Symbol Name ID |
Wfs1
wolframin ER transmembrane glycoprotein MGI:1328355 |
Darker colors indicate more annotations |
Human Phenotypes | Diabetes mellitus |
Hypothyroidism |
Diabetes insipidus |
Delayed puberty |
Hypogonadism |
Male hypogonadism |
Disease(s) Associated with WFS1 | ||||||
optic atrophy | ||||||
Wolfram syndrome |
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) |
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 06/12/2024 MGI 6.13 |
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