Gene: Wfs1 (Wolfram syndrome 1 (wolframin)) Rattus norvegicus
Symbol: Wfs1
Name: Wolfram syndrome 1 (wolframin)
Description: ENCODES a protein that exhibits calcium-dependent protein binding; calmodulin binding; activating transcription factor binding (ortholog); INVOLVED IN olfactory behavior; pancreas development; calcium ion homeostasis (ortholog); PARTICIPATES IN Endoplasmic Reticulum-associated degradation pathway; ASSOCIATED WITH Seizures; Stress Disorders, Post-Traumatic; Cataract, Nuclear Total (ortholog); FOUND IN endoplasmic reticulum (ortholog); integral component of endoplasmic reticulum membrane (ortholog); INTERACTS WITH ammonium chloride; Decabromodiphenyl oxide; dibutyl phthalate
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: Wolfram syndrome 1; Wolfram syndrome 1 homolog; Wolfram syndrome 1 homolog (human); wolframin
Orthologs:
Latest Assembly: RGSC Genome Assembly v5.0
Position:
MapChrPositionStrandSource
RGSC Genome Assembly v6.01478,640,707 - 78,665,224+NCBI
Rat Cytogenetic Map14q21 NCBI
RGSC Genome Assembly v5.01478,606,172 - 78,630,689+NCBI
RGSC Genome Assembly v3.41479,379,680 - 79,404,003+NCBI
Rat Celera Assembly1472,756,725 - 72,781,236+NCBI
Genome Assembly 3.11479,389,637 - 79,406,394+NCBI
Model

Launch Genome Browser (GBrowse)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
QTLs in Region (RGSC Genome Assembly v5.0)

Sequence

Nucleotide Sequences
Protein Sequences

Strain Variation

Strain Sequence Variants

Additional Information

External Database Links
Nomenclature History
RGD Curation Notes
 
More on Wfs1
Entrez Gene
Ensembl Gene
Genome Browser
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 68954
Created: 2001-11-06
Species: Rattus norvegicus
Last Modified: 2014-11-11
Status: ACTIVE