Reviewed,
UniProtKB/Swiss-Prot P0C862 (C1QT9_HUMAN)
Last modified
November 24, 2009.
Version 15.
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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: Complement C1q tumor necrosis factor-related protein 9 | ||||
| Gene names |
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| 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 | 333 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. |
| Sequence similarities | Contains 1 C1q domain. Contains 3 collagen-like domains. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Collagen Repeat Signal |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Cellular component | extracellular region Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 19 | 19 | Potential | ||||||
| Chain | 20 – 333 | 314 | Complement C1q tumor necrosis factor-related protein 9 | PRO_0000291751 | |||||
Regions | |||||||||
| Domain | 24 – 82 | 59 | Collagen-like 1 | ||||||
| Domain | 95 – 154 | 60 | Collagen-like 2 | ||||||
| Domain | 155 – 191 | 37 | Collagen-like 3 | ||||||
| Domain | 197 – 333 | 137 | C1q | ||||||
Natural variations | |||||||||
| Natural variant | 6 | 1 | L → F: dbSNP rs1974332. | VAR_059148 | |||||
| Natural variant | 219 | 1 | M → V: dbSNP rs3751357. Ref.1 Ref.2 Ref.3 | VAR_032840 | |||||
| Natural variant | 301 | 1 | V → M: dbSNP rs4589405. Ref.2 | VAR_032841 | |||||
Sequences
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References
| [1] | "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment." Clark H.F., Gurney A.L., Abaya E., Baker K., Baldwin D.T., Brush J., Chen J., Chow B., Chui C., Crowley C., Currell B., Deuel B., Dowd P., Eaton D., Foster J.S., Grimaldi C., Gu Q., Hass P.E. Gray A.M.Genome Res. 13:2265-2270(2003) [PubMed: 12975309] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219. |
| [2] | "The DNA sequence and analysis of human chromosome 13." Dunham A., Matthews L.H., Burton J., Ashurst J.L., Howe K.L., Ashcroft K.J., Beare D.M., Burford D.C., Hunt S.E., Griffiths-Jones S., Jones M.C., Keenan S.J., Oliver K., Scott C.E., Ainscough R., Almeida J.P., Ambrose K.D., Andrews D.T. Ross M.T.Nature 428:522-528(2004) [PubMed: 15057823] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], VARIANTS VAL-219 AND MET-301. |
| [3] | "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: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT VAL-219. |
Cross-references
Sequence databases | |
|---|---|
| AY358145 mRNA. Translation: AAQ88512.1. AL359736 Genomic DNA. Translation: CAH72292.1. AL359736 Genomic DNA. Translation: CAH72293.1. BC040438 mRNA. Translation: AAH40438.1. | |
| IPI | IPI00552240. |
| RefSeq | NP_848635.2. |
| UniGene | Hs.362854 |
3D structure databases | |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | P0C862. |
Genome annotation databases | |
| Ensembl | ENST00000332018; ENSP00000333737; ENSG00000240654; Homo sapiens. [Genome view] ENST00000382071; ENSP00000371503; ENSG00000240654; Homo sapiens. [Genome view] |
| GeneID | 338872. |
| KEGG | hsa:338872. |
Organism-specific databases | |
| CTD | 338872. |
| GeneCards | GC13P023779. |
| HGNC | HGNC:28732. C1QTNF9. |
| GenAtlas | Search... |
Phylogenomic databases | |
| OMA | CHVAGVY |
Gene expression databases | |
| ArrayExpress | P0C862. |
| Bgee | P0C862. |
| CleanEx | HS_C1QTNF9. |
| Genevestigator | P0C862. |
Family and domain databases | |
| InterPro | IPR001073. C1q. IPR008160. Collagen. IPR008983. Tumour_necrosis_fac-like. [Graphical view] |
| Gene3D | G3DSA:2.60.120.40. Tumour_necrosis_fac-like. 1 hit. |
| Pfam | PF00386. C1q. 1 hit. PF01391. Collagen. 3 hits. [Graphical view] |
| PRINTS | PR00007. COMPLEMNTC1Q. |
| SMART | SM00110. C1Q. 1 hit. [Graphical view] |
| PROSITE | PS50871. C1Q. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Entry information
| Entry name | C1QT9_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P0C862 Secondary accession number(s): A2A3T6 Q8IUU4 | ||||||||
| 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 |
| SIMILARITY comments Index of protein domains and families |

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