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Symbol
Name
ID
H2-Ab1
histocompatibility 2, class II antigen A, beta 1
MGI:103070
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Decreased circulating IgA level
Polyclonal elevation of IgM
Decreased circulating antibody level
Secretory IgA deficiency
Abnormal erythrocyte enzyme concentration or activity
Abnormality of metabolism/homeostasis
Hypercalcemia
Hyperkalemia
Hyponatremia
Abnormality of iron homeostasis
Decreased circulating iron concentration
Decreased level of 1,5 anhydroglucitol in serum
Unconjugated hyperbilirubinemia
Increased blood urea nitrogen
Elevated circulating creatinine concentration
Hypoalbuminemia
Elevated circulating C-reactive protein concentration
Reduced haptoglobin level
Increased CSF protein concentration
Elevated circulating hepatic transaminase concentration
Increased circulating lactate dehydrogenase concentration
Elevated alkaline phosphatase of hepatic origin
Reduced leukocyte alkaline phosphatase
Elevated erythrocyte sedimentation rate
Hyperglycemia
Hypoglycemia
Diabetes mellitus
Type I diabetes mellitus
Type II diabetes mellitus
Increased circulating lactate concentration
Ketoacidosis
Renal Fanconi syndrome
Edema
Joint swelling
Pleural effusion
Chylothorax
Pulmonary edema
Abnormality of temperature regulation
Fever
Hypothermia
Reduced circulating vitamin A concentration
Decreased circulating vitamin E concentration
Decreased circulating vitamin D concentration
Decreased circulating vitamin K concentration
Hypercalciuria
Hematuria
Microscopic hematuria
Pyuria
Glycosuria
Decreased level of D-mannose in urine
Proteinuria
Hemoglobinuria
Paroxysmal nocturnal hemoglobinuria
Hemosiderinuria
Ascites
Increased circulating free T3
Increased circulating free T4 concentration
Decreased thyroid-stimulating hormone level
Atypical scarring of skin
Scarring
Disease(s) Associated with HLA-DQB1
Addison's disease
autoimmune polyendocrine syndrome type 2
Behcet's disease
beta thalassemia
chronic myeloid leukemia
common variable immunodeficiency
Creutzfeldt-Jakob disease
Graves' disease
IgA glomerulonephritis
immunoglobulin alpha deficiency
narcolepsy
paroxysmal nocturnal hemoglobinuria
pemphigus vulgaris
pre-eclampsia
primary sclerosing cholangitis
rheumatoid arthritis
sarcoidosis
sickle cell anemia
Sjogren's syndrome
systemic lupus erythematosus
thrombotic thrombocytopenic purpura
type 1 diabetes mellitus

Mouse Phenotypes
increased urine protein level
abnormal response/metabolism to endogenous compounds
Availability Mouse Genotype
H2-Ab1bm12/H2-Ab1bm12

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
05/14/2024
MGI 6.23
The Jackson Laboratory