Symbol Name ID |
Atp13a4
ATPase type 13A4 MGI:1924456 |
Age | E7 | E11 | E15 | E17 | P |
RT-PCR | 1 | 1 | 1 | 1 | 2 |
Atp13a4 ATPase type 13A4 (Synonyms: 4631413J11Rik, 9330174J19Rik) | |
Results | Reference |
1* | J:193641 Nakano Y, Jahan I, Bonde G, Sun X, Hildebrand MS, Engelhardt JF, Smith RJ, Cornell RA, Fritzsch B, Banfi B, A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse. PLoS Genet. 2012;8(10):e1002966 |
5* | J:159343 Vallipuram J, Grenville J, Crawford DA, The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation. Cell Mol Neurobiol. 2010 Mar;30(2):233-46 |
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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