Q96NL6 (SCLT1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 73.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Sodium channel and clathrin linker 1 Alternative name(s): Sodium channel-associated protein 1 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 688 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Function | Adapter protein that links SCN10A to clathrin. Regulates SCN10A channel activity, possibly by promoting channel internalization By similarity. |
| Subunit structure | Interacts with SCN10A and clathrin. Identified in a complex containing SCN10A, clathrin and SCLT1 By similarity. |
| Subcellular location | Cytoplasm. Note: Cell periphery By similarity. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Cytoplasm |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Biological_process | clustering of voltage-gated sodium channels Inferred from electronic annotation. Source: Compara |
| Cellular_component | centrosome Inferred from direct assay PubMed 21399614. Source: UniProtKB clathrin complexInferred from electronic annotation. Source: Compara cytoplasmInferred from direct assay. Source: HPA intermediate filament cytoskeletonInferred from direct assay. Source: HPA |
| Molecular_function | sodium channel regulator activity Inferred from electronic annotation. Source: Compara |
| Complete GO annotation... | |
Alternative products
| This entry describes 4 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q96NL6-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q96NL6-2) The sequence of this isoform differs from the canonical sequence as follows: 230-610: Missing. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 3 (identifier: Q96NL6-3) The sequence of this isoform differs from the canonical sequence as follows: 98-610: Missing. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 4 (identifier: Q96NL6-4) The sequence of this isoform differs from the canonical sequence as follows: 79-79: K → A 80-688: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 688 | 688 | Sodium channel and clathrin linker 1 | PRO_0000317127 | |||||
Regions | |||||||||
| Coiled coil | 69 – 673 | 605 | Potential | ||||||
Natural variations | |||||||||
| Alternative sequence | 79 | 1 | K → A in isoform 4. | VSP_030904 | |||||
| Alternative sequence | 80 – 688 | 609 | Missing in isoform 4. | VSP_030905 | |||||
| Alternative sequence | 98 – 610 | 513 | Missing in isoform 3. | VSP_030906 | |||||
| Alternative sequence | 230 – 610 | 381 | Missing in isoform 2. | VSP_030907 | |||||
| Natural variant | 441 | 1 | S → C. Ref.1 Ref.3 Corresponds to variant rs10028124 [ dbSNP | Ensembl ]. | VAR_038481 | |||||
Sequences
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References
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT CYS-441. |
| [2] | "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C., Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L., Du H. Wilson R.K.Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANT CYS-441. |
| [4] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 2; 3 AND 4). Tissue: Lung. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK055217 mRNA. Translation: BAB70876.1. AC093783 Genomic DNA. No translation available. AC093826 Genomic DNA. No translation available. CH471056 Genomic DNA. Translation: EAX05167.1. BC064428 mRNA. Translation: AAH64428.1. BC121057 mRNA. Translation: AAI21058.1. BC121058 mRNA. Translation: AAI21059.1. BC128051 mRNA. Translation: AAI28052.1. |
| IPI | IPI00043740. IPI00884940. IPI00885137. IPI00885162. |
| RefSeq | NP_653244.2. NM_144643.2. |
| UniGene | Hs.654690. |
3D structure databases | |
| HSSP | HSSP built from PDB template 1X79 based on UniProtKB Q15276. |
| ProteinModelPortal | Q96NL6. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q96NL6. 5 interactions. |
| STRING | 9606.ENSP00000281142. |
PTM databases | |
| PhosphoSite | Q96NL6. |
Polymorphism databases | |
| DMDM | 300669665. |
Proteomic databases | |
| PaxDb | Q96NL6. |
| PRIDE | Q96NL6. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000281142; ENSP00000281142; ENSG00000151466. ENST00000434680; ENSP00000401539; ENSG00000151466. ENST00000439369; ENSP00000395292; ENSG00000151466. ENST00000511426; ENSP00000420861; ENSG00000151466. |
| GeneID | 132320. |
| KEGG | hsa:132320. |
| UCSC | uc003ign.2. human. uc003igq.2. human. uc003igt.4. human. uc010iob.1. human. |
Organism-specific databases | |
| CTD | 132320. |
| GeneCards | GC04M129805. |
| H-InvDB | HIX0004499. |
| HGNC | HGNC:26406. SCLT1. |
| HPA | HPA036561. |
| MIM | 611399. gene. |
| neXtProt | NX_Q96NL6. |
| PharmGKB | PA147357369. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG121178. |
| HOGENOM | HOG000154268. |
| HOVERGEN | HBG098335. |
| InParanoid | Q96NL6. |
| OMA | RRYQMEN. |
| OrthoDB | EOG44QT17. |
| PhylomeDB | Q96NL6. |
Gene expression databases | |
| ArrayExpress | Q96NL6. |
| Bgee | Q96NL6. |
| CleanEx | HS_SCLT1. |
| Genevestigator | Q96NL6. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| ChiTaRS | SCLT1. human. |
| GenomeRNAi | 132320. |
| NextBio | 83079. |
| SOURCE | Search... |
Entry information
| Entry name | SCLT1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96NL6 Secondary accession number(s): A4QN04, Q0VAH2, Q6P2M4 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 4 Human chromosome 4: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |

Clusters with
