| SEM1 |
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| Identifiers |
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| Aliases | SEM1, DSS1, ECD, SHFD1, SHSF1, Shfdg1, SHFM1, split hand/foot malformation (ectrodactyly) type 1 |
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| External IDs | OMIM: 601285; MGI: 109238; HomoloGene: 38165; GeneCards: SEM1; OMA:SEM1 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 6 (mouse) |
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| | Band | 6|6 A1 | Start | 6,557,294 bp |
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| End | 6,578,663 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| | Top expressed in | - mandibular prominence
- maxillary prominence
- endothelial cell of lymphatic vessel
- medullary collecting duct
- body of femur
- medial ganglionic eminence
- hair follicle
- primitive streak
- abdominal wall
- dermis
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| Wikidata |
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26S proteasome complex subunit DSS1 is a protein that in humans is encoded by the SHFM1 gene.