A6NGA9 (TM202_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 47.
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: Transmembrane protein 202 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Reference 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 | 273 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Membrane; Multi-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 – 273 | 273 | Transmembrane protein 202 | PRO_0000317201 | |||||
Regions | |||||||||
| Transmembrane | 53 – 75 | 23 | Helical; Potential | ||||||
| Transmembrane | 121 – 141 | 21 | Helical; Potential | ||||||
| Transmembrane | 155 – 175 | 21 | Helical; Potential | ||||||
| Transmembrane | 189 – 209 | 21 | Helical; Potential | ||||||
Natural variations | |||||||||
| Natural variant | 204 | 1 | M → L. Corresponds to variant rs16956904 [ dbSNP | Ensembl ]. | VAR_051434 | |||||
Sequences
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References
| [1] | "Analysis of the DNA sequence and duplication history of human chromosome 15." Zody M.C., Garber M., Sharpe T., Young S.K., Rowen L., O'Neill K., Whittaker C.A., Kamal M., Chang J.L., Cuomo C.A., Dewar K., FitzGerald M.G., Kodira C.D., Madan A., Qin S., Yang X., Abbasi N., Abouelleil A. Nusbaum C.Nature 440:671-675(2006) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AC079322 Genomic DNA. No translation available. |
| IPI | IPI00250368. |
| RefSeq | NP_001073931.1. NM_001080462.1. |
| UniGene | Hs.446069. |
3D structure databases | |
| ProteinModelPortal | A6NGA9. |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | A6NGA9. |
Proteomic databases | |
| PaxDb | A6NGA9. |
| PRIDE | A6NGA9. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000341689; ENSP00000340212; ENSG00000187806. |
| GeneID | 338949. |
| KEGG | hsa:338949. |
| UCSC | uc002auq.3. human. |
Organism-specific databases | |
| CTD | 338949. |
| GeneCards | GC15P072690. |
| HGNC | HGNC:33733. TMEM202. |
| HPA | HPA049035. |
| neXtProt | NX_A6NGA9. |
| PharmGKB | PA162406376. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG40198. |
| HOGENOM | HOG000090211. |
| HOVERGEN | HBG094967. |
| InParanoid | A6NGA9. |
| OMA | WSHTPKP. |
| OrthoDB | EOG49CQ87. |
| PhylomeDB | A6NGA9. |
Gene expression databases | |
| ArrayExpress | A6NGA9. |
| Bgee | A6NGA9. |
| CleanEx | HS_TMEM202. |
| Genevestigator | A6NGA9. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 338949. |
| NextBio | 97199. |
Entry information
| Entry name | TM202_HUMAN | ||||||||
| Accession | Primary (citable) accession number: A6NGA9 | ||||||||
| 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 15 Human chromosome 15: 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 |

Clusters with
