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
Show/Hide Table
Domains
Show/Hide Table
Domain | Name | Category | Type |
IPR024875 | Protein Lines | Family | Family |
IPR029415 | Protein Lines, C-terminal | Domain | Domain |
IPR032794 | Protein Lines, N-terminal | Domain | Domain |
Diseases
Show/Hide Table
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