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Symbol
Name
ID
H2-Ab1
histocompatibility 2, class II antigen A, beta 1
MGI:103070
Phenotype annotations related to hematopoietic system
!Indicates phenotype varies with strain background.
Darker colors indicate more annotations
Human Phenotypes
Decreased circulating IgA level
Polyclonal elevation of IgM
Decreased circulating antibody level
Secretory IgA deficiency
Abnormality of blood and blood-forming tissues
Abnormal bleeding
Purpura
Bone marrow hypocellularity
Pancytopenia
Aplastic anemia
Abnormal erythrocyte enzyme concentration or activity
Abnormal hemoglobin
Reduced beta/alpha synthesis ratio
Persistence of hemoglobin F
Increased mean corpuscular volume
Erythroid hyperplasia
Reticulocytosis
Anemia
Hemolytic anemia
Chronic hemolytic anemia
Microangiopathic hemolytic anemia
Hypochromic anemia
Hypochromic microcytic anemia
Iron deficiency anemia
Microcytic anemia
Schistocytosis
Eosinophilia
Increased T cell count
Lymphopenia
Leukocytosis
Leukopenia
Abnormal lymphocyte morphology
Abnormal granulocyte morphology
Abnormal basophil morphology
Acute lymphoblastic leukemia
Ph-positive acute lymphoblastic leukemia
T-cell acute lymphoblastic leukemias
Acute myeloid leukemia
Chronic myelogenous leukemia
Myeloproliferative disorder
Arterial thrombosis
Thromboembolism
Venous thrombosis
Deep venous thrombosis
Mesenteric venous thrombosis
Superficial thrombophlebitis
Prolonged prothrombin time
Thrombocytopenia
Autoimmune thrombocytopenia
Thrombocytosis
Lymphoma
Elevated erythrocyte sedimentation rate
Abnormality of the spleen
Asplenia
Splenic infarction
Splenomegaly
Hepatosplenomegaly
Disease(s) Associated with HLA-DQB1
acute lymphoblastic leukemia
acute myeloid leukemia
antiphospholipid syndrome
aplastic anemia
autoimmune polyendocrine syndrome type 2
autoimmune thrombocytopenic purpura
Behcet's disease
beta thalassemia
chronic myeloid leukemia
common variable immunodeficiency
IgA glomerulonephritis
immunoglobulin alpha deficiency
mycosis fungoides
paroxysmal nocturnal hemoglobinuria
pre-eclampsia
primary sclerosing cholangitis
rheumatoid arthritis
sarcoidosis
sickle cell anemia
systemic lupus erythematosus
thrombotic thrombocytopenic purpura

Mouse Phenotypes
abnormal T cell differentiation
abnormal CD4-positive T cell differentiation
increased double-negative T cell number
hemolytic anemia
increased B cell number
decreased CD4-positive, CD25-positive, alpha-beta regulatory T cell number
decreased CD4-positive, alpha-beta T cell number
absent CD4-positive, alpha-beta T cells
increased CD4-positive, alpha-beta T cell number
decreased CD8-positive, alpha-beta T cell number
increased CD8-positive, alpha-beta T cell number
decreased regulatory T cell number
decreased single-positive T cell number
abnormal CD4-positive, alpha beta T cell morphology
abnormal CD4-positive, CD25-positive, alpha-beta regulatory T cell morphology
abnormal spleen morphology
abnormal spleen B cell follicle morphology
absent spleen germinal center
abnormal spleen marginal zone morphology
abnormal spleen periarteriolar lymphoid sheath morphology
abnormal lymphocyte physiology
abnormal B cell physiology
abnormal immunoglobulin level
decreased IgG1 level
decreased IgG level
decreased IgM level
increased IgM level
abnormal T cell physiology
abnormal CD4-positive, alpha-beta T cell physiology
abnormal T cell activation
abnormal macrophage antigen presentation
Availability Mouse Genotype
H2-Ab1b-tm1.1Jssh/H2-Ab1b-tm1.1Jssh
H2-Ab1b-tm1Doi/H2-Ab1b-tm1Doi
H2-Ab1b-tm1Gru/H2-Ab1b-tm1Gru
H2-Ab1b-tm1Gru/H2-Ab1b-tm1Gru
Tg(Ab1TL)1Gru/0
H2-Ab1b-tm1Wug/H2-Ab1b-tm1Wug
H2-Ab1bm12/H2-Ab1bm12 !
H2-Ab1g7-em1Ygch/H2-Ab1g7-em1Ygch
H2-Ab1b-tm1Wug/H2-Ab1b-tm1Wug
Cd19tm1(cre)Cgn/Cd19+  (conditional)
H2-Ab1b-tm1Koni/H2-Ab1b-tm1.1Koni
Tg(Tek-cre)12Flv/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
05/14/2024
MGI 6.23
The Jackson Laboratory