Reviewed,
UniProtKB/Swiss-Prot Q6GMV1 (ALG1L_HUMAN)
Last modified
November 24, 2009.
Version 39.
History...
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Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Sequence annotation (Features) · Sequences · References · Cross-references · Entry information · Relevant documents
Names and origin
| Protein names | Recommended name: Putative glycosyltransferase ALG1-like EC=2.4.1.- | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Complete 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 | 187 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is not processed. |
| Protein existence | Evidence at transcript level. |
General annotation (Comments)
| Function | Putative glycosyltransferase By similarity. |
| Sequence similarities | Belongs to the glycosyltransferase 1 family. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Molecular function | Glycosyltransferase Transferase |
| Technical term | Complete proteome |
| Gene Ontology (GO) | |
| Molecular function | transferase activity, transferring glycosyl groups Inferred from electronic annotation. Source: UniProtKB-KW |
| Complete GO annotation... | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 187 | 187 | Putative glycosyltransferase ALG1-like | PRO_0000326037 | |||||
Natural variations | |||||||||
| Natural variant | 135 | 1 | N → D: dbSNP rs3828357. | VAR_039962 | |||||
| Natural variant | 159 | 1 | I → T: dbSNP rs3811679. | VAR_039963 | |||||
| Natural variant | 184 | 1 | G → S: dbSNP rs3187686. | VAR_039964 | |||||
Sequences
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References
| [1] | "The DNA sequence, annotation and analysis of human chromosome 3." Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J. Gibbs R.A.Nature 440:1194-1198(2006) [PubMed: 16641997] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [2] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT ASP-135. Tissue: Brain. |
Cross-references
Sequence databases | |
|---|---|
| BC073816 mRNA. Translation: AAH73816.1. | |
| IPI | IPI00145612. |
| RefSeq | NP_001015050.1. |
| UniGene | Hs.591299 |
3D structure databases | |
| ModBase | Search... |
Protein family/group databases | |
| CAZy | GT33. Glycosyltransferase Family 33. |
Proteomic databases | |
| PRIDE | Q6GMV1. |
Genome annotation databases | |
| Ensembl | ENST00000340333; ENSP00000340009; ENSG00000189366; Homo sapiens. [Genome view] ENST00000437882; ENSP00000408369; ENSG00000189366; Homo sapiens. [Genome view] |
| GeneID | 200810. |
| KEGG | hsa:200810. |
| UCSC | uc003eig.1. human. |
Organism-specific databases | |
| CTD | 200810. |
| GeneCards | GC03M127130. GC11P067271. |
| HGNC | HGNC:33721. ALG1L. |
| GenAtlas | Search... |
Gene expression databases | |
| Genevestigator | Q6GMV1. |
Family and domain databases | |
| ProtoNet | Search... |
Other Resources | |
| NextBio | 89978. |
Entry information
| Entry name | ALG1L_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q6GMV1 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation project | HPI (Human Proteome Initiative) | ||||||||
| 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 3 Human chromosome 3: 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 |
| SIMILARITY comments Index of protein domains and families |

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