AP2B1 - adaptor related protein complex 2 subunit beta 1 Gene

Also Known as ADTB2; AP105B; CLAPB1; AP2-BETA

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 163

About AP2B1

Cytogenetic location: 17q12 Genomic coordinates (GRCh38): 17:35,587,322-35,726,413 (from NCBI)

This gene has 22 transcripts (splice variants), 211 orthologues and 4 paralogues. Ubiquitous expression in brain (RPKM 64.4), testis (RPKM 50.1) and 25 other tissues.

Summary

The protein encoded by this gene is one of two large chain components of the assembly protein complex 2, which serves to link clathrin to receptors in coated vesicles. The encoded protein is found on the cytoplasmic face of coated vesicles in the plasma membrane. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

AP2B1 Products (2)

mRNA Protein Name
NM_001030006.2 NP_001025177.1 AP-2 complex subunit beta isoform a
NM_001282.3 NP_001273.1 AP-2 complex subunit beta isoform b

AP2B1 Protein Structure

Adaptin_N

Adaptin_N: Adaptin N terminal region (15 - 532)

Alpha_adaptinC2

Alpha_adaptinC2: Adaptin C-terminal domain (727 - 826)

B2-adapt-app_C

B2-adapt-app_C: Beta2-adaptin appendage, C-terminal sub-domain (840 - 950)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 951 a.a.
Protein Preferred Names Protein Names

AP-2 complex subunit beta

  • adapter-related protein complex 2 beta subunit

AP2B1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7-2 25416956
Intra
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7-2 25416956
Intra
AP2B1 P63010 XRCC6BP1 Homo sapiens Q8N4L5 25416956
Intra
AP2B1 P63010 TXN2 Homo sapiens Q99757 25416956
Intra
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 16189514
Intra
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 35271311
Intra
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 33961781
Intra
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
Intra
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
Intra
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
Intra
AP2B1 P63010 SLC25A6 Homo sapiens P12236 29892012
Intra
AP2B1 P63010 SLC25A6 Homo sapiens P12236 25416956
Intra
AP2B1 P63010 SLC25A6 Homo sapiens P12236 25416956
Intra
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7 25416956
Intra
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7 25416956
Intra
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5
Y2H
9341158
Intra
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5 16189514
Intra
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5 33961781
Intra
AP2B1 P63010 ITSN1 Homo sapiens Q15811 33961781
Intra
AP2B1 P63010 ITSN1 Homo sapiens Q15811 35044719
Intra
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
Intra
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
Intra
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
Intra
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 16189514
Intra
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 25416956
Intra
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 25416956
Intra
AP2B1 P63010 NECAP2 Homo sapiens Q9NVZ3 16189514
Intra
AP2B1 P63010 NECAP2 Homo sapiens Q9NVZ3 33961781
Intra
AP2B1 P63010 MEA1 Homo sapiens Q16626 33961781
Intra
AP2B1 P63010 MEA1 Homo sapiens Q16626 16189514
Intra
AP2B1 P63010 MEA1 Homo sapiens Q16626 16189514
Intra
AP2B1 P63010 LDLRAP1 Homo sapiens Q5SW96 16189514
Intra
AP2B1 P63010 LDLRAP1 Homo sapiens Q5SW96 25416956
Intra
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 25416956
Intra
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 25416956
Intra
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 33961781
Intra
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 16189514
Cross
AP2B1 P63010 Necap1 Mus musculus Q9CR95
NMR
24130457
Cross
AP2B1 P63010 Necap1 Mus musculus Q9CR95 24130457
Cross
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092 20603002
Cross
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092
Y2H
9341158
Cross
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092 25061211
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Cerebellar Degeneration
Char Syndrome
  • Patent Ductus Arteriosus With Facial Dysmorphism And Abnormal Fifth Digits

  • CHAR

Ataxia-Telangiectasia
  • Ataxia Telangiectasia

  • Louis-Bar Syndrome

  • AT

  • At1

  • Ataxia-Telangiectasia Syndrome

  • Ataxia - Telangiectasia Variant

  • Boder-Sedgwick Syndrome

  • Louis Bar Syndrome

  • Cerebello-Oculocutaneous Telangiectasia

  • Immunodeficiency With Ataxia Telangiectasia

  • A-T

  • Ataxia Telangiectasia Syndrome

  • Atm

  • Telangiectasia, Cerebello-Oculocutaneous

  • Ataxia-Telangiectasia Variant

Hypocalciuric Hypercalcemia, Familial, Type Iii
  • HHC3

  • Familial Hypocalciuric Hypercalcemia 3

  • Fbh3

  • Familial Hypocalciuric Hypercalcemia Type 3

  • Hypercalcemia, Familial Benign, Oklahoma Type

  • Hypocalciuric Hypercalcemia, Type Iii

  • Fhh Type 3

  • Hypocalciuric Hypercalcemia Type Iii

  • Familial Benign Hypercalcemia, Type Iii

  • Hypercalcemia, Familial Benign, Type Iii

  • Fbhok

  • Familial Benign Hypercalcemia, Oklahoma Variant

  • Familial Benign Hypercalcemia, Type 3

  • Hypercalcemia, Familial Benign, Type 3

  • Hypocalciuric Hypercalcemia, Familial, Type 3

  • Hypocalciuric Hypercalcemia, Familial 3

  • Familial Benign Hypercalcemia 3

  • Familial Benign Hypercalcemia Oklahoma Type

  • Familial Benign Hypocalciuric Hypercalcemia 3

  • Fbhh3

  • Fhh3

Branchiooculofacial Syndrome
  • Branchio-Oculo-Facial Syndrome

  • BOFS

  • Bof Syndrome

  • Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome

  • Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome

  • Branchial Clefts With Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, And Premature Aging

  • Branchial Clefts With Characteristic Facies Growth Retardation Imperforate Nasolacrimal Duct And Premature Aging

  • Bofs Syndrome

  • Lip Pseudocleft-Hemagiomatous Branchial Cyst Syndrome

Hypercholesterolemia, Familial, 4
  • Hypercholesterolemia, Autosomal Recessive

  • Arh

  • FHCL4

  • Autosomal Recessive Hypercholesterolemia

  • Arh1

  • Arh2

  • Autosomal Recessive Hypercholesterolemia 1

  • Autosomal Recessive Hypercholesterolemia 2

  • Fhcb1

  • Fhcb2

  • Hypercholesterolemia, Autosomal Recessive, 1, Formerly

  • Arh1, Formerly

  • Fhcb1, Formerly

  • Hypercholesterolemia, Autosomal Recessive, 2, Formerly

  • Arh2, Formerly

  • Fhcb2, Formerly

  • Familial Autosomal Recessive Hypercholesterolemia

  • Hypercholesterolemia, Familial, Autosomal Recessive

  • Hypercholesterolemia, Familial, Type 4

Patent Ductus Arteriosus 1
  • Patent Ductus Arteriosus

  • PDA1

  • Pda

  • Ductus Arteriosus, Patent

  • Patent Ductus Arteriosus, Susceptibility To

  • Patent Ductus Botalli

  • Patency Of The Ductus Arteriosus

  • Patent Ductus Arteriosus Familial

  • Ductus Arteriosus Patent

  • Patent Ductus Arteriosus - Persisting Type

Rhabdomyosarcoma
Mitochondrial Complex Iv Deficiency, Nuclear Type 1
  • Cytochrome C Oxidase Deficiency

  • Mitochondrial Complex Iv Deficiency

  • Cox Deficiency

  • Cytochrome-C Oxidase Deficiency Disease

  • MC1DN4

  • Cytochrome-C Oxidase Deficiency

  • MC4DN1

  • Mitochondrial Complex I Deficiency, Nuclear Type 4

  • Complex 4 Mitochondrial Respiratory Chain Deficiency

  • Complex Iv Deficiency

  • Mitochondrial Complex 1 Deficiency, Nuclear Type 4

  • Nuclear Type Mitochondrial Complex I Deficiency 4

  • Deficiency Of Mitochondrial Respiratory Chain Complex4

  • MT-C4D

  • Complex Iv Mitochondrial Respiratory Chain Deficiency

  • Lethal Neonatal Cardiomyopathy Hypertrophic Due To Cytochrome C Oxidase Deficiency

  • Mitochondrial Complex Iv Deficiency, Nuclear, Type 1

Familial Hypercholesterolemia
  • Hyperlipoproteinemia Type Iia

  • Familial Hyperbetalipoproteinaemia

  • Familial Hypercholesteremia

  • Fredrickson Type Iia Hyperlipoproteinemia

  • Fredrickson Type Iia Lipidaemia

  • Hyperbetalipoproteinemia

  • Type Ii Hyperlipidemia

  • Familial Hypercholesterolæmia

  • Familial Hypercholesterolaemia

  • Fh

  • Hypercholesterolemia Familial

  • Hyperlipoproteinemia Type Ii

  • Hypercholesterolemia, Familial

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus AP2B1 RGD RGD:71048
Canis familiaris AP2B1 VGNC VGNC:37960
Mus musculus AP2B1 MGD MGI:1919020
Macaca mulatta AP2B1 VGNC VGNC:69964
Felis catus AP2B1 VGNC VGNC:97352
Bos taurus AP2B1 VGNC VGNC:55033
Others AP2B1 NCBI