Slc10a7 cDNA1
Probe Detail
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Name
Slc10a7 cDNA1
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Sequence Type
cDNA
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ID
MGI:6505318
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Insert Size
0.918kb
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Note
GAACATGGTTGGTCTTAGAGGCATAGTCTACAAGGATGCCTCCTATTCACAGACTGTAAG
AGCAACCGGACTTTAAATTTATTTCTACCCTTCATCTGCTGGATGACCTTGGGCAAGTCA
TTTTAATATCCCTAGCTGCCAGTCACAATTTATTAAATATTATAATTAAAGTACCTCAAG
GTATTATTGTGAACTATTGACGGGTGTAAAGTTCTTGCAGTATAGTCTGACACAATGAAC
ACTCTATGTCGTCACTTGTCATCATCGTCATCATTATCATCATCACCACATTGTTTGTGT
ATGCCAAACAGGAAGCAACCCTTTCAAATGTGGTCCATAAATATGACATCCATACACATA
GTGCTTAGTGCTGTCTTCAATGGGGTTCTGTTGGCGGAAGATTCTGAGGCAGGTTGAATA
CAAGAAATGCATAGGGGTGAAAGGAGCAGGGAGGGGAAGCTGTTTCCCACCAAAGCCTTC
CACAGCCTGTCCTAATGCCTCTCTCTGGGGCTGGGCCGACTCCTCTGAGTGGTTAGTCTT
CATGTTTTCTCACAGTCATTTCAGGCTGGCCTCACTCAAACCCATAGGAAAGAAGCAGCA
AACAGAGCAGGTAGATCCATACAGAACACCATAGCAGCCACCACACAGACACTCTTACAA
TTAACTTTAAACTTAGAAAATAGGCTAAATTTAGTGTAATTGGGGTGATTTAAAAGCAATCAAAGATTProbe sequence:
ATGACTTCATTAAATACAAAATAAAATTGAAAAATACATCCCCATGCCAATTACATAATG
AGGATTTTGAATAACCATTTGCCCTGCTGCCTCTGTAGCCTCTGCTCTGTTTCTCACCTG
ACTCACCTGGACCTTTCTCAGTCTCCGTTCATTCCTTCGGATGGAGCTCACTCCTGCCCA
CCTCCCACCCAGCTTATTACTCGCCTGACTCTTGAACTCACCTCTCATTTGAACGG
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Species
mouse, laboratory
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Slc10a7
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solute carrier family 10 (sodium/bile acid cotransporter family), member 7
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J:298768
Laugel-Haushalter V, et al., A New SLC10A7 Homozygous Missense Mutation Responsible for a Milder Phenotype of Skeletal Dysplasia With Amelogenesis Imperfecta. Front Genet. 2019;10:504
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