Symbol Name ID |
Slc10a7
solute carrier family 10 (sodium/bile acid cotransporter family), member 7 MGI:1924025 |
Reference
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J:265027 Dubail J, Huber C, Chantepie S, Sonntag S, Tuysuz B, Mihci E, Gordon CT, Steichen-Gersdorf E, Amiel J, Nur B, Stolte-Dijkstra I, van Eerde AM, van Gassen KL, Breugem CC, Stegmann A, Lekszas C, Maroofian R, Karimiani EG, Bruneel A, Seta N, Munnich A, Papy-Garcia D, De La Dure-Molla M, Cormier-Daire V, SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects. Nat Commun. 2018 Aug 6;9(1):3087 |
Age | E12.5 | E14.5 | E16.5 | P |
Immunohistochemistry (section) | ||||
In situ RNA (section) | ||||
Immunohistochemistry (whole mount) | ||||
In situ RNA (whole mount) | ||||
In situ reporter (knock in) | ||||
Northern blot | ||||
Western blot | ||||
RT-PCR | ||||
cDNA clones | ||||
RNase protection | ||||
Nuclease S1 | ||||
Primer Extension |
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 12/10/2024 MGI 6.24 |
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