Entity Details
| Primary name |
PIGC_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q92535 |
| EntryName | PIGC_HUMAN |
| FullName | Phosphatidylinositol N-acetylglucosaminyltransferase subunit C |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 297 |
| SequenceStatus | complete |
| DateCreated | 2001-07-11 |
| DateModified | 2021-06-02 |
GO terms
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| GO | Name |
| GO:0000506 | glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex |
| GO:0003824 | catalytic activity |
| GO:0005789 | endoplasmic reticulum membrane |
| GO:0006506 | GPI anchor biosynthetic process |
| GO:0016021 | integral component of membrane |
| GO:0016254 | preassembly of GPI anchor in ER membrane |
| GO:0017176 | phosphatidylinositol N-acetylglucosaminyltransferase activity |
Subcellular Location
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| Subcellular Location |
| Endoplasmic reticulum membrane |
Domains
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| Domain | Name | Category | Type |
| IPR009450 | Phosphatidylinositol N-acetylglucosaminyltransferase subunit C | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 617816 | OMIM | Glycosylphosphatidylinositol biosynthesis defect 16 (GPIBD16) | An autosomal recessive disorder characterized by delayed psychomotor development, intellectual disability, and seizures. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
4 interactions