Reviewed,
UniProtKB/Swiss-Prot P58512 (CU067_HUMAN)
Last modified
December 15, 2009.
Version 47.
History...
Clusters with 100%,
90%,
50% identity |
Documents (1) |
Third-party data |
Customize display | text xml rdf/xml gff fasta |
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 C21orf67 | ||
| 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 | 204 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Tissue specificity | Not detected in any tissue tested. |
| Caution | Maps to the wrongly predicted PRED54 locus. |
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: P58512-1) 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: P58512-2) The sequence of this isoform differs from the canonical sequence as follows: 72-82: LAADLAGDALP → CTSGASAGQKL 83-204: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 204 | 204 | Uncharacterized protein C21orf67 | PRO_0000079526 | |||||
Natural variations | |||||||||
| Alternative sequence | 72 – 82 | 11 | LAADLAGDALP → CTSGASAGQKL in isoform B. | VSP_003829 | |||||
| Alternative sequence | 83 – 204 | 122 | Missing in isoform B. | VSP_003830 | |||||
Sequences
| ||||||||||||||||||||||||
References
| [1] | "From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map." Reymond A., Friedli M., Neergaard Henrichsen C., Chapot F., Deutsch S., Ucla C., Rossier C., Lyle R., Guipponi M., Antonarakis S.E. Genomics 78:46-54(2001) [PubMed: 11707072] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS A AND B). |
Cross-references
Sequence databases | |
|---|---|
| AF380178 mRNA. Translation: AAL34496.1. AY040088 mRNA. Translation: AAK74136.1. | |
| IPI | IPI00067917. IPI00219867. |
| UniGene | Hs.534504 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | P58512. |
Proteomic databases | |
| PRIDE | P58512. |
Genome annotation databases | |
| Ensembl | ENST00000330551; ENSP00000331610; ENSG00000183250; Homo sapiens. [Genome view] |
| UCSC | uc002zgj.2. human. |
Organism-specific databases | |
| GeneCards | GC21M045181. GC21M045182. |
| HGNC | HGNC:15707. C21orf67. |
| PharmGKB | PA25862. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | P58512. |
| OMA | PSPIRNC. |
Gene expression databases | |
| ArrayExpress | P58512. |
| Bgee | P58512. |
| CleanEx | HS_C21orf67. |
| Genevestigator | P58512. |
| GermOnline | ENSG00000183250. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Entry information
| Entry name | CU067_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P58512 | ||||||||
| 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 |

Clusters with


