P59090 (CU090_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
April 3, 2013.
Version 55.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Putative uncharacterized protein C21orf90 | ||
| 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 | 65 AA. |
| Sequence status | Complete. |
| Protein existence | Uncertain |
General annotation (Comments)
| Tissue specificity | Widely expressed. Not expressed in liver and muscle. Ref.1 |
| Caution | Product of a dubious gene prediction. Encoded in intron of TSPEAR. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: P59090-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: P59090-2) The sequence of this isoform differs from the canonical sequence as follows: 15-37: FSGFLSNIRGPLAGEDGMGDTQL → GARLCSQDPLEARPLPPTSSFVR 38-65: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 65 | 65 | Putative uncharacterized protein C21orf90 | PRO_0000079540 | |||||
Natural variations | |||||||||
| Alternative sequence | 15 – 37 | 23 | FSGFL…GDTQL → GARLCSQDPLEARPLPPTSS FVR in isoform 2. | VSP_003838 | |||||
| Alternative sequence | 38 – 65 | 28 | Missing in isoform 2. | VSP_003839 | |||||
Sequences
References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF426269 mRNA. Translation: AAM53525.1. AF426270 mRNA. Translation: AAM53526.1. AP001066 Genomic DNA. No translation available. BC101650 mRNA. No translation available. BC101654 mRNA. No translation available. |
| IPI | IPI00171428. IPI00219882. |
| UniGene | Hs.592163. |
3D structure databases | |
| ProteinModelPortal | P59090. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000333592. |
Proteomic databases | |
| PRIDE | P59090. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000330490; ENSP00000333592; ENSG00000182912. ENST00000354333; ENSP00000346295; ENSG00000182912. |
Organism-specific databases | |
| GeneCards | GC21P045937. |
| HGNC | HGNC:16428. C21orf90. |
| neXtProt | NX_P59090. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG279263. |
| HOGENOM | HOG000112066. |
| InParanoid | P59090. |
| OMA | CALKFSG. |
| OrthoDB | EOG4VMFHN. |
| PhylomeDB | P59090. |
Gene expression databases | |
| Bgee | P59090. |
| CleanEx | HS_C21orf90. |
| Genevestigator | P59090. |
| GermOnline | ENSG00000182912. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Entry information
| Entry name | CU090_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P59090 Secondary accession number(s): Q3MIX8 | ||||||||
| 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 21 Human chromosome 21: entries, gene names and cross-references to MIM |

Clusters with
