Gene Expression Literature Detail
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Symbol Name ID |
Slc10a7
solute carrier family 10 (sodium/bile acid cotransporter family), member 7 MGI:1924025 |
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Reference
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J:298768 Laugel-Haushalter V, Bar S, Schaefer E, Stoetzel C, Geoffroy V, Alembik Y, Kharouf N, Huckert M, Hamm P, Hemmerle J, Maniere MC, Friant S, Dollfus H, Bloch-Zupan A, A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. Front Genet. 2019;10:504 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E14.5 | E16.5 | E18.5 |
| Immunohistochemistry (section) | |||
| In situ RNA (section) | |
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| 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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