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Symbol
Name
ID
Wfs1
wolframin ER transmembrane glycoprotein
MGI:1328355
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Feeding difficulties in infancy
Depression
Atypical behavior
Autism
Polydipsia
Polyphagia
Fatigue
Myalgia
Disease(s) Associated with WFS1
autosomal dominant Wolfram syndrome
optic atrophy
type 1 diabetes mellitus
Wolfram syndrome
Wolfram syndrome 1

Mouse Phenotypes
behavior/neurological phenotype
abnormal behavioral response to addictive substance
impaired behavioral response to addictive substance
abnormal associative learning
enhanced active avoidance behavior
enhanced passive avoidance behavior
abnormal cued conditioning behavior
decreased exploration in new environment
abnormal spatial learning
abnormal eating behavior
decreased food intake
increased coping response
increased anxiety-related response
increased thigmotaxis
abnormal postural reflex
impaired righting response
impaired coordination
impaired swimming
head bobbing
decreased vertical activity
increased vertical activity
decreased locomotor activity
increased locomotor activity
circling
analgesia
decreased copulatory plug deposition
abnormal social investigation
abnormal vocalization
Availability Mouse Genotype
Wfs1tm1.1Bedel/Wfs1tm1.1Bedel
Wfs1tm1Koks/Wfs1tm1Koks *
Wfs1tm1Yoka/Wfs1tm1Yoka
Wfs1tm1Koks/Wfs1+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory