Description

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

Synonyms

DFNA14, DFNA38, DFNA6, DIDMOAD, WFS

Location
About this transcript

This transcript has 8 exons, is annotated with 41 domains and features, is associated with 837 variations and maps to 26 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
WFS1-001ENST000002267603640890aaENSP00000226760
 
Protein coding
CCDS3386O76024 NM_001145853
NM_006005
NP_001139325
NP_005996
TSL:1GENCODE basicAPPRIS P2
WFS1-008ENST000005035693255890aaENSP00000423337
 
Protein coding
CCDS3386O76024 -TSL:1GENCODE basicAPPRIS P2
WFS1-007ENST00000506362755252aaENSP00000424103
 
Protein coding
-H0Y9G5 -CDS 5' and 3' incompleteTSL:3APPRIS ALT2
WFS1-004ENST000005077653655No protein-
 
Retained intron
---TSL:2
WFS1-005ENST00000506588587No protein-
 
Retained intron
---TSL:2
WFS1-006ENST00000513395570No protein-
 
Retained intron
---TSL:2
Statistics

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

CCDS

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

Uniprot

This transcript corresponds to the following Uniprot identifiers: O76024

Transcript Support Level (TSL)

TSL:1

Ensembl version

ENST00000226760.5

Type

Known protein coding

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
GENCODE basic gene

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

Transcript-based displays