Entity Details

Primary name LINES_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NG48
EntryNameLINES_HUMAN
FullNameProtein Lines homolog 1
TaxID9606
Evidenceevidence at transcript level
Length757
SequenceStatuscomplete
DateCreated2008-02-05
DateModified2021-06-02

Ontological Relatives

GenesLINS1

GO terms

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GOName
GO:0050890 cognition

Subcellular Location

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Domains

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DomainNameCategoryType
IPR024875 Protein LinesFamilyFamily
IPR029415 Protein Lines, C-terminalDomainDomain
IPR032794 Protein Lines, N-terminalDomainDomain

Diseases

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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

1 interaction

InteractorPartnerSourcesPublicationsLink
LINES_HUMANCLK1_HUMANBioGRID26167880 details