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Gene Expression Literature Detail
Symbol
Name
ID
Slc10a7
solute carrier family 10 (sodium/bile acid cotransporter family), member 7
MGI:1924025

Reference
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

Detailed expression data for these assays: 17 results

red ball Indicates gene expression was analyzed but not necessarily detected.
Age E12.5 E14.5 E16.5 P
Immunohistochemistry (section)
In situ RNA (section) red ball red ball red ball red ball
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


Contributing Projects:
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
The Jackson Laboratory