Sequence Detail

ID/Version

Q8C170 Q8C0U0 Q4VBD3 Q80Y92 Q3TRT5 (UniProt | EBI)

Last sequence update: 2008-09-02
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=Unconventional myosin-IXa;AltName: Full=Unconventional myosin-9a;

Provider

SWISS-PROT

Sequence

Polypeptide 2542 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Myo9a	myosin IXa	26	102	4	22

Sequence references in MGI

J:56684 Gorman SW, et al., The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23. Genomics. 1999 Jul 15;59(2):150-60
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:251454 Abouhamed M, et al., Myosin IXa regulates epithelial differentiation and its deficiency results in hydrocephalus. Mol Biol Cell. 2009 Dec;20(24):5074-85
J:273536 O'Connor E, et al., Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome. Brain. 2016 Aug;139(Pt 8):2143-53
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89