Entity Details

Primary name AP1B1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ10567
EntryNameAP1B1_HUMAN
FullNameAP-1 complex subunit beta-1
TaxID9606
Evidenceevidence at protein level
Length949
SequenceStatuscomplete
DateCreated1996-10-01
DateModified2021-06-02

Ontological Relatives

GenesAP1B1

GO terms

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GOName
GO:0000139 Golgi membrane
GO:0001822 kidney development
GO:0005765 lysosomal membrane
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0006886 intracellular protein transport
GO:0006892 post-Golgi vesicle-mediated transport
GO:0007368 determination of left/right symmetry
GO:0007507 heart development
GO:0016192 vesicle-mediated transport
GO:0019886 antigen processing and presentation of exogenous peptide antigen via MHC class II
GO:0019901 protein kinase binding
GO:0030131 clathrin adaptor complex
GO:0030276 clathrin binding
GO:0030659 cytoplasmic vesicle membrane
GO:0030665 clathrin-coated vesicle membrane
GO:0032588 trans-Golgi network membrane
GO:0043231 intracellular membrane-bounded organelle
GO:0050690 regulation of defense response to virus by virus

Subcellular Location

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Subcellular Location
Cytoplasmic vesicle
Golgi apparatus

Domains

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DomainNameCategoryType
IPR000225 ArmadilloRepeatRepeat
IPR002553 Clathrin/coatomer adaptor, adaptin-like, N-terminalDomainDomain
IPR008152 Clathrin adaptor, alpha/beta/gamma-adaptin, appendage, Ig-like subdomainDomainDomain
IPR009028 Coatomer/calthrin adaptor appendage, C-terminal subdomainFamilyHomologous superfamily
IPR011989 Armadillo-like helicalFamilyHomologous superfamily
IPR012295 TBP domain superfamilyFamilyHomologous superfamily
IPR013037 Clathrin adaptor, beta-adaptin, appendage, Ig-like subdomainFamilyHomologous superfamily
IPR013041 Clathrin adaptor, appendage, Ig-like subdomain superfamilyFamilyHomologous superfamily
IPR015151 Beta-adaptin appendage, C-terminal subdomainDomainDomain
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR016342 AP-1/2/4 complex subunit betaFamilyFamily
IPR026739 AP complex subunit betaFamilyFamily

Diseases

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Disease IDSourceNameDescription
242150 OMIMKeratitis-ichthyosis-deafness syndrome, autosomal recessive (KIDAR)An autosomal recessive form of keratitis-ichthyosis-deafness syndrome, a disease characterized by the association of hyperkeratotic skin lesions with vascularizing keratitis and profound sensorineural hearing loss. KIDAR patients manifest ichthyosis, failure to thrive and developmental delay in childhood, thrombocytopenia, photophobia, and progressive hearing loss. Low plasma copper and ceruloplasmin levels have been reported in some patients. The disease is caused by variants affecting the gene represented in this entry.

Interactions

55 interactions

InteractorPartnerSourcesPublicationsLink
AP1B1_HUMANNTRK2_HUMANBioGRID, IntAct21988832 details
AP1B1_HUMANARF1_HUMANBioGRID, HPRD, IntAct11926829 23415225 details
AP1B1_HUMANAP1G1_HUMANBioGRID, HPRD, IntAct10535737 10747088 11409905 22939629 23415225 26344197 7593184 9733768 details
AP1B1_HUMANAP2M1_HUMANBioGRID, IntAct19380743 24189400 26186194 26344197 28514442 7593184 details
AP1B1_HUMANMTR1B_HUMANBioGRID, IntAct26514267 details
AP1B1_HUMANKI13A_HUMANBioGRID, HPRD, IntAct11106728 32296183 details
AP1B1_HUMANPS1C2_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANARH_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANFND11_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANMYG1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANMSGN1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANTB22B_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANNUP54_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANU2AF5_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANMLH1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANT10IP_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANGPAN1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANCRBB1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANGTF2I_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANSYFM_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANRNF39_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANNECP1_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANP121A_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANAGR3_HUMANBioGRID, IntAct32296183 details
AP1B1_HUMANEPN4_HUMANBioGRID, IntAct12429846 12538641 28514442 details
AP1B1_HUMANAMPH_HUMANBioGRID, IntAct28514442 9280305 details
AP1B1_HUMANPRKDC_HUMANBioGRID10608806 details
AP1B1_HUMANATM_HUMANBioGRID, HPRD10608806 9707615 details
AP1B1_HUMANATR_HUMANBioGRID10608806 details
AP1B1_HUMANCLH1_HUMANBioGRID, HPRD11451993 9280305 details
AP1B1_HUMANAP1M1_HUMANBioGRID22939629 26344197 7593184 details
AP1B1_HUMANSHBG_HUMANBioGRID, HPRD15862967 details
AP1B1_HUMANBARD1_HUMANBioGRID22990118 details
AP1B1_HUMANARRB2_HUMANBioGRID, HPRD10097102 11877451 12070169 details
AP1B1_HUMANGTR8_HUMANBioGRID16723738 details
AP1B1_HUMANFMNL2_HUMANBioGRID32296183 details
AP1B1_HUMANU2AF1_HUMANBioGRID32296183 details
AP1B1_HUMANAP1G2_HUMANBioGRID32296183 details
AP1B1_HUMANAP1B1_HUMANHPRD9733768 details
AP1B1_HUMANBUB1B_HUMANHPRD12419313 details
AP1B1_HUMANBUB1_HUMANHPRD12419313 details
AP1B1_HUMANCBP_HUMANHPRD15752756 details
AP1B1_HUMANSMAD2_HUMANHPRD15231748 details
AP1B1_HUMANMCAF1_HUMANHPRD15231748 details
AP1B1_HUMANEPS15_HUMANBioGRID, IntAct12538641 19380743 details
AP1B1_HUMANAP1M2_HUMANBioGRID, HPRD, IntAct10535737 26186194 26344197 28514442 details
AP1B1_HUMANCABIN_HUMANBioGRID10931822 details
AP1B1_HUMANSYUA_HUMANBioGRID18614564 details
AP1B1_HUMANEPN1_HUMANBioGRID12538641 details
AP1B1_HUMANAP180_HUMANBioGRID12538641 details
AP1B1_HUMANSMAP2_HUMANBioGRID29395067 details
AP1B1_HUMANTTP_HUMANBioGRID29395067 details
AP1B1_HUMANARF6_HUMANBioGRID, HPRD11926829 34079125 details
AP1B1_HUMANPI51C_HUMANHPRD17290217 details
AP1B1_HUMANARF5_HUMANHPRD11926829 details