1. Gene
  2. DIP2A - disco interacting protein 2 homolog A Gene

DIP2A - disco interacting protein 2 homolog A Gene

中文名称:迪斯科相互作用蛋白 2 同系物 A

种属: Homo sapiens

同用名: DIP2; C21orf106

基因 ID: 23181 | 基因类型: protein coding

关于 DIP2A

Cytogenetic location: 21q22.3 Genomic coordinates (GRCh38): 21:46,458,891-46,583,871 (from NCBI)

This gene has 13 transcripts (splice variants), 189 orthologues and 2 paralogues. Ubiquitous expression in spleen (RPKM 7.3), prostate (RPKM 6.1) and 25 other tissues.

功能概要

由该基因编码的蛋白质可能参与中枢神经系统的轴突模式化。该基因表达不高。已发现该基因编码不同亚型的几种转录变体。[RefSeq 提供,2009 年 3 月]

The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

DIP2A 基因产物(10)

mRNA Protein Name
NM_001146115.2 NP_001139587.1 disco-interacting protein 2 homolog A isoform f
NM_001146116.2 NP_001139588.1 disco-interacting protein 2 homolog A isoform g
NM_001353942.2 NP_001340871.1 disco-interacting protein 2 homolog A isoform h
NM_001353943.2 NP_001340872.1 disco-interacting protein 2 homolog A isoform a
NM_001353944.2 NP_001340873.1 disco-interacting protein 2 homolog A isoform i
NM_001410751.1 NP_001397680.1 disco-interacting protein 2 homolog A isoform j
NM_015151.4 NP_055966.2 disco-interacting protein 2 homolog A isoform a
NM_206889.3 NP_996772.1 disco-interacting protein 2 homolog A isoform b
NM_206890.3 NP_996773.1 disco-interacting protein 2 homolog A isoform c
NM_206891.3 NP_996774.1 disco-interacting protein 2 homolog A isoform d
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 protein binding IPI
IPI: 通过物理相互作用推断
20054002 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of gene expression IDA
IDA: 通过直接分析推断
20860622 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cell surface IDA
IDA: 通过直接分析推断
20054002 GOA
located in membrane IDA
IDA: 通过直接分析推断
20054002 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

DIP2A 蛋白结构

DMAP_binding

DMAP_binding: DMAP1-binding Domain (10 - 122)

AMP-binding

AMP-binding: AMP-binding enzyme (341 - 813)

AMP-binding

AMP-binding: AMP-binding enzyme (992 - 1437)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1571 a.a.
蛋白主名 其他名称

disco-interacting protein 2 homolog A

DIP2 disco-interacting protein 2 homolog A

DIP2A 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
DIP2A Q14689 FST Homo sapiens P19883
Competition Binding
20860622
种属内
DIP2A Q14689 FSTL1 Homo sapiens Q12841
Y2H
20860622
种属间
DIP2A Q14689 Fstl1 Mus musculus Q62356
Anti Tag CoIP
20054002
种属内
DIP2A Q14689 TRIP13 Homo sapiens Q15645
Validated Y2H
25416956
种属内
DIP2A Q14689 TRIP13 Homo sapiens Q15645
Y2H Array
25416956
种属内
DIP2A Q14689 TRIP13 Homo sapiens Q15645
Y2H Prey Pooling
25416956
种属内
DIP2A Q14689 GPATCH2L Homo sapiens Q9NWQ4
Y2H Prey Pooling
25416956
种属内
DIP2A Q14689 GPATCH2L Homo sapiens Q9NWQ4
Y2H Array
25416956
种属内
DIP2A Q14689 CEP44 Homo sapiens Q9C0F1
Y2H Prey Pooling
25416956
种属内
DIP2A Q14689 ATOSB Homo sapiens Q7L5A3
Y2H Prey Pooling
25416956
种属内
DIP2A Q14689 ATOSB Homo sapiens Q7L5A3
Validated Y2H
25416956
种属内
DIP2A Q14689 ATOSB Homo sapiens Q7L5A3
Y2H Array
25416956
种属内
DIP2A Q14689 TGFB1 Homo sapiens P01137
SPR
20860622
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
Malignant Histiocytic Disease

Histiocytic Disorders, Malignant

Dyslexia
Hermansky-Pudlak Syndrome 5

HPS5

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial

Delta Storage Pool Disease

Hermansky-Pudlak Syndrome, Type 5

Platelet Storage Pool Deficiency

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Reading Disorder

Specific Reading Disorder

Reading

Dyslexia

Developmental Reading Disorder

Middle Cerebral Artery Infarction

Infarction, Middle Cerebral Artery

Infarction Middle Cerebral Artery

Learning Disability

Learning Disabilities

Learning Disorders

Academic Skill Disorder

Learning Disorder

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Chromosome 22q11.2 Deletion Syndrome, Distal

22q11.2 Deletion Syndrome

Autosomal Dominant Opitz G/Bbb Syndrome

Catch22

Cayler Cardiofacial Syndrome

Conotruncal Anomaly Face Syndrome

Digeorge Syndrome

Sedlackova Syndrome

Shprintzen Syndrome

Velocardiofacial Syndrome

22q11.2 Distal Deletion Syndrome

Distal 22q11.2 Microdeletion Syndrome

22q11.2ds

Vcfs

Velo-Cardio-Facial Syndrome

Distal Chromosome 22q11.2 Deletion Syndrome

Chromosome 22q11.2 Deletion Syndrome Distal

Chromosome 22q11.2 Deletion Syndrome

Deletion 22q11.2 Syndrome

22q11ds

Catch 22

Digeorge Sequence

Microdeletion 22q11.2

Monosomy 22q11

Takao Syndrome

Distal Del(22)(Q11.2)

Distal Monosomy 22q11.2

Catch 22 Syndrome

Chromosome Deletion Syndrome 22q11.2, Distal

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 DIP2A VGNC VGNC:28066
Macaca mulatta DIP2A VGNC VGNC:71641
Felis catus DIP2A VGNC VGNC:61492
Rattus norvegicus DIP2A RGD RGD:1582897
Mus musculus DIP2A MGD MGI:2385920