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 20683 variant alleles and maps to 476 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: 3,255 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

ENST00000503569.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000358733 (version 1)
GENCODE basic gene

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