Reviewed,
UniProtKB/Swiss-Prot Q9NRJ1 (MOST1_HUMAN)
Last modified
July 22, 2008.
Version 25.
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: Protein MOST-1 | ||
| 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 | 99 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at protein level. |
General annotation (Comments)
| Function | May be involved in cell survival, proliferation and progression of cancer cells. |
| Subunit structure | Interacts with TSPO, IGHM and IGHD. |
| Subcellular location | Cytoplasm. Microsome membrane. Endoplasmic reticulum membrane. |
| Tissue specificity | Expressed in the heart, kidney, liver, pancreas, small intestine, ovary, testis, prostate and thymus. Expressed in all of the cancer cell lines tested. |
Ontologies
Keywords | |
|---|---|
| Cellular component | Cytoplasm Endoplasmic reticulum Membrane Microsome |
| Coding sequence diversity | Polymorphism |
Gene Ontology (GO) | |
| Cellular component | endoplasmic reticulum membrane Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Complete GO annotation... | |
Sequence annotation (Features)
Sequences
References
| « Hide 'large scale' references | |
| [1] | "The novel human MOST-1 (C8orf17) gene exhibits tissue specific expression, maps to chromosome 8q24.2, and is overexpressed/amplified in high grade cancers of the breast and prostate." Tan J.M.M., Tock E.P.C., Chow V.T.K. Mol. Pathol. 56:109-115(2003) [PubMed: 12665628] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, TISSUE SPECIFICITY. |
| [2] | Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., Turner R. Venter J.C.Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | "Cellular expression, localization and interactions of the product of the human MOST-1 gene associated with breast and prostate cancers." Tan J.M.M., Chow V.T.K. Int. J. Oncol. 30:81-89(2007) [PubMed: 17143515] [Abstract] Cited for: SUBCELLULAR LOCATION, INTERACTION WITH TSPO, IGHM AND IGHD. |
Cross-references
Sequence databases | |
|---|---|
| AF220264 mRNA. Translation: AAF87328.1. CH471060 Genomic DNA. Translation: EAW92204.1. | |
| UniGene | Hs.283098 |
3D structure databases | |
| ModBase | Search... |
Genome annotation databases | |
| Ensembl | ENSG00000211505. Homo sapiens. [Contig view] |
Organism-specific databases | |
| HGNC | HGNC:17737. C8orf17. |
| PharmGKB | PA25960. |
| GenAtlas | Search... |
| GeneCards | Search... |
Phylogenomic databases | |
| HOVERGEN | Q9NRJ1. |
Gene expression databases | |
| ArrayExpress | Q9NRJ1. |
| CleanEx | HS_C8orf17. |
Family and domain databases | |
| ProDom | Q9NRJ1. [Graphical view] [Entries sharing at least one domain] |
| BLOCKS | Search... |
Other Resources | |
| LinkHub | Q9NRJ1. |
| ProtoNet | Search... |
Entry information
| Entry name | MOST1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NRJ1 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 8 Human chromosome 8: 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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