Symbol Name ID |
Ptpn22
protein tyrosine phosphatase, non-receptor type 22 (lymphoid) MGI:107170 |
Darker colors indicate more annotations |
Human Phenotypes | Hematuria |
Pyuria |
Decreased level of D-mannose in urine |
Proteinuria |
Abnormality of the kidney |
Lupus nephritis |
Tubulointerstitial nephritis |
Abnormal renal physiology |
Polyuria |
Nephritis |
Renal insufficiency |
Disease(s) Associated with PTPN22 | |||||||||||
Behcet's disease | |||||||||||
Sjogren's syndrome | |||||||||||
systemic lupus erythematosus | |||||||||||
temporal arteritis | |||||||||||
type 1 diabetes mellitus |
Mouse Phenotypes | glomerulonephritis |
expanded mesangial matrix |
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Availability | Mouse Genotype | ||
Ptpn22tm1.1Draw/Ptpn22tm1.1Draw | |||
Gt(ROSA)26Sortm1(Ptpn22*)Draw/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+ (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 08/02/2024 MGI 6.24 |
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