alg2 | GeneID:2539854 | Schizosaccharomyces pombe
Gene Summary
[
] NCBI Entrez Gene
| Gene ID | 2539854 | Official Symbol | alg2 |
|---|---|---|---|
| Locus | SPBC11B10.01 | Gene Type | protein-coding |
| Synonyms | SPBC32H8.14 | ||
| Full Name | N/A | ||
| Description | mannosyltransferase complex subunit Alg2 | ||
| Chromosome | N/A | ||
| Also Known As | |||
| Summary | N/A | ||
Orthologs and Paralogs
[
] Homologs - NCBI's HomoloGene Group: 5930
| ID | Symbol | Protein | Species |
|---|---|---|---|
| GeneID:38374 | CG1291 | NP_647772.1 | Drosophila melanogaster |
| GeneID:56737 | Alg2 | NP_064382.2 | Mus musculus |
| GeneID:85365 | ALG2 | NP_149078.1 | Homo sapiens |
| GeneID:173912 | F09E5.2 | NP_495010.2 | Caenorhabditis elegans |
| GeneID:313231 | Alg2 | XP_232987.3 | Rattus norvegicus |
| GeneID:403068 | alg2 | NP_001098406.1 | Danio rerio |
| GeneID:472993 | ALG2 | XP_528363.2 | Pan troglodytes |
| GeneID:474780 | ALG2 | XP_532010.2 | Canis lupus familiaris |
| GeneID:538899 | ALG2 | XP_583521.1 | Bos taurus |
| GeneID:844216 | AT1G78800 | NP_178001.2 | Arabidopsis thaliana |
| GeneID:852815 | ALG2 | NP_011450.1 | Saccharomyces cerevisiae |
| GeneID:1281939 | AgaP_AGAP001232 | XP_321925.2 | Anopheles gambiae |
| GeneID:2539854 | alg2 | NP_595621.2 | Schizosaccharomyces pombe |
| GeneID:2681481 | MGG_02384 | XP_365682.2 | Magnaporthe grisea |
| GeneID:2704609 | NCU03503.1 | XP_322761.1 | Neurospora crassa |
| GeneID:2896861 | KLLA0B02420g | XP_451639.1 | Kluyveromyces lactis |
| GeneID:4336813 | Os04g0589600 | NP_001053699.1 | Oryza sativa |
| GeneID:4621679 | AGOS_AFL098W | NP_985452.1 | Eremothecium gossypii |
Gene Classification
[
] Gene Ontology
| ID | Category | GO Term |
|---|---|---|
| GO:0005783 | Component | endoplasmic reticulum |
| GO:0016021 | Component | integral to membrane |
| GO:0004378 | Function | glycolipid 3-alpha-mannosyltransferase activity |
| GO:0033164 | Function | glycolipid 6-alpha-mannosyltransferase activity |
| GO:0004376 | Function | glycolipid mannosyltransferase activity |
| GO:0043413 | Process | biopolymer glycosylation |
| GO:0006490 | Process | oligosaccharide-lipid intermediate assembly |
RefSeq Isoforms
[
] RefSeq Annotation and UniProt Database
| No. | RefSeq RNA | RefSeq Protein | UniProt Equivalent |
|---|---|---|---|
| 1 | NM_001021515 | NP_595621 | |
Selected Publications
[
] Gene-related publications indexed at PubMed
- [
] Aslett M, et al. (2006) "Gene Ontology annotation status of the fission yeast genome: preliminary coverage approaches 100%." Yeast. 23(13):913-919. PMID:17072883 - [
] Wood V, et al. (2002) "The genome sequence of Schizosaccharomyces pombe." Nature. 415(6874):871-880. PMID:11859360
In this review, we present an overview of the Gene Ontology (GO) structure and describe how the GO is implemented for Sz. pombe and made available via Sz. pombe GeneDB (http://www.genedb.org/genedb/pombe/). We give a detailed progress report of Sz. pombe GO annotation, providing the current status of both manual and automatic annotations. Fission yeast has at least one GO annotation for 98.3% of its genes (excluding annotations to 'unknown' terms), greater than the current percentage coverage for any other organism. Approximately 65% (3225 gene products) have at least one annotation to each of the three ontologies (biological process, cellular component and molecular function). Approximately 30% (1443 gene products) have GO terms derived directly from small-scale experiments in fission yeast, supporting the validity of fission yeast as a model eukaryote and a reference organism.
We have sequenced and annotated the genome of fission yeast (Schizosaccharomyces pombe), which contains the smallest number of protein-coding genes yet recorded for a eukaryote: 4,824. The centromeres are between 35 and 110 kilobases (kb) and contain related repeats including a highly conserved 1.8-kb element. Regions upstream of genes are longer than in budding yeast (Saccharomyces cerevisiae), possibly reflecting more-extended control regions. Some 43% of the genes contain introns, of which there are 4,730. Fifty genes have significant similarity with human disease genes; half of these are cancer related. We identify highly conserved genes important for eukaryotic cell organization including those required for the cytoskeleton, compartmentation, cell-cycle control, proteolysis, protein phosphorylation and RNA splicing. These genes may have originated with the appearance of eukaryotic life. Few similarly conserved genes that are important for multicellular organization were identified, suggesting that the transition from prokaryotes to eukaryotes required more new genes than did the transition from unicellular to multicellular organization.