Exons: 8, Coding exons: 7, Transcript length: 3,640 bps, Translation length: 890 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O76024

CCDS

This transcript is a member of the Human CCDS set: CCDS3386

Version

ENST00000226760.1

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000206863 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.