STX10 (syntaxin 10)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 8677 |
| Gene name | Syntaxin 10 |
| Gene symbol | STX10 |
| Synonyms (NCBI Gene) |
SYN10hsyn10
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| Chromosome | 19 |
| Chromosome location | 19p13.13 |
| Summary | This gene belongs to the syntaxin family and encodes a soluble N-ethylmaleimide sensitive factor attachment protein receptor (SNARE). The encoded protein is involved in docking and fusion events at the Golgi apparatus. Alternative splicing results in mult |
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miRNA
miRNA information provided by mirtarbase database.
2
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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O60499 | |||||||||||||||
| Protein name | Syntaxin-10 (Syn10) | |||||||||||||||
| Protein function | SNARE involved in vesicular transport from the late endosomes to the trans-Golgi network. | |||||||||||||||
| PDB | 4DND | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed at high levels in heart, skeletal muscle and pancreas. | |||||||||||||||
| Sequence |
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| Sequence length | 249 | |||||||||||||||
| 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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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