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Symbol Name ID |
Snx10
sorting nexin 10 MGI:1919232 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Macrocephaly |
Osteopetrosis |
| Disease(s) Associated with SNX10 | |||
| autosomal recessive osteopetrosis 8 |
| Mouse Phenotypes | failure of tooth eruption |
tooth impaction |
absent teeth |
decreased osteoclast cell number |
abnormal osteoclast morphology |
abnormal osteoclast physiology |
osteomyelitis |
abnormal femur morphology |
decreased femur compact bone thickness |
abnormal long bone metaphysis morphology |
abnormal bone structure |
decreased bone mineral content |
decreased bone mineral density of femur |
decreased bone mineral density |
increased bone mineral density |
decreased bone volume |
increased bone volume |
decreased compact bone thickness |
decreased osteoblast cell number |
abnormal trabecular bone morphology |
increased bone trabecula number |
decreased bone trabecular spacing |
increased trabecular bone thickness |
osteopetrosis |
abnormal skeleton development |
abnormal epiphyseal plate morphology |
increased osteoid volume |
osteomalacia |
rickets |
decreased bone resorption |
decreased bone stiffness |
decreased bone strength |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||||||||
| Snx10em1Ael/Snx10em1Ael | |||||||||||||||||||||||||||||||||
| Snx10em2Ael/Snx10em2Ael | |||||||||||||||||||||||||||||||||
| Snx10tm1a(EUCOMM)Raba/Snx10tm1a(EUCOMM)Raba | |||||||||||||||||||||||||||||||||
| Ctsktm1(cre)Ska/Ctsk+ Snx10tm1c(EUCOMM)Raba/Snx10tm1c(EUCOMM)Raba (conditional) |
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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 04/16/2024 MGI 6.23 |
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