Entity Details

Primary name LMA2L_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H0V9
EntryNameLMA2L_HUMAN
FullNameVIP36-like protein
TaxID9606
Evidenceevidence at protein level
Length348
SequenceStatuscomplete
DateCreated2003-04-04
DateModified2021-06-02

Ontological Relatives

GenesLMAN2L

GO terms

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GOName
GO:0000139 Golgi membrane
GO:0005537 mannose binding
GO:0005789 endoplasmic reticulum membrane
GO:0005793 endoplasmic reticulum-Golgi intermediate compartment
GO:0005794 Golgi apparatus
GO:0006457 protein folding
GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport
GO:0007029 endoplasmic reticulum organization
GO:0007030 Golgi organization
GO:0015031 protein transport
GO:0016021 integral component of membrane
GO:0030134 COPII-coated ER to Golgi transport vesicle
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Endoplasmic reticulum membrane
Golgi apparatus membrane

Domains

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DomainNameCategoryType
IPR005052 Legume-like lectinDomainDomain
IPR013320 Concanavalin A-like lectin/glucanase domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
616887 OMIMMental retardation, autosomal recessive 52 (MRT52)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. MRT52 clinical features include global developmental delay, severe intellectual disability with poor speech, and mild seizures in early childhood. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
LMA2L_HUMANZDH17_HUMANBioGRID, IntAct24705354 details
LMA2L_HUMANMAL_HUMANBioGRID, IntAct32296183 details
LMA2L_HUMANHD_HUMANIntAct32814053 details