Entity Details

Primary name SC23A_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15436
EntryNameSC23A_HUMAN
FullNameProtein transport protein Sec23A
TaxID9606
Evidenceevidence at protein level
Length765
SequenceStatuscomplete
DateCreated1997-11-01
DateModified2021-06-02

Ontological Relatives

GenesSEC23A

GO terms

Show/Hide Table
GOName
GO:0000139 Golgi membrane
GO:0002474 antigen processing and presentation of peptide antigen via MHC class I
GO:0005096 GTPase activator activity
GO:0005789 endoplasmic reticulum membrane
GO:0005829 cytosol
GO:0006886 intracellular protein transport
GO:0006888 endoplasmic reticulum to Golgi vesicle-mediated transport
GO:0008270 zinc ion binding
GO:0012507 ER to Golgi transport vesicle membrane
GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II
GO:0019898 extrinsic component of membrane
GO:0030127 COPII vesicle coat
GO:0048208 COPII vesicle coating
GO:0048471 perinuclear region of cytoplasm
GO:0070971 endoplasmic reticulum exit site
GO:0072659 protein localization to plasma membrane
GO:0090110 COPII-coated vesicle cargo loading

Subcellular Location

Show/Hide Table
Subcellular Location
Cytoplasm
Cytoplasmic vesicle
Endoplasmic reticulum membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR006895 Zinc finger, Sec23/Sec24-typeDomainDomain
IPR006896 Sec23/Sec24, trunk domainDomainDomain
IPR006900 Sec23/Sec24, helical domainDomainDomain
IPR007123 Gelsolin-like domainDomainDomain
IPR012990 Sec23/Sec24 beta-sandwichDomainDomain
IPR029006 ADF-H/Gelsolin-like domain superfamilyFamilyHomologous superfamily
IPR036174 Zinc finger, Sec23/Sec24-type superfamilyFamilyHomologous superfamily
IPR036175 Sec23/Sec24 helical domain superfamilyFamilyHomologous superfamily
IPR036180 Gelsolin-like domain superfamilyFamilyHomologous superfamily
IPR036465 von Willebrand factor A-like domain superfamilyFamilyHomologous superfamily
IPR037364 Protein transport protein Sec23FamilyFamily
IPR037550 Sec23, C-terminalDomainDomain

Diseases

Show/Hide Table
Disease IDSourceNameDescription
607812 OMIMCraniolenticulosutural dysplasia (CLSD)Autosomal recessive syndrome characterized by late-closing fontanels, sutural cataracts, facial dysmorphisms and skeletal defects. The disease is caused by variants affecting the gene represented in this entry.

Interactions

42 interactions

InteractorPartnerSourcesPublicationsLink
SC23A_HUMANSC24B_HUMANBioGRID, HPRD, IntAct10075675 22939629 26344197 details
SC23A_HUMANSC24C_HUMANBioGRID, HPRD, IntAct10075675 18692470 22939629 26344197 details
SC23A_HUMANCDK18_HUMANHPRD, IntAct16091426 details
SC23A_HUMANCDK16_HUMANHPRD, IntAct16091426 details
SC23A_HUMANSC24D_HUMANBioGRID, IntAct, MINT18843296 26344197 32296183 details
SC23A_HUMANGLRA2_HUMANBioGRID, IntAct21988832 details
SC23A_HUMANSDCB2_HUMANBioGRID, IntAct21988832 details
SC23A_HUMANTNFL6_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANDYN2_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANSF01_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANPIAS2_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANFATE1_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANSUCB1_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANMNAR1_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANWBP11_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANBNIP3_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANMFF_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANDTX2_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANERGI3_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANCXA8_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANRN19B_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANSL7A1_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANERLN1_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANCL17A_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANSC23B_HUMANBioGRID, IntAct26344197 32296183 details
SC23A_HUMANS23IP_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANTGO1_HUMANBioGRID, IntAct19269366 28442536 32296183 details
SC23A_HUMANTNF14_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANTM45B_HUMANBioGRID, IntAct32296183 details
SC23A_HUMANDCTN1_HUMANHPRD, IntAct15580264 32814053 details
SC23A_HUMANSC16A_HUMANBioGRID, HPRD17192411 26496610 details
SC23A_HUMANMIA2_HUMANBioGRID21525241 details
SC23A_HUMANCAPS1_HUMANBioGRID32296183 details
SC23A_HUMANHOMEZ_HUMANBioGRID32296183 details
SC23A_HUMANHLAB_HUMANIntAct17353931 details
SC23A_HUMANTMED2_HUMANUniProt9472029 details
SC23A_HUMANTMED7_HUMANUniProt9472029 details
SC23A_HUMANTMED3_HUMANUniProt9472029 details
SC23A_HUMANERD21_HUMANUniProt9472029 details
SC23A_HUMANGALT1_HUMANUniProt9472029 details
SC23A_HUMANATOH1_HUMANBioGRID27542412 details
SC23A_HUMANTNR6C_HUMANBioGRID29395067 details