| Gene: | | AMBN ( Homo sapiens ) | | ameloblastin (enamel matrix protein) |
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| Description: | Ameloblastin is thought to represent an unique ameloblast-specific gene product that may be important in enamel matrix formation and mineralization. The gene is located on chromosome 4 near other genes associated with mineralized tissues: osteopontin, bone sialoprotein, and bone morphogenetic protein 3. Based on its cytogenetic location, this gene is a candidate gene for one form of the disorder, dentinogenesis imperfecta, and/or the disorder, autosomal dominant amylogenesis imperfecta. [provided by RefSeq] |
| Synonyms: | ameloblastin; |
| Gene Type: | protein-coding |
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| Additional Data |
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| Homologs |
| Mus musculus: Ambn See the Mouse gene in context in: UCSC NCBI MapViewer |
| Rattus norvegicus: Ambn See the Rat gene in context in: UCSC NCBI MapViewer |
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| Rattus norvegicus | Ambn | genome assembly 3.1 | 14 | 21183341 - 21196650 | | | | Rat Celera Assembly | 14 | 18940132 - 18975936 | | | | RGSC genome assembly v3.4 | 14 | 21183338 - 21196650 | | | | Cytogenetic | 14 | p21 | | Mus musculus | Ambn | Mouse genome assembly build 36.1 | 5 | 88885036 - 88897556 | | | | Cytogenetic | 5 | 5 E1 | | Homo sapiens | AMBN | human genome assembly | 4 | 71638760 - 71653762 | | | | Human genome assembly build 36.2 | 4 | 71492590 - 71507594 | | | | Cytogenetic | 4 | q21 | | | | View comparative maps: | NCBI MapViewer | |
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Annotation |
| Molecular Function | |
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| Cellular Component | |
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External Links |
| Databases | | DATABASE | ID | SOURCE | | OMIM: | 601259 | ENTREZGENE | | HGNC ID: | AMBN | ENTREZGENE | | Entrez Gene: | AMBN | ENTREZGENE | | KEGG Report: | hsa:258 | ENTREZGENE | | HomoloGene Group ID: | 7625 | ENTREZGENE | | HPRD ID: | 03160 | ENTREZGENE |
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| Sequences | |
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References |
| Curated References |
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Database Information |
| RGD ID | 736409 |
| History | No Nomenclature events are recorded for this object |