Entity Details

Primary name LINS1
Entity type gene
Source Source Link

Details

PrimaryID55180
RefseqGeneNG_034076
SymbolLINS1
Namelines homolog 1
Chromosome15
Location15q26.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsLINES_HUMAN

GO terms

Show/Hide Table
GOName
GO:0050890 cognition

Diseases

Show/Hide Table
Disease IDSourceNameDescription
614340 OMIMMental 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

4 interactions

InteractorPartnerSourcesPublicationsLink
LINS1CLK1BioGRID26167880 details
LINS1PLRG1BioGRID, IntAct28514442 details
LINS1ELAVL1BioGRID19322201 details
LINS1APEX1BioGRID28986522 details