Q5T742 (CJ025_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 56.
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 C10orf25 | ||
| 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 | 122 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Secreted Potential. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Secreted |
| Coding sequence diversity | Polymorphism |
| Domain | Signal |
| PTM | Glycoprotein |
| Technical term | Complete proteome Reference 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 – 28 | 28 | Potential | ||||||
| Chain | 29 – 122 | 94 | Uncharacterized protein C10orf25 | PRO_0000019548 | |||||
Amino acid modifications | |||||||||
| Glycosylation | 49 | 1 | N-linked (GlcNAc...) Potential | ||||||
Natural variations | |||||||||
| Natural variant | 61 | 1 | P → L. Corresponds to variant rs41301609 [ dbSNP | Ensembl ]. | VAR_061603 | |||||
| Natural variant | 63 | 1 | I → N. Ref.1 Ref.3 Ref.4 Corresponds to variant rs12269028 [ dbSNP | Ensembl ]. | VAR_047102 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK055129 mRNA. Translation: BAB70858.1. AL353801 Genomic DNA. Translation: CAI13067.1. CH471160 Genomic DNA. Translation: EAW86630.1. BC130369 mRNA. Translation: AAI30370.1. BC130395 mRNA. Translation: AAI30396.1. |
| IPI | IPI00043749. |
| RefSeq | NP_001034469.2. NM_001039380.2. |
| UniGene | Hs.729435. |
3D structure databases | |
| ProteinModelPortal | Q5T742. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q5T742. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000298298; ENSP00000298298; ENSG00000165511. |
| GeneID | 220979. |
| KEGG | hsa:220979. |
| UCSC | uc001jbv.1. human. |
Organism-specific databases | |
| CTD | 220979. |
| GeneCards | GC10M045493. |
| HGNC | HGNC:23509. C10orf25. |
| neXtProt | NX_Q5T742. |
| PharmGKB | PA134916491. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | maNOG24184. |
| GeneTree | ENSGT00390000018615. |
| InParanoid | Q5T742. |
| OMA | KAPARWE. |
| OrthoDB | EOG402WTH. |
| PhylomeDB | Q5T742. |
Gene expression databases | |
| ArrayExpress | Q5T742. |
| Bgee | Q5T742. |
| Genevestigator | Q5T742. |
| GermOnline | ENSG00000165511. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| NextBio | 91128. |
Entry information
| Entry name | CJ025_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q5T742 Secondary accession number(s): A1L424, Q96NM5 | ||||||||
| 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 10 Human chromosome 10: 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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