Q9NUD7 (CT096_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 75.
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 C20orf96 | ||
| 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 | 363 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Sequence caution | The sequence BAC03772.1 differs from that shown. Reason: Frameshift at position 304. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Domain | Coiled coil |
| 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 – 363 | 363 | Uncharacterized protein C20orf96 | PRO_0000079450 | |||||
Regions | |||||||||
| Coiled coil | 109 – 329 | 221 | Potential | ||||||
| Compositional bias | 264 – 268 | 5 | Poly-Lys | ||||||
Natural variations | |||||||||
| Natural variant | 305 | 1 | I → F. Ref.1 Ref.3 Ref.4 Corresponds to variant rs3827147 [ dbSNP | Ensembl ]. | VAR_056847 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK097394 mRNA. Translation: BAC05033.1. AK091924 mRNA. Translation: BAC03772.1. Frameshift. AL034548 Genomic DNA. Translation: CAB81629.2. CH471133 Genomic DNA. Translation: EAX10681.1. BC134417 mRNA. Translation: AAI34418.1. BC137450 mRNA. Translation: AAI37451.1. |
| IPI | IPI00300683. |
| RefSeq | NP_542138.1. NM_080571.1. NP_695001.2. NM_153269.2. |
| UniGene | Hs.348112. |
3D structure databases | |
| ProteinModelPortal | Q9NUD7. |
| ModBase | Search... |
PTM databases | |
| PhosphoSite | Q9NUD7. |
Polymorphism databases | |
| DMDM | 26392576. |
Proteomic databases | |
| PaxDb | Q9NUD7. |
| PRIDE | Q9NUD7. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000360321; ENSP00000353470; ENSG00000196476. |
| GeneID | 140680. |
| KEGG | hsa:140680. |
| UCSC | uc002wde.2. human. |
Organism-specific databases | |
| CTD | 140680. |
| GeneCards | GC20M000246. |
| HGNC | HGNC:16227. C20orf96. |
| HPA | HPA048649. |
| neXtProt | NX_Q9NUD7. |
| PharmGKB | PA25803. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG25990. |
| HOGENOM | HOG000112025. |
| HOVERGEN | HBG051181. |
| InParanoid | Q9NUD7. |
| OMA | REVIFED. |
| OrthoDB | EOG4FTW1H. |
| PhylomeDB | Q9NUD7. |
Gene expression databases | |
| ArrayExpress | Q9NUD7. |
| Bgee | Q9NUD7. |
| CleanEx | HS_C20orf96. |
| Genevestigator | Q9NUD7. |
| GermOnline | ENSG00000196476. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| ChiTaRS | C20orf96. human. |
| GenomeRNAi | 140680. |
| NextBio | 84213. |
Entry information
| Entry name | CT096_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9NUD7 Secondary accession number(s): A3KPE0 Q8NAX5 | ||||||||
| Entry history |
| ||||||||
| 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 20 Human chromosome 20: 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
