Symbol Name ID |
Slc4a2
solute carrier family 4 (anion exchanger), member 2 MGI:109351 |
Darker colors indicate more annotations |
Human Phenotypes | Bruising susceptibility |
Anemia |
Splenomegaly |
Disease(s) Associated with SLC4A2 | |||
osteopetrosis |
Mouse Phenotypes | abnormal osteoclast morphology |
abnormal osteoclast physiology |
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Availability | Mouse Genotype | ||
Slc4a2tm1Ges/Slc4a2tm1Ges | |||
Slc4a2tm2Ges/Slc4a2tm2Ges Ctsktm1(cre)Ska/Ctsk+ (conditional) |
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Slc4a2tm2Ges/Slc4a2tm2Ges Tg(Mx1-cre)1Cgn/0 (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 04/30/2024 MGI 6.23 |
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