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Symbol
Name
ID
Wfs1
wolframin ER transmembrane glycoprotein
MGI:1328355
Phenotype annotations related to endocrine/exocrine glands
Darker colors indicate more annotations
Human Phenotypes
Diabetes mellitus
Type II diabetes mellitus
Hypothyroidism
Diabetes insipidus
Delayed puberty
Hypogonadism
Male hypogonadism
Disease(s) Associated with WFS1
autosomal dominant Wolfram syndrome
optic atrophy
type 1 diabetes mellitus
type 2 diabetes mellitus
Wolfram syndrome
Wolfram syndrome 1

Mouse Phenotypes
abnormal pancreatic islet morphology
decreased pancreatic beta cell mass
decreased pancreatic beta cell number
disorganized pancreatic islets
abnormal thyroid gland morphology
abnormal thyroid follicle morphology
abnormal seminiferous tubule morphology
abnormal seminiferous tubule epithelium morphology
decreased Sertoli cell number
increased glucagon secretion
abnormal pancreatic beta cell physiology
decreased insulin secretion
abnormal pancreas secretion
Availability Mouse Genotype
Wfs1tm1Koks/Wfs1tm1Koks
Wfs1tm1Yoka/Wfs1tm1Yoka
Wfs1tm1Perm/Wfs1tm1Perm
Tg(Ins2-cre)23Herr/0  (conditional)

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
04/30/2024
MGI 6.23
The Jackson Laboratory