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

Indicates gene expression was analyzed but not necessarily detected.

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