Symbol Name ID |
H2-Ab1
histocompatibility 2, class II antigen A, beta 1 MGI:103070 |
Darker colors indicate more annotations |
Human Phenotypes | Renal Fanconi syndrome |
Hypercalciuria |
Hematuria |
Microscopic hematuria |
Pyuria |
Glycosuria |
Decreased level of D-mannose in urine |
Proteinuria |
Hemoglobinuria |
Paroxysmal nocturnal hemoglobinuria |
Hemosiderinuria |
Nocturia |
Abnormality of the kidney |
IgA deposition in the glomerulus |
Lupus nephritis |
Tubulointerstitial nephritis |
Nephrocalcinosis |
Nephrolithiasis |
Abnormal renal physiology |
Polyuria |
Hemolytic-uremic syndrome |
Nephritis |
Renal insufficiency |
Acute kidney injury |
Chronic kidney disease |
Stage 5 chronic kidney disease |
Renal cell carcinoma |
Disease(s) Associated with HLA-DQB1 | |||||||||||||||||||||||||||
Behcet's disease | |||||||||||||||||||||||||||
colorectal cancer | |||||||||||||||||||||||||||
IgA glomerulonephritis | |||||||||||||||||||||||||||
narcolepsy | |||||||||||||||||||||||||||
paroxysmal nocturnal hemoglobinuria | |||||||||||||||||||||||||||
pre-eclampsia | |||||||||||||||||||||||||||
primary sclerosing cholangitis | |||||||||||||||||||||||||||
sarcoidosis | |||||||||||||||||||||||||||
sickle cell anemia | |||||||||||||||||||||||||||
Sjogren's syndrome | |||||||||||||||||||||||||||
systemic lupus erythematosus | |||||||||||||||||||||||||||
thrombotic thrombocytopenic purpura | |||||||||||||||||||||||||||
type 1 diabetes mellitus |
Mouse Phenotypes | increased urine protein level |
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Availability | Mouse Genotype | |
H2-Ab1bm12/H2-Ab1bm12 |
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 |
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