Reviewed,
UniProtKB/Swiss-Prot Q53TS8 (AL2SA_HUMAN)
Last modified
December 16, 2008.
Version 31.
History...
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Names and origin · Protein attributes · Ontologies · Alternative products · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 11 protein | ||
| 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 | 623 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
Ontologies
Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Polymorphism |
Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q53TS8-1) 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: Q53TS8-2) The sequence of this isoform differs from the canonical sequence as follows: 388-395: DIPLVNEE → GGFFTKRI 396-623: Missing. | ||||||
| Notes: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 623 | 623 | Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 11 protein | PRO_0000076174 | |||||
Natural variations | |||||||||
| Alternative sequence | 388 – 395 | 8 | DIPLVNEE → GGFFTKRI in isoform 2. | VSP_016788 | |||||
| Alternative sequence | 396 – 623 | 228 | Missing in isoform 2. | VSP_016789 | |||||
| Natural variant | 123 | 1 | K → M in a colorectal cancer sample; somatic mutation. Ref.4 | VAR_035787 | |||||
| Natural variant | 376 | 1 | H → Q: dbSNP rs10804117. Ref.1 Ref.3 | VAR_024769 | |||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| AK058080 mRNA. Translation: BAB71654.1. AC007282 Genomic DNA. Translation: AAY14693.1. BC030659 mRNA. Translation: AAH30659.1. | |
| RefSeq | NP_689738.3. |
| UniGene | Hs.335788 |
3D structure databases | |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q53TS8. 5 interactions. |
PTM databases | |
| PhosphoSite | Q53TS8. |
Proteomic databases | |
| PRIDE | Q53TS8. |
Genome annotation databases | |
| Ensembl | ENSG00000155754. Homo sapiens. [Contig view] |
| GeneID | 151254. |
| KEGG | hsa:151254. |
| NMPDR | fig|9606.3.peg.19160. |
Organism-specific databases | |
| GeneCards | GC02M202060. |
| HGNC | HGNC:14438. ALS2CR11. |
| PharmGKB | PA24734. |
| GenAtlas | Search... |
Phylogenomic databases | |
| HOGENOM | Q53TS8. |
| HOVERGEN | Q53TS8. |
Gene expression databases | |
| ArrayExpress | Q53TS8. |
| CleanEx | HS_ALS2CR11. |
| GermOnline | ENSG00000155754. Homo sapiens. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 86649. |
Entry information
| Entry name | AL2SA_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q53TS8 Secondary accession number(s): Q8NCN6, Q96LN4 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
Relevant documents
| Human chromosome 2 Human chromosome 2: 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 |

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