Q8N1N2 (CR026_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 54.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Uncharacterized protein C18orf26 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 210 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Membrane; Single-pass membrane protein Potential. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Membrane |
| Coding sequence diversity | Polymorphism |
| Domain | Transmembrane Transmembrane helix |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular component | integral to membrane Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 210 | 210 | Uncharacterized protein C18orf26 | PRO_0000079315 | |||||
Regions | |||||||||
| Transmembrane | 114 – 134 | 21 | Helical; Potential | ||||||
| Compositional bias | 172 – 207 | 36 | Thr-rich | ||||||
Natural variations | |||||||||
| Natural variant | 38 | 1 | V → A. Corresponds to variant rs35428499 [ dbSNP | Ensembl ]. | VAR_033751 | |||||
| Natural variant | 189 | 1 | T → P. Corresponds to variant rs9947055 [ dbSNP | Ensembl ]. | VAR_033752 | |||||
Sequences
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References
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Tongue. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK096425 mRNA. Translation: BAC04784.1. |
| IPI | IPI00166204. |
| RefSeq | NP_775900.1. NM_173629.1. |
| UniGene | Hs.376146. |
3D structure databases | |
| ProteinModelPortal | Q8N1N2. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q8N1N2. |
Polymorphism databases | |
| DMDM | 73620598. |
Proteomic databases | |
| PRIDE | Q8N1N2. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000321600; ENSP00000315265; ENSG00000178690. |
| GeneID | 284254. |
| KEGG | hsa:284254. |
| UCSC | uc002lfq.1. human. |
Organism-specific databases | |
| CTD | 284254. |
| GeneCards | GC18P052258. |
| HGNC | HGNC:26808. C18orf26. |
| HPA | HPA011148. |
| neXtProt | NX_Q8N1N2. |
| PharmGKB | PA134946407. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG17981. |
| GeneTree | ENSGT00400000022381. |
| InParanoid | Q8N1N2. |
| OMA | PGVLAHS. |
| OrthoDB | EOG42RD91. |
| PhylomeDB | Q8N1N2. |
Gene expression databases | |
| ArrayExpress | Q8N1N2. |
| Bgee | Q8N1N2. |
| CleanEx | HS_C18orf26. |
| Genevestigator | Q8N1N2. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| NextBio | 94661. |
Entry information
| Entry name | CR026_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8N1N2 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| 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 18 Human chromosome 18: 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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