SEC31B (SEC31 homolog B, COPII component)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 25956 |
| Gene name | SEC31 homolog B, COPII component |
| Gene symbol | SEC31B |
| Synonyms (NCBI Gene) |
SEC31B-1SEC31L2
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| Chromosome | 10 |
| Chromosome location | 10q24.31 |
| Summary | This gene encodes a protein of unknown function. The protein has moderate similarity to rat VAP1 protein which is an endosomal membrane-associated protein, containing a putative Ca2+/calmodulin-dependent kinase II phosphorylation site. [provided by RefSeq |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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Q9NQW1 |
| Protein name | Protein transport protein Sec31B (SEC31-like protein 2) (SEC31-related protein B) (SEC31B-1) |
| Protein function | As a component of the coat protein complex II (COPII), may function in vesicle budding and cargo export from the endoplasmic reticulum. |
| Family and domains | |
| Tissue specificity | TISSUE SPECIFICITY: Ubiquitously expressed at low levels with specific expression in thymus and testis. Expressed in testis by Sertoli cells, Leydig cells and spermatogonia and in cerebellum more prominently by Purkinje and granular cells (at protein leve |
| Sequence |
MKLKELERPAVQAWSPASQYPLYLATGTSAQQLDSSFSTNGTLEIFEVDFRDPSLDLKHR |
| Sequence length | 1179 |
| 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.).
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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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Related Genes
Genes most often co-reported with SEC31B across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to SEC31B (see Related Genes above), that are NOT already directly curated for SEC31B itself -- a lead worth checking, not a confirmed association.
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