Reviewed,
UniProtKB/Swiss-Prot Q6ICL3 (CV025_HUMAN)
Last modified
October 13, 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: Uncharacterized protein C22orf25 | ||
| 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 | 276 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 |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 3 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q6ICL3-1) 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 2 (identifier: Q6ICL3-2) The sequence of this isoform differs from the canonical sequence as follows: 90-151: Missing. | ||||||
| Isoform 3 (identifier: Q6ICL3-3) The sequence of this isoform differs from the canonical sequence as follows: 1-48: MCIIFFKFDP...FWGNNNEILS → MPLGAGTPVN...FWGNNNEILS 190-197: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 276 | 276 | Uncharacterized protein C22orf25 | PRO_0000253891 | |||||
Natural variations | |||||||||
| Alternative sequence | 1 – 48 | 48 | MCIIF…NEILS → MPLGAGTPVNVQRREDSATE GSHRLILAANRDEFYSRPSK LADFWGNNNEILS in isoform 3. | VSP_021137 | |||||
| Alternative sequence | 90 – 151 | 62 | Missing in isoform 2. | VSP_021139 | |||||
| Alternative sequence | 190 – 197 | 8 | Missing in isoform 3. | VSP_021138 | |||||
| Natural variant | 125 | 1 | D → N: dbSNP rs17855650. Ref.3 | VAR_028742 | |||||
| Natural variant | 200 | 1 | E → K: dbSNP rs17854107. Ref.3 | VAR_028743 | |||||
| Natural variant | 245 | 1 | D → E: dbSNP rs16982614. | VAR_028744 | |||||
Sequences
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References
Cross-references
Entry information
| Entry name | CV025_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q6ICL3 Secondary accession number(s): Q8IW05 Q96M16 | ||||||||
| Entry history |
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| 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 22 Human chromosome 22: 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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