Entity Details
| Primary name |
TGDS_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | O95455 |
| EntryName | TGDS_HUMAN |
| FullName | dTDP-D-glucose 4,6-dehydratase |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 350 |
| SequenceStatus | complete |
| DateCreated | 2003-04-23 |
| DateModified | 2021-06-02 |
GO terms
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| GO | Name |
| GO:0008460 | dTDP-glucose 4,6-dehydratase activity |
| GO:0009225 | nucleotide-sugar metabolic process |
Subcellular Location
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Domains
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| Domain | Name | Category | Type |
| IPR005888 | dTDP-glucose 4,6-dehydratase | Family | Family |
| IPR016040 | NAD(P)-binding domain | Domain | Domain |
| IPR036291 | NAD(P)-binding domain superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 616145 | OMIM | Catel-Manzke syndrome (CATMANS) | A syndrome characterized by Pierre Robin sequence and a unique form of bilateral hyperphalangy causing a clinodactyly of the index finger. Pierre Robin sequence includes an opening in the roof of the mouth (a cleft palate), a large tongue (macroglossia), and a small lower jaw (micrognathia). The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions