Entity Details
| Primary name |
IGSF3_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | O75054 |
| EntryName | IGSF3_HUMAN |
| FullName | Immunoglobulin superfamily member 3 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 1194 |
| SequenceStatus | complete |
| DateCreated | 2008-02-26 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR003598 | Immunoglobulin subtype 2 | Domain | Domain |
| IPR003599 | Immunoglobulin subtype | Domain | Domain |
| IPR007110 | Immunoglobulin-like domain | Domain | Domain |
| IPR013106 | Immunoglobulin V-set domain | Domain | Domain |
| IPR013783 | Immunoglobulin-like fold | Family | Homologous superfamily |
| IPR036179 | Immunoglobulin-like domain superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 149700 | OMIM | Lacrimal duct defect (LCDD) | A condition resulting in the imbalance between tear production and tear drainage. Infants typically manifest persistent epiphora and/or recurrent infections of the lacrimal pathway, such as conjunctivitis. LCDD is caused by failure of the nasolacrimal duct to open into the inferior meatus. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions