Entity Details

Primary name GOSR2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO14653
EntryNameGOSR2_HUMAN
FullNameGolgi SNAP receptor complex member 2
TaxID9606
Evidenceevidence at protein level
Length212
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesGOSR2

GO terms

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GOName
GO:0000139 Golgi membrane
GO:0000149 SNARE binding
GO:0005484 SNAP receptor activity
GO:0005789 endoplasmic reticulum membrane
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0006623 protein targeting to vacuole
GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport
GO:0006891 intra-Golgi vesicle-mediated transport
GO:0006896 Golgi to vacuole transport
GO:0012507 ER to Golgi transport vesicle membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0031201 SNARE complex
GO:0031902 late endosome membrane
GO:0033116 endoplasmic reticulum-Golgi intermediate compartment membrane
GO:0036498 IRE1-mediated unfolded protein response
GO:0042147 retrograde transport, endosome to Golgi
GO:0048208 COPII vesicle coating
GO:0048280 vesicle fusion with Golgi apparatus

Subcellular Location

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Subcellular Location
Endoplasmic reticulum membrane
Golgi apparatus
Golgi apparatus membrane

Domains

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DomainNameCategoryType
IPR010989 SNAREFamilyHomologous superfamily
IPR027027 GOSR2/Membrin/Bos1FamilyFamily

Diseases

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Disease IDSourceNameDescription
614018 OMIMEpilepsy, progressive myoclonic 6 (EPM6)A form of progressive myoclonic epilepsy, a clinically and genetically heterogeneous group of disorders defined by the combination of action and reflex myoclonus, other types of epileptic seizures, and progressive neurodegeneration and neurocognitive impairment. EPM6 is an autosomal recessive form characterized by onset of ataxia in the first years of life, followed by action myoclonus and seizures later in childhood, and loss of independent ambulation in the second decade. Cognition is not usually affected, although mild memory difficulties may occur in the third decade. The disease is caused by variants affecting the gene represented in this entry.

Interactions

54 interactions

InteractorPartnerSourcesPublicationsLink
GOSR2_HUMANGOG8F_HUMANIntAct25416956 details
GOSR2_HUMANSTX6_HUMANBioGRID, IntAct25416956 26186194 28514442 details
GOSR2_HUMANGOG8D_HUMANIntAct25416956 details
GOSR2_HUMANSTX4_HUMANBioGRID, IntAct25416956 32296183 details
GOSR2_HUMANKASH5_HUMANBioGRID, IntAct25416956 32296183 details
GOSR2_HUMANSTX1A_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANSPAG4_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANT106A_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANTMC5A_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANSTX5_HUMANBioGRID, HPRD, IntAct11035026 11927603 32296183 9094723 9647643 details
GOSR2_HUMANMF14B_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANF174A_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANTM205_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANAQP6_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANCYBR1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANEBP_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANLIME1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANGPR42_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANRIC3_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANMFSD5_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANJAGN1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANLEUTX_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANF209A_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANRN19B_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANIR3IP_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANEMC5_HUMANBioGRID, IntAct27342126 32296183 details
GOSR2_HUMANTLCD4_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANNTCP_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANT4S19_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANGP152_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANCR3L1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANAR13B_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANELOV4_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMAN3HIDH_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANCY561_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANMARH8_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANFATE1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANMFF_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANBET1_HUMANBioGRID, IntAct29568061 32296183 details
GOSR2_HUMANPELI1_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANRETR3_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANT106C_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANSOAT_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANBLCAP_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANNACHO_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANDHB13_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANGPX8_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANELOV5_HUMANBioGRID, IntAct32296183 details
GOSR2_HUMANUSO1_HUMANBioGRID, HPRD10903204 11927603 details
GOSR2_HUMANA4_HUMANBioGRID21832049 details
GOSR2_HUMANLMNA_HUMANBioGRID24623722 details
GOSR2_HUMANSNAA_HUMANBioGRID, HPRD, IntAct30833792 9349823 details
GOSR2_HUMANST7_HUMANBioGRID29395067 details
GOSR2_HUMANARF1_HUMANHPRD15781476 details