MYO19 (myosin XIX)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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80179 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Myosin XIX |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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MYO19 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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MYOHD1 |
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Chromosome
Chromosome number
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17 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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17q12 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q96H55 | ||||||||||
| Protein name | Unconventional myosin-XIX (Myosin head domain-containing protein 1) | ||||||||||
| Protein function | Actin-based motor molecule with ATPase activity that localizes to the mitochondrion outer membrane (PubMed:19932026, PubMed:23568824, PubMed:25447992). Motor protein that moves towards the plus-end of actin filaments (By similarity). Required fo | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed in multiple tissues and cell lines. {ECO:0000269|PubMed:19932026}. | ||||||||||
| Sequence |
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| Sequence length | 970 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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