Entity Details
| Primary name |
TR19L_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q969Z4 |
| EntryName | TR19L_HUMAN |
| FullName | Tumor necrosis factor receptor superfamily member 19L |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 430 |
| SequenceStatus | complete |
| DateCreated | 2002-05-27 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
| Cytoplasm |
Domains
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| Domain | Name | Category | Type |
| IPR022248 | TNF receptor family, RELT | Family | Family |
| IPR022333 | Tumour necrosis factor receptor 19-like | Family | Family |
| IPR034048 | Tumor necrosis factor receptor 19-like, N-terminal | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 618386 | OMIM | Amelogenesis imperfecta 3C (AI3C) | An autosomal recessive form of amelogenesis imperfecta, a defect of enamel formation. AI3C is characterized by generalized enamel hypocalcification affecting primary and secondary dentition. The surface of the enamel is rough and often stained. After eruption, the occlusal enamel on the molars disappears due to attrition, leaving a ring of intact enamel remaining on the sides. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
4 interactions