Symbol Name ID |
Stx16
syntaxin 16 MGI:1923396 |
Darker colors indicate more annotations |
Human Phenotypes | Enamel hypoplasia |
Short neck |
Diaphyseal sclerosis |
Brachydactyly |
Cortical subperiosteal resorption of humeral metaphyses |
Short metacarpal |
Increased bone mineral density |
Increased bone density with cystic changes |
Disease(s) Associated with STX16 | ||||||||
pseudohypoparathyroidism type IB |
Mouse Phenotypes | increased bone mineral content |
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Availability | Mouse Genotype | |
Stx16tm1b(KOMP)Wtsi/Stx16tm1b(KOMP)Wtsi |
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 09/03/2024 MGI 6.24 |
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