SEC61A2 (SEC61 translocon subunit alpha 2)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 55176 |
| Gene name | SEC61 translocon subunit alpha 2 |
| Gene symbol | SEC61A2 |
| Synonyms (NCBI Gene) |
-
|
| Chromosome | 10 |
| Chromosome location | 10p14 |
| Summary | The protein encoded by this gene has similarity to a mouse protein which suggests a role in the insertion of secretory and membrane polypeptides into the endoplasmic reticulum. It may also be required for the assembly of membrane and secretory proteins. A |
|
miRNA
miRNA information provided by mirtarbase database.
200
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Protein
Protein information from UniProt database.
|
||||||||||||||||
|
UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
|
Q9H9S3 | |||||||||||||||
| Protein name | Protein transport protein Sec61 subunit alpha isoform 2 (Sec61 alpha-2) | |||||||||||||||
| Protein function | Component of SEC61 channel-forming translocon complex that mediates transport of signal peptide-containing precursor polypeptides across the endoplasmic reticulum (ER). Forms a ribosome receptor and a gated pore in the ER membrane, both function | |||||||||||||||
| Family and domains |
Pfam
|
|||||||||||||||
| Sequence | ||||||||||||||||
| Sequence length | 476 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
||||||||
|
||||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
|
|||||||||||||||||||||
|
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)
|
|||||||||||||||||||||
|
|||||||||||||||||||||