Reviewed,
UniProtKB/Swiss-Prot P58505 (CU058_HUMAN)
Last modified
November 24, 2009.
Version 52.
History...
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Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Uncharacterized protein C21orf58 | ||
| 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 | 322 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 |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform A (identifier: P58505-1) 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. | ||||||
| Isoform B (identifier: P58505-2) The sequence of this isoform differs from the canonical sequence as follows: 273-277: PPHVP → RFFHS 278-322: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 322 | 322 | Uncharacterized protein C21orf58 | PRO_0000079521 | |||||
Regions | |||||||||
| Compositional bias | 292 – 299 | 8 | Poly-His | ||||||
Natural variations | |||||||||
| Alternative sequence | 273 – 277 | 5 | PPHVP → RFFHS in isoform B. | VSP_003827 | |||||
| Alternative sequence | 278 – 322 | 45 | Missing in isoform B. | VSP_003828 | |||||
Experimental info | |||||||||
| Sequence conflict | 111 | 1 | N → D in BAG51693. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AK056387 mRNA. Translation: BAG51693.1. AP000471 Genomic DNA. No translation available. AY039243 mRNA. Translation: AAK72408.1. Different initiation. AY039244 mRNA. Translation: AAK72409.1. Different initiation. | |
| IPI | IPI00291921. IPI00396359. |
| RefSeq | NP_478060.2. |
| UniGene | Hs.236572 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | P58505. 1 interaction. |
| STRING | P58505. |
Genome annotation databases | |
| Ensembl | ENST00000291691; ENSP00000291691; ENSG00000160298; Homo sapiens. [Genome view] |
| GeneID | 54058. |
| KEGG | hsa:54058. |
| UCSC | uc002ziz.2. human. uc002zjf.1. human. |
Organism-specific databases | |
| CTD | 54058. |
| GeneCards | GC21M046545. |
| HGNC | HGNC:1300. C21orf58. |
| PharmGKB | PA25853. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | P58505. |
| HOVERGEN | P58505. |
| OMA | HQILMQN |
Enzyme and pathway databases | |
| BioCyc | CATTLE:ENSBTAG00000021984-MON. |
Gene expression databases | |
| ArrayExpress | P58505. |
| Bgee | P58505. |
| CleanEx | HS_C21orf58. |
| Genevestigator | P58505. |
| GermOnline | ENSG00000160298. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 56364. |
Entry information
| Entry name | CU058_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P58505 Secondary accession number(s): B3KPI1 | ||||||||
| 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 21 Human chromosome 21: entries, gene names and cross-references to MIM |

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