Symbol Name ID |
Slc7a8
solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 MGI:1355323 |
Reference
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J:151324 Wirth EK, Roth S, Blechschmidt C, Holter SM, Becker L, Racz I, Zimmer A, Klopstock T, Gailus-Durner V, Fuchs H, Wurst W, Naumann T, Brauer A, de Angelis MH, Kohrle J, Gruters A, Schweizer U, Neuronal 3',3,5-triiodothyronine (T3) uptake and behavioral phenotype of mice deficient in Mct8, the neuronal T3 transporter mutated in Allan-Herndon-Dudley syndrome. J Neurosci. 2009 Jul 29;29(30):9439-49 |
Age | E14 | E17 | 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 11/19/2024 MGI 6.24 |
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