Reviewed,
UniProtKB/Swiss-Prot Q9BR26 (CT123_HUMAN)
Last modified
November 24, 2009.
Version 42.
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: Transmembrane protein C20orf123 | ||
| 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 | 566 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Subcellular location | Membrane; Multi-pass membrane protein Potential. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Cellular component | integral to membrane 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 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 566 | 566 | Transmembrane protein C20orf123 | PRO_0000342121 | |||||
Regions | |||||||||
| Transmembrane | 52 – 72 | 21 | Potential | ||||||
| Transmembrane | 82 – 102 | 21 | Potential | ||||||
| Transmembrane | 129 – 149 | 21 | Potential | ||||||
| Transmembrane | 228 – 248 | 21 | Potential | ||||||
| Transmembrane | 305 – 325 | 21 | Potential | ||||||
| Transmembrane | 342 – 362 | 21 | Potential | ||||||
| Transmembrane | 399 – 419 | 21 | Potential | ||||||
| Compositional bias | 59 – 63 | 5 | Poly-Ala | ||||||
Natural variations | |||||||||
| Natural variant | 565 | 1 | P → S: dbSNP rs847079. | VAR_050919 | |||||
Sequences
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References
| [1] | "The DNA sequence and comparative analysis of human chromosome 20." Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. Rogers J.Nature 414:865-871(2001) [PubMed: 11780052] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
Cross-references
Sequence databases | |
|---|---|
| AL034424 Genomic DNA. Translation: CAC36102.2. | |
| IPI | IPI00552151. |
| RefSeq | NP_542452.1. |
| UniGene | Hs.526636 |
3D structure databases | |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | Q9BR26. |
Genome annotation databases | |
| Ensembl | ENST00000279028; ENSP00000279028; ENSG00000149635; Homo sapiens. [Genome view] |
| GeneID | 128506. |
| KEGG | hsa:128506. |
Organism-specific databases | |
| CTD | 128506. |
| GeneCards | GC20M044603. |
| HGNC | HGNC:16116. C20orf123. |
| PharmGKB | PA25664. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q9BR26. |
| OMA | WYLHRYL |
| OrthoDB | EOG9SJ80N |
Gene expression databases | |
| ArrayExpress | Q9BR26. |
| Bgee | Q9BR26. |
| CleanEx | HS_C20orf123. |
| Genevestigator | Q9BR26. |
Family and domain databases | |
| InterPro | IPR012858. DC_STAMP. [Graphical view] |
| Pfam | PF07782. DC_STAMP. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 82378. |
Entry information
| Entry name | CT123_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9BR26 | ||||||||
| 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 20 Human chromosome 20: 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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