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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
H2-K1
histocompatibility 2, K1, K region
MGI:95904
20 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
H2-K1b-tm1Bpe/H2-K1b-tm1Bpe
involves: 129P2/OlaHsd * C57BL/6
decreased CD8-positive, alpha-beta T cell number J:54709
increased CD4-positive, alpha-beta T cell number J:54709
H2-K1d-em4Dvs/H2-K1d-em4Dvs
NOD/ShiLtDvs-H2-K1d-em4Dvs/Dvs
abnormal immune system physiology J:257229
decreased susceptibility to autoimmune diabetes J:257229
H2-K1d-em5Dvs/H2-K1d-em5Dvs
NOD/ShiLtDvs-H2-K1d-em5Dvs/Dvs
abnormal immune system physiology J:257229
decreased susceptibility to autoimmune diabetes J:257229
H2-K1d-em7Dvs/H2-K1d-em7Dvs
NOD/ShiLtDvs-H2-K1d-em7Dvs/Dvs
abnormal immune system physiology J:257229
decreased susceptibility to autoimmune diabetes J:257229
Tg(CKMM-tTA)A3Rhvh/0
Tg(tetO-H2-K1)#Papl/0
B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl
abnormal circulating enzyme level J:205907
abnormal cytokine level J:205907
abnormal skeletal muscle morphology J:205907
abnormal spine curvature J:205907
cachexia J:205907
decreased body weight J:205907
decreased locomotor activity J:205907
increased anti-nuclear antigen antibody level J:205907
increased autoantibody level J:205907
increased circulating creatine kinase level J:205907
normal mortality/aging J:205907
muscle weakness J:205907
myositis J:205907
perinatal lethality, complete penetrance J:205907
skeletal muscle fiber atrophy J:205907
skeletal muscle fiber degeneration J:205907

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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
11/19/2024
MGI 6.24
The Jackson Laboratory