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  2. AP2B1 - adaptor related protein complex 2 subunit beta 1 Gene

AP2B1 - adaptor related protein complex 2 subunit beta 1 Gene

中文名称:适配器相关蛋白复合物 2 亚基 beta 1

种属: Homo sapiens

同用名: ADTB2; AP105B; CLAPB1; AP2-BETA

基因 ID: 163 | 基因类型: protein coding

关于 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.

功能概要

由该基因编码的蛋白质是组装蛋白复合物 2 的两个大链成分之一,它用于将网格蛋白连接到包被囊泡中的受体。编码的蛋白质存在于质膜中包被囊泡的细胞质面上。已发现该基因的两个转录本变体编码不同的亚型。[RefSeq 提供,2008 年 7 月]

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 基因产物(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 蛋白结构

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)

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  • 951 a.a.
蛋白主名 其他名称

AP-2 complex subunit beta

adapter-related protein complex 2 beta subunit

AP2B1 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7-2 25416956
种属内
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7-2 25416956
种属内
AP2B1 P63010 XRCC6BP1 Homo sapiens Q8N4L5 25416956
种属内
AP2B1 P63010 TXN2 Homo sapiens Q99757 25416956
种属内
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 16189514
种属内
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 35271311
种属内
AP2B1 P63010 AP2M1 Homo sapiens Q96CW1 33961781
种属内
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
种属内
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
种属内
AP2B1 P63010 KPNA2 Homo sapiens P52292 25416956
种属内
AP2B1 P63010 SLC25A6 Homo sapiens P12236 29892012
种属内
AP2B1 P63010 SLC25A6 Homo sapiens P12236 25416956
种属内
AP2B1 P63010 SLC25A6 Homo sapiens P12236 25416956
种属内
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7 25416956
种属内
AP2B1 P63010 AFF4 Homo sapiens Q9UHB7 25416956
种属内
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5
Y2H
9341158
种属内
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5 16189514
种属内
AP2B1 P63010 AP1M1 Homo sapiens Q9BXS5 33961781
种属内
AP2B1 P63010 ITSN1 Homo sapiens Q15811 33961781
种属内
AP2B1 P63010 ITSN1 Homo sapiens Q15811 35044719
种属内
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
种属内
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
种属内
AP2B1 P63010 U2AF1 Homo sapiens Q01081 25416956
种属内
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 16189514
种属内
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 25416956
种属内
AP2B1 P63010 THAP1 Homo sapiens Q9NVV9 25416956
种属内
AP2B1 P63010 NECAP2 Homo sapiens Q9NVZ3 16189514
种属内
AP2B1 P63010 NECAP2 Homo sapiens Q9NVZ3 33961781
种属内
AP2B1 P63010 MEA1 Homo sapiens Q16626 33961781
种属内
AP2B1 P63010 MEA1 Homo sapiens Q16626 16189514
种属内
AP2B1 P63010 MEA1 Homo sapiens Q16626 16189514
种属内
AP2B1 P63010 LDLRAP1 Homo sapiens Q5SW96 16189514
种属内
AP2B1 P63010 LDLRAP1 Homo sapiens Q5SW96 25416956
种属内
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 25416956
种属内
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 25416956
种属内
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 33961781
种属内
AP2B1 P63010 AP1M2 Homo sapiens Q9Y6Q5 16189514
种属间
AP2B1 P63010 Necap1 Mus musculus Q9CR95
NMR
24130457
种属间
AP2B1 P63010 Necap1 Mus musculus Q9CR95 24130457
种属间
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092 20603002
种属间
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092
Y2H
9341158
种属间
AP2B1 P63010 Ap2m1 Rattus norvegicus P84092 25061211
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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