1. Gene
  2. NECAP2 - NECAP endocytosis associated 2 Gene

NECAP2 - NECAP endocytosis associated 2 Gene

中文名称:NECAP 内吞作用相关 2

种属: Homo sapiens

基因 ID: 55707 | 基因类型: protein coding

关于 NECAP2

Cytogenetic location: 1p36.13 Genomic coordinates (GRCh38): 1:16,440,724-16,460,078 (from NCBI)

This gene has 12 transcripts (splice variants), 208 orthologues and 1 paralogue. Ubiquitous expression in lymph node (RPKM 34.8), spleen (RPKM 33.6) and 25 other tissues.

功能概要

该基因可能编码适应蛋白耳结合外壳相关蛋白家族的成员。对大鼠中类似蛋白质的研究表明其在网格蛋白介导的内吞作用中起作用。已经描述了选择性剪接的转录物变体。[RefSeq 提供,2009 年 2 月]

This gene likely encodes a member of the adaptin-ear-binding coat-associated protein family. Studies of a similar protein in rat suggest a role in clathrin-mediated endocytosis. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]

NECAP2 基因产物(3)

mRNA Protein Name
NM_001145277.2 NP_001138749.1 adaptin ear-binding coat-associated protein 2 isoform 2
NM_001145278.2 NP_001138750.1 adaptin ear-binding coat-associated protein 2 isoform 3
NM_018090.5 NP_060560.1 adaptin ear-binding coat-associated protein 2 isoform 1
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
16189514 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

NECAP2 蛋白结构

DUF1681

DUF1681: Protein of unknown function (DUF1681) (6 - 163)

  • 0
  • 100
  • 200
  • 263 a.a.
蛋白主名 其他名称

adaptin ear-binding coat-associated protein 2

adaptin-ear-binding coat-associated protein 2

NECAP2 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
NECAP2 Q9NVZ3 AP2B1 Homo sapiens P63010 33961781
种属内
NECAP2 Q9NVZ3 AP2B1 Homo sapiens P63010 35271311
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 NECAP2 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70922 NECAP2 Protein, Human (His) Q9NVZ3 (M1-F263) ≥ 95%, as determined by reducing SDS-PAGE.

关联疾病

疾病名称 别名
Lissencephaly 8

LIS8

Congenital Anomalies Of Kidney And Urinary Tract 1

CAKUT1

Renal Hypodysplasia, Nonsyndromic, 1

Rhdns1

Congenital Anomalies Of The Kidney And Urinary Tract 1

Non-Syndromic Renal Hypodysplasia 1

Kidney And Urinary Tract, Anomalies, Congenital, Susceptibility To, Type 1

Spinocerebellar Ataxia, Autosomal Recessive 24

SCAR24

Autosomal Recessive Spinocerebellar Ataxia 24

Spinocerebellar Ataxia, Autosomal Recessive, 24

Ataxia, Spinocerebellar, Autosomal Recessive, Type 24

Schuurs-Hoeijmakers Syndrome

SHMS

Pacs1-Related Syndrome

Mrd17

Intellectual Disability-Craniofacial Dysmorphism-Cryptorchidism Syndrome

Intellectual Developmental Disorder, Autosomal Dominant 17

Autosomal Dominant Intellectual Disability-17

Autosomal Dominant Mental Retardation 17

Pacs1 Syndrome

Mental Retardation, Autosomal Dominant 17

Early Infantile Epileptic Encephalopathy

Early Infantile Epileptic Encephalopathy With Burst-Suppression

Early Infantile Epileptic Encephalopathy With Suppression Bursts

Eiee

Early Infantile Epileptic Encephalopathy With Suppression-Bursts

Ohtahara Syndrome

Encephalopathy, Epileptic, Early Infantile

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
Bos taurus NECAP2 VGNC VGNC:31981
Rattus norvegicus NECAP2 RGD RGD:735063
Canis familiaris NECAP2 VGNC VGNC:43717
Macaca mulatta NECAP2 VGNC VGNC:75255
Mus musculus NECAP2 MGD MGI:1913397
Others NECAP2 NCBI