Reviewed,
UniProtKB/Swiss-Prot Q96KW9 (CM028_HUMAN)
Last modified
November 24, 2009.
Version 45.
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: Putative uncharacterized protein C13orf28 | ||
| 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 | 195 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Signal |
| PTM | Glycoprotein |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Cellular component | extracellular region 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 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 24 | 24 | Potential | ||||||
| Chain | 25 – 195 | 171 | Putative uncharacterized protein C13orf28 | PRO_0000274330 | |||||
Amino acid modifications | |||||||||
| Glycosylation | 62 | 1 | N-linked (GlcNAc...) Potential | ||||||
| Glycosylation | 159 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 25 | 1 | R → W in a colorectal cancer sample; somatic mutation. Ref.3 | VAR_035675 | |||||
| Natural variant | 111 | 1 | V → D: dbSNP rs10816. Ref.2 | VAR_030260 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AL160033 Genomic DNA. Translation: CAI14451.1. BC016750 mRNA. Translation: AAH16750.1. | |
| IPI | IPI00747019. |
| RefSeq | NP_660291.1. |
| UniGene | Hs.97592 |
3D structure databases | |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | Q96KW9. |
Genome annotation databases | |
| Ensembl | ENST00000283550; ENSP00000283550; ENSG00000153498; Homo sapiens. [Genome view] |
| GeneID | 122258. |
| KEGG | hsa:122258. |
| NMPDR | fig|9606.3.peg.9100. |
| UCSC | uc001vsd.1. human. |
Organism-specific databases | |
| CTD | 122258. |
| GeneCards | GC13P112079. |
| HGNC | HGNC:29575. C13orf28. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOVERGEN | Q96KW9. |
| OrthoDB | EOG9XH2JZ |
Gene expression databases | |
| ArrayExpress | Q96KW9. |
| Bgee | Q96KW9. |
| CleanEx | HS_C13orf28. |
| Genevestigator | Q96KW9. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 80869. |
Entry information
| Entry name | CM028_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q96KW9 Secondary accession number(s): Q5T8L1 | ||||||||
| 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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