Q52M58 (CN177_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 50.
History...
Names·Attributes·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Putative uncharacterized protein C14orf177 | ||
| 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 | 125 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 125 | 125 | Putative uncharacterized protein C14orf177 | PRO_0000274267 | |||||
Natural variations | |||||||||
| Natural variant | 3 | 1 | R → W. Ref.2 Corresponds to variant rs17097718 [ dbSNP | Ensembl ]. | VAR_030224 | |||||
| Natural variant | 33 | 1 | V → A. Corresponds to variant rs4905757 [ dbSNP | Ensembl ]. | VAR_030225 | |||||
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] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. Tissue: Testis. |
| [2] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT TRP-3. Tissue: Heart and Lung. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK098639 mRNA. Translation: BAC05361.1. BC093661 mRNA. Translation: AAH93661.1. |
| IPI | IPI00297704. |
| RefSeq | NP_872366.2. NM_182560.2. |
| UniGene | Hs.448754. |
3D structure databases | |
| ProteinModelPortal | Q52M58. |
| ModBase | Search... |
Proteomic databases | |
| PaxDb | Q52M58. |
| PRIDE | Q52M58. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000325812; ENSP00000321360; ENSG00000176605. |
| GeneID | 283598. |
| KEGG | hsa:283598. |
| UCSC | uc001yfz.2. human. |
Organism-specific databases | |
| CTD | 283598. |
| GeneCards | GC14P099177. |
| HGNC | HGNC:26375. C14orf177. |
| HPA | HPA018091. |
| neXtProt | NX_Q52M58. |
| PharmGKB | PA145149653. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG74493. |
| HOGENOM | HOG000111835. |
| InParanoid | Q52M58. |
| OMA | TISAFCA. |
| OrthoDB | EOG4VX26M. |
| PhylomeDB | Q52M58. |
Gene expression databases | |
| ArrayExpress | Q52M58. |
| Bgee | Q52M58. |
| CleanEx | HS_C14orf177. |
| Genevestigator | Q52M58. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 283598. |
| NextBio | 94084. |
Entry information
| Entry name | CN177_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q52M58 Secondary accession number(s): Q8N7D2 | ||||||||
| 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 14 Human chromosome 14: 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
