Unreviewed,
UniProtKB/TrEMBL Q52MC1 (Q52MC1_HUMAN)
Last modified
January 19, 2010.
Version 21.
History...
Clusters with 100%,
90%,
50% identity |
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Names and origin · Protein attributes · Sequences · References · Cross-references · Entry information
Names and origin
| Protein names | Submitted name: Cytotoxic T lymphocyte associated antigen 4 short spliced form EMBL AAY00166.1 |
| Organism | Homo sapiens (Human) EMBL AAY00166.1 |
| Taxonomic identifier | 9606 [NCBI] |
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 58 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level. |
Sequences
References
| [1] | "Identification of CTLA-4 isoforms produced by alternative splicing and their association with myasthenia gravis." Gu M., Kakoulidou M., Giscombe R., Pirskanen R., Lefvert A.K., Klareskog L., Wang X. Clin. Immunol. 128:374-381(2008) [PubMed: 18595775] [Abstract] Cited for: NUCLEOTIDE SEQUENCE. |
| [2] | "Human short spliced CD152 regulates gene transcription." Wang X.X., Gu M.M., Lefvert A.A. Submitted (APR-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AY999702 mRNA. Translation: AAY00166.1. |
| IPI | IPI00604432. |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | Q52MC1. |
Genome annotation databases | |
| Ensembl | ENST00000374470; ENSP00000363594; ENSG00000163599; Homo sapiens. [Genome view] |
Organism-specific databases | |
| HGNC | HGNC:2505. CTLA4. |
Phylogenomic databases | |
| HOVERGEN | Q52MC1. |
Gene expression databases | |
| ArrayExpress | Q52MC1. |
| Bgee | Q52MC1. |
Family and domain databases | |
| ProtoNet | Search... |
Entry information
| Entry name | Q52MC1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q52MC1 | ||||||||
| Entry history |
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| Entry status | Unreviewed (UniProtKB/TrEMBL) | ||||||||
| 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. | ||||||||

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