Reviewed,
UniProtKB/Swiss-Prot Q6NSX1 (CCD70_HUMAN)
Last modified
November 24, 2009.
Version 56.
History...
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Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Coiled-coil domain-containing protein 70 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Complete 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 | 233 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Subcellular location | Secreted Potential. |
| Caution | It is uncertain whether Met-1 or Met-12 is the initiator. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Coiled coil Signal |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Cellular component | extracellular region Inferred from electronic annotation. Source: UniProtKB-SubCell plasma membraneInferred from direct assay. Source: LIFEdb |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 32 | 32 | Potential | ||||||
| Chain | 33 – 233 | 201 | Coiled-coil domain-containing protein 70 | PRO_0000234432 | |||||
Regions | |||||||||
| Coiled coil | 140 – 164 | 25 | Potential | ||||||
Natural variations | |||||||||
| Natural variant | 126 | 1 | R → C: dbSNP rs17076052. | VAR_050763 | |||||
| Natural variant | 206 | 1 | I → V: dbSNP rs1054515. Ref.1 Ref.2 Ref.4 | VAR_026238 | |||||
Experimental info | |||||||||
| Sequence conflict | 232 | 1 | R → G in BAC05391. Ref.2 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AL136887 mRNA. Translation: CAB66821.1. AK098719 mRNA. Translation: BAC05391.1. AL162377 Genomic DNA. Translation: CAI13430.1. BC069691 mRNA. Translation: AAH69691.1. BC069748 mRNA. Translation: AAH69748.1. BC069770 mRNA. Translation: AAH69770.1. BC069806 mRNA. Translation: AAH69806.1. | |
| IPI | IPI00550289. |
| RefSeq | NP_112580.2. |
| UniGene | Hs.120573 |
3D structure databases | |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | Q6NSX1. |
Genome annotation databases | |
| Ensembl | ENST00000242819; ENSP00000242819; ENSG00000123171; Homo sapiens. [Genome view] |
| GeneID | 83446. |
| KEGG | hsa:83446. |
| UCSC | uc001vfu.2. human. |
Organism-specific databases | |
| CTD | 83446. |
| GeneCards | GC13P051335. |
| HGNC | HGNC:25303. CCDC70. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | Q6NSX1. |
| HOVERGEN | Q6NSX1. |
| OMA | EEEKTFW |
| OrthoDB | EOG9VX4RK |
Gene expression databases | |
| ArrayExpress | Q6NSX1. |
| Bgee | Q6NSX1. |
| CleanEx | HS_CCDC70. |
| Genevestigator | Q6NSX1. |
| GermOnline | ENSG00000123171. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 72344. |
Entry information
| Entry name | CCD70_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q6NSX1 Secondary accession number(s): Q8N7A8, Q9H097 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 13 Human chromosome 13: 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 |

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