SNX7 (sorting nexin 7)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 51375 |
| Gene name | Sorting nexin 7 |
| Gene symbol | SNX7 |
| Synonyms (NCBI Gene) |
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| Chromosome | 1 |
| Chromosome location | 1p21.3 |
| Summary | This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like s |
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miRNA
miRNA information provided by mirtarbase database.
8
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
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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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Q9UNH6 | ||||||||||
| Protein name | Sorting nexin-7 | ||||||||||
| Protein function | Involved in the regulation of endocytosis and in several stages of intracellular trafficking (PubMed:32513819). Together with SNX4, involved in autophagosome assembly by regulating trafficking and recycling of phospholipid scramblase ATG9A (PubM | ||||||||||
| PDB | 3IQ2 | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 387 | ||||||||||
| Interactions | View interactions | ||||||||||
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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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