Reviewed,
UniProtKB/Swiss-Prot Q5T0U0 (CC122_HUMAN)
Last modified
December 15, 2009.
Version 37.
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Names and origin · Protein attributes · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Coiled-coil domain-containing protein 122 | ||
| 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 | 273 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q5T0U0-1) 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. | ||||||
| Note: No experimental confirmation available. | ||||||
| Isoform 2 (identifier: Q5T0U0-2) The sequence of this isoform differs from the canonical sequence as follows: 225-273: VQHKRYDAIL...ELRKCIGMQE → GLAPSPRLEC...IFSRDGVSPC |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 273 | 273 | Coiled-coil domain-containing protein 122 | PRO_0000286598 | |||||
Regions | |||||||||
| Coiled coil | 24 – 116 | 93 | Potential | ||||||
| Coiled coil | 179 – 269 | 91 | Potential | ||||||
Natural variations | |||||||||
| Alternative sequence | 225 – 273 | 49 | VQHKR…IGMQE → GLAPSPRLECSSAISAHCKL CLPGSRHSPASASGVAGTTG ACHHTQLIFCIFSRDGVSPC in isoform 2. | VSP_025114 | |||||
| Natural variant | 269 | 1 | I → T: dbSNP rs9567280. | VAR_061579 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AK056408 mRNA. Translation: BAB71178.1. AL512506 Genomic DNA. Translation: CAI16114.1. BC137289 mRNA. Translation: AAI37290.1. BC137290 mRNA. Translation: AAI37291.1. BC144570 mRNA. Translation: AAI44571.1. | |
| IPI | IPI00043427. IPI00845265. |
| RefSeq | NP_659411.2. |
| UniGene | Hs.170849 |
3D structure databases | |
| ModBase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000281508; ENSP00000281508; ENSG00000151773; Homo sapiens. [Genome view] ENST00000379193; ENSP00000368491; ENSG00000151773; Homo sapiens. [Genome view] ENST00000444614; ENSP00000407763; ENSG00000151773; Homo sapiens. [Genome view] |
| GeneID | 160857. |
| KEGG | hsa:160857. |
| UCSC | uc010acf.1. human. |
Organism-specific databases | |
| CTD | 160857. |
| GeneCards | GC13M043309. |
| HGNC | HGNC:26478. CCDC122. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q5T0U0. |
| OMA | QEDITKL. |
| OrthoDB | EOG9Z657D. |
Gene expression databases | |
| ArrayExpress | Q5T0U0. |
| Bgee | Q5T0U0. |
| CleanEx | HS_CCDC122. |
| Genevestigator | Q5T0U0. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 88007. |
Entry information
| Entry name | CC122_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q5T0U0 Secondary accession number(s): B2RP70, B7ZMI9, Q96MV0 | ||||||||
| 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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