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_006005.3GENCODE 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
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ENST00000506588.1WFS1-005587No protein-
 
Retained intron
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ENST00000513395.1WFS1-006570No protein-
 
Retained intron
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