Entity Details
| Primary name |
LINES_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q8NG48 |
| EntryName | LINES_HUMAN |
| FullName | Protein Lines homolog 1 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 757 |
| SequenceStatus | complete |
| DateCreated | 2008-02-05 |
| DateModified | 2021-06-02 |
Subcellular Location
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Domains
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| Domain | Name | Category | Type |
| IPR024875 | Protein Lines | Family | Family |
| IPR029415 | Protein Lines, C-terminal | Domain | Domain |
| IPR032794 | Protein Lines, N-terminal | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 614340 | OMIM | Mental retardation, autosomal recessive 27 (MRT27) | A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction