Symbol Name ID |
Slc4a2
solute carrier family 4 (anion exchanger), member 2 MGI:109351 |
Darker colors indicate more annotations |
Human Phenotypes | Craniosynostosis |
Macrocephaly |
Bowing of the long bones |
Abnormal metaphysis morphology |
Bone pain |
Recurrent fractures |
Abnormal epiphysis morphology |
Abnormal rib morphology |
Narrow chest |
Osteopetrosis |
Reduced bone mineral density |
Disease(s) Associated with SLC4A2 | |||||||||||
osteopetrosis |
Mouse Phenotypes | failure of tooth eruption |
abnormal osteoclast morphology |
abnormal osteoclast physiology |
abnormal long bone morphology |
abnormal long bone metaphysis morphology |
abnormal bone marrow cavity morphology |
increased trabecular bone volume |
abnormal trabecular bone morphology |
increased bone trabecula number |
increased trabecular bone thickness |
increased bone mass |
osteopetrosis |
abnormal skeleton development |
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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 05/14/2024 MGI 6.23 |
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