P59052 (CU088_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 56.
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 C21orf88 | ||
| 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 | 145 AA. |
| Sequence status | Complete. |
| Protein existence | Uncertain |
General annotation (Comments)
| Tissue specificity | Ubiquitous. |
| Caution | Product of a dubious CDS prediction. |
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: P59052-1) 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: P59052-2) The sequence of this isoform differs from the canonical sequence as follows: 52-64: GGQKSHGLCWLLC → NIQWHKRDQLGDN 65-145: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 145 | 145 | Putative uncharacterized protein C21orf88 | PRO_0000079538 | |||||
Natural variations | |||||||||
| Alternative sequence | 52 – 64 | 13 | GGQKS…CWLLC → NIQWHKRDQLGDN in isoform 2. | VSP_003836 | |||||
| Alternative sequence | 65 – 145 | 81 | Missing in isoform 2. | VSP_003837 | |||||
Experimental info | |||||||||
| Sequence conflict | 81 | 1 | C → W in AAM53522. Ref.1 | ||||||
| Sequence conflict | 81 | 1 | C → W in BC119737. Ref.4 | ||||||
| Sequence conflict | 81 | 1 | C → W in BC119738. Ref.4 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF426266 mRNA. Translation: AAM53522.1. AF426267 mRNA. Translation: AAM53523.1. AF064860 Genomic DNA. No translation available. CH471079 Genomic DNA. Translation: EAX09636.1. BC119737 mRNA. No translation available. BC119738 mRNA. No translation available. |
| IPI | IPI00168289. IPI00218783. |
| UniGene | Hs.375120. |
3D structure databases | |
| ProteinModelPortal | P59052. |
| ModBase | Search... |
Proteomic databases | |
| PRIDE | P59052. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000380612; ENSP00000369986; ENSG00000184809. |
Organism-specific databases | |
| GeneCards | GC21M040969. |
| HGNC | HGNC:16424. C21orf88. |
| HPA | HPA021156. |
| neXtProt | NX_P59052. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG21716. |
| GeneTree | ENSGT00390000018450. |
| InParanoid | P59052. |
| OMA | CWLLCFV. |
| OrthoDB | EOG4STS5V. |
Gene expression databases | |
| ArrayExpress | P59052. |
| Bgee | P59052. |
| CleanEx | HS_C21orf88. |
| Genevestigator | P59052. |
| GermOnline | ENSG00000184809. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Entry information
| Entry name | CU088_HUMAN | ||||||||
| Accession | Primary (citable) accession number: P59052 Secondary accession number(s): Q0VDC1, Q547X5 | ||||||||
| 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 |

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