Symbol Name ID |
Snx10
sorting nexin 10 MGI:1919232 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Disease(s) Associated with SNX10 | |
autosomal recessive osteopetrosis 8 |
Mouse Phenotypes | decreased osteoclast cell number |
abnormal osteoclast morphology |
abnormal osteoclast physiology |
osteomyelitis |
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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) |
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 05/28/2024 MGI 6.13 |
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