EMBL-EBI User Survey 2024

Do data resources managed by EMBL-EBI and our collaborators make a difference to your work?

Please take 10 minutes to fill in our annual user survey, and help us make the case for why sustaining open data resources is critical for life sciences research.

Survey link: https://www.surveymonkey.com/r/HJKYKTT?channel=[webpage]

Human (GRCh37.p13)
Description

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

Gene Synonyms

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

Location

Chromosome 4: 6,271,576-6,304,992 forward strand.

GRCh37:CM000666.1

About this gene

This gene has 6 transcripts (splice variants) and is associated with 14 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000226760.1WFS1-0013640890aaENSP00000226760.1
 
Protein coding
CCDS3386B4DJ99 O76024 NM_006005.3Ensembl CanonicalGENCODE 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
---