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Gene Expression Literature Summary
Symbol
Name
ID
Atp13a4
ATPase type 13A4
MGI:1924456

2 matching records from 2 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.
Age E7 E11 E15 E17 P
RT-PCR 1 1 1 1 2

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available
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

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
04/16/2024
MGI 6.23
The Jackson Laboratory