1. Gene
  2. PACSIN2 - protein kinase C and casein kinase substrate in neurons 2 Gene

PACSIN2 - protein kinase C and casein kinase substrate in neurons 2 Gene

中文名称:神经元中的蛋白激酶 C 和酪蛋白激酶底物 2

种属: Homo sapiens

同用名: SDPII

基因 ID: 11252 | 基因类型: protein coding

关于 PACSIN2

Cytogenetic location: 22q13.2 Genomic coordinates (GRCh38): 22:42,869,766-43,015,149 (from NCBI)

This gene has 12 transcripts (splice variants), 209 orthologues and 2 paralogues. Ubiquitous expression in adrenal (RPKM 24.2), colon (RPKM 24.1) and 25 other tissues.

功能概要

该基因是神经元家族中蛋白激酶 C 和酪蛋白激酶底物的成员。编码的蛋白质通过调节微管蛋白聚合参与连接肌动蛋白细胞骨架和囊泡形成。可变剪接导致多个转录本变体。[RefSeq 提供,2010 年 5 月]

This gene is a member of the protein kinase C and Casein Kinase substrate in neurons family. The encoded protein is involved in linking the actin Cytoskeleton with vesicle formation by regulating tubulin polymerization. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

PACSIN2 基因产物(10)

mRNA Protein Name
NM_001184970.3 NP_001171899.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform A
NM_001184971.1 NP_001171900.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform B
NM_001349968.1 NP_001336897.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform C
NM_001349969.2 NP_001336898.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform D
NM_001349970.2 NP_001336899.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform D
NM_001349971.2 NP_001336900.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform C
NM_001349972.1 NP_001336901.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform C
NM_001349973.1 NP_001336902.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform C
NM_001349974.2 NP_001336903.1 protein kinase C and casein kinase substrate in neurons protein 2 isoform E
NM_007229.3 NP_009160.2 protein kinase C and casein kinase substrate in neurons protein 2 isoform A
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables identical protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
enables phosphatidic acid binding IDA
IDA: 通过直接分析推断
23596323 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in caveola assembly IMP
IMP: 通过突变表型推断
21610094 GOA
involved in caveolin-mediated endocytosis IMP
IMP: 通过突变表型推断
21610094 GOA
involved in plasma membrane tubulation IDA
IDA: 通过直接分析推断
23596323 GOA
involved in protein localization to endosome IMP
IMP: 通过突变表型推断
23596323 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in caveola IDA
IDA: 通过直接分析推断
21610094 GOA
located in recycling endosome membrane IDA
IDA: 通过直接分析推断
23596323 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PACSIN2 蛋白结构

FCH

FCH: Fes/CIP4, and EFC/F-BAR homology domain (16 - 103)

SH3_9

SH3_9: Variant SH3 domain (433 - 483)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 486 a.a.
蛋白主名 其他名称

protein kinase C and casein kinase substrate in neurons protein 2

cytoplasmic phosphoprotein PACSIN2

PACSIN2 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
PACSIN2 Q9UNF0 PBX4 Homo sapiens Q9BYU1 32296183
种属内
PACSIN2 Q9UNF0 PBX4 Homo sapiens Q9BYU1 32296183
种属内
PACSIN2 Q9UNF0 MEOX2 Homo sapiens Q6FHY5 32296183
种属内
PACSIN2 Q9UNF0 MEOX2 Homo sapiens Q6FHY5 32296183
种属内
PACSIN2 Q9UNF0 GSC2 Homo sapiens O15499 32296183
种属内
PACSIN2 Q9UNF0 GSC2 Homo sapiens O15499 32296183
种属内
PACSIN2 Q9UNF0 COBL Homo sapiens O75128 35271311
种属内
PACSIN2 Q9UNF0 COBL Homo sapiens O75128 33961781
种属内
PACSIN2 Q9UNF0 DNM2 Homo sapiens P50570 16551695
种属内
PACSIN2 Q9UNF0 FASLG Homo sapiens P48023 16318909
种属内
PACSIN2 Q9UNF0 FASLG Homo sapiens P48023 16318909
种属内
PACSIN2 Q9UNF0 FASLG Homo sapiens P48023 16318909
种属内
PACSIN2 Q9UNF0 TERF1 Homo sapiens P54274 21044950
种属内
PACSIN2 Q9UNF0 PACSIN1 Homo sapiens Q9BY11 32296183
种属内
PACSIN2 Q9UNF0 PACSIN1 Homo sapiens Q9BY11 16189514
种属内
PACSIN2 Q9UNF0 PACSIN1 Homo sapiens Q9BY11 32296183
种属内
PACSIN2 Q9UNF0 PACSIN1 Homo sapiens Q9BY11 33961781
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 32296183
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 25416956
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 32296183
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 16189514
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 20188097
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 31515488
种属内
PACSIN2 Q9UNF0 PACSIN2 Homo sapiens Q9UNF0 32296183
种属内
PACSIN2 Q9UNF0 MEOX2 Homo sapiens P50222 25416956
种属内
PACSIN2 Q9UNF0 MEOX2 Homo sapiens P50222 25416956
种属内
PACSIN2 Q9UNF0 PACSIN3 Homo sapiens Q9UKS6 32296183
种属内
PACSIN2 Q9UNF0 PACSIN3 Homo sapiens Q9UKS6 33961781
种属内
PACSIN2 Q9UNF0 PACSIN3 Homo sapiens Q9UKS6 32296183
种属内
PACSIN2 Q9UNF0 PACSIN3 Homo sapiens Q9UKS6 35271311
种属内
PACSIN2 Q9UNF0 RIC8A Homo sapiens Q9NPQ8-4 32296183
种属内
PACSIN2 Q9UNF0 RIC8A Homo sapiens Q9NPQ8-4 32296183
种属内
PACSIN2 Q9UNF0 WASL Homo sapiens O00401 32296183
种属内
PACSIN2 Q9UNF0 WASL Homo sapiens O00401 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 PACSIN2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71184 PACSIN2 Protein, Human (HEK293, His) Q9UNF0-1 (M1-Q486) ≥95%

关联疾病

疾病名称 别名
Thiopurines, Poor Metabolism Of, 1

Thiopurine S-Methyltransferase Deficiency

Tpmt Deficiency

Thiopurine Methyltransferase Deficiency

Thiopurine S Methyltranferase Deficiency

THPM1

Tpmtd

Poor Metabolism Of Thiopurines-1

6-Mercaptopurine Sensitivity

Thiopurines, Poor Metabolism Of

Poor Metabolism Of Thiopurines

Microvillus Inclusion Disease

Congenital Microvillous Atrophy

Intractable Diarrhea Of Infancy

Congenital Familial Protracted Diarrhea With Enterocyte Brush-Border Abnormalities

Davidson Disease

Microvillous Inclusion Disease

Congenital Microvillus Atrophy

Mvid

Diarrhea 2 With Microvillus Atrophy

Mvd

Congenital Familial Protracted Diarrhea

Davidson'S Disease

Familial Enteropathy, Microvillus

Microvillus Atrophy, Congenital

Congenital Enteropathy

Familial Protracted Enteropathy

Microvillous Atrophy

Microvillus Atrophy With Diarrhea 2

Idi

Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive

Charcot-Marie-Tooth Disease Type 4

Charcot-Marie-Tooth Disease Type 4e

Hereditary Motor And Sensory Neuropathy

Cmt4e

CHN1

Hypomyelinating Neuropathy, Congenital, 1

Charcot-Marie-Tooth Neuropathy Type 4e

Neuropathy, Congenital Hypomyelinating, 1

Ar-Cmt1

Autosomal Recessive Demyelinating Charcot-Marie-Tooth

Cmt4

Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive

Hypomyelination, Severe Congenital

Charcot-Marie-Tooth Disease, Type 4e

Charcot-Marie-Tooth Neuropathy, Type 4e

Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy

Autosomal Recessive Congenital Hypomyelinating Neuropathy

Congenital Amyelinating Neuropathy

Congenital Hypomyelinating Neuropathy Autosomal Recessive

Neuropathy, Congenital Hypomyelinating Or Amyelinating

Severe Congenital Hypomyelination

Hereditary Sensory Motor Neuropathy

Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive

Neuropathy, Hypomyelinating, Congenital, Type 1

Neuropathy, Motor And Sensory, Hereditary

Congenital Hypomyelinating Neuropathy

Hereditary Motor And Sensory Neuropathies

Hereditary Sensorimotor Neuropathy

Hmsn - [Hereditary Motor And Sensory Neuropathy]

Hsmn - [Hereditary Sensory And Motor Neuropathy]

Hereditary Motor And Sensory Neuropathy, Types I-Iv

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 PACSIN2 RGD RGD:69411
Mus musculus PACSIN2 MGD MGI:1345153
Canis familiaris PACSIN2 VGNC VGNC:44232
Bos taurus PACSIN2 VGNC VGNC:32543
Felis catus PACSIN2 VGNC VGNC:68682
Macaca mulatta PACSIN2 VGNC VGNC:75745
Others PACSIN2 NCBI