Reviewed,
UniProtKB/Swiss-Prot Q9NZP6 (CO002_HUMAN)
Last modified
July 22, 2008.
Version 31.
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: Protein C15orf2 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 1156 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Function | May be involved in spermatogenesis. |
| Tissue specificity | Testis-specific in adults. |
Ontologies
Keywords | |
|---|---|
| Biological process | Differentiation Spermatogenesis |
| Coding sequence diversity | Polymorphism |
| Molecular function | Developmental protein |
Gene Ontology (GO) | |
| Biological process | spermatogenesis Ref.1 Non-traceable author statement. Source: UniProtKB |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | ||||
Molecule processing | ||||||||
|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1156 | 1156 | Protein C15orf2 | |||||
Regions | ||||||||
| Compositional bias | 285 – 536 | 252 | Pro-rich | |||||
Natural variations | ||||||||
| Natural variant | 37 | 1 | R → Q in a colorectal cancer sample; somatic mutation. | |||||
| Natural variant | 114 | 1 | V → I in a colorectal cancer sample; somatic mutation. | |||||
| Natural variant | 212 | 1 | V → A: dbSNP rs3784246. | |||||
| Natural variant | 253 | 1 | G → R: dbSNP rs1563102. | |||||
| Natural variant | 282 | 1 | N → S: dbSNP rs7165533. | |||||
| Natural variant | 406 | 1 | Q → E: dbSNP rs3742950. | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AF179681 Genomic DNA. Translation: AAF72107.1. AC100720 Genomic DNA. No translation available. | |
| RefSeq | NP_061831.2. |
| UniGene | Hs.649663 |
3D structure databases | |
| ModBase | Search... |
Genome annotation databases | |
| Ensembl | ENSG00000185823. Homo sapiens. [Contig view] |
| GeneID | 23742. |
| KEGG | hsa:23742. |
| NMPDR | fig|9606.3.peg.10362. |
Organism-specific databases | |
| HGNC | HGNC:1190. C15orf2. |
| MIM | 610922. gene. |
| PharmGKB | PA25519. |
| GenAtlas | Search... |
| GeneCards | Search... |
| GeneLynx | Search... |
Phylogenomic databases | |
| HOGENOM | Q9NZP6. |
| HOVERGEN | Q9NZP6. |
Gene expression databases | |
| ArrayExpress | Q9NZP6. |
| CleanEx | HS_C15orf2. |
| GermOnline | ENSG00000185823. Homo sapiens. |
Family and domain databases | |
| ProDom | Q9NZP6. [Graphical view] [Entries sharing at least one domain] |
| BLOCKS | Search... |
Other Resources | |
| LinkHub | Q9NZP6. |
| SOURCE | Search... |
| ProtoNet | Search... |
Entry information
| Entry name | CO002_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NZP6 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 15 Human chromosome 15: 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 |

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