1. Gene
  2. WASF2 - WASP family member 2 Gene

WASF2 - WASP family member 2 Gene

中文名称:黄蜂家族成员 2

种属: Homo sapiens

同用名: IMD2; SCAR2; WASF4; WAVE2; dJ393P12.2

基因 ID: 10163 | 基因类型: protein coding

关于 WASF2

Cytogenetic location: 1p36.11 Genomic coordinates (GRCh38): 1:27,404,230-27,490,167 (from NCBI)

This gene has 2 transcripts (splice variants), 201 orthologues and 2 paralogues. Ubiquitous expression in esophagus (RPKM 43.4), ovary (RPKM 33.8) and 25 other tissues.

功能概要

该基因编码 Wiskott-Aldrich 综合征蛋白家族的成员。该基因产物是一种蛋白质,可形成连接受体激酶和肌动蛋白的多蛋白复合物。与肌动蛋白的结合通过所有家族成员的 C 端 verprolin 同源域发生。多蛋白复合物用于传递涉及细胞形状、运动或功能变化的信号。根据最近的基因组序列比较,已更改已发布的地图位置 (PMID:10381382) ,这表明表达的基因位于染色体 1,而假基因可能位于染色体 X。已发现两个编码不同亚型的转录变体对于这个基因。[RefSeq 提供,2011 年 1 月]

This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location (PMID:10381382) has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]

WASF2 基因产物(2)

mRNA Protein Name
NM_001201404.3 NP_001188333.1 actin-binding protein WASF2 isoform 2
NM_006990.5 NP_008921.1 actin-binding protein WASF2 isoform 1

WASF2 蛋白结构

WH2

WH2: WH2 motif (434 - 459)

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

actin-binding protein WASF2

WAS protein family member 2

WASF2 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
WASF2 Q9Y6W5 ABL1 Homo sapiens P00519
Anti Tag CoIP
35271311
种属内
WASF2 Q9Y6W5 SPRED1 Homo sapiens Q7Z699
Validated Y2H
32814053
种属内
WASF2 Q9Y6W5 SPRED1 Homo sapiens Q7Z699
Y2H Array
32814053
种属内
WASF2 Q9Y6W5 SPRED1 Homo sapiens Q7Z699
Y2H Pooling
32814053
种属内
WASF2 Q9Y6W5 ZDHHC17 Homo sapiens Q8IUH5
Y2H Array
24705354
种属内
WASF2 Q9Y6W5 ZDHHC17 Homo sapiens Q8IUH5
Lumier
24705354
种属内
WASF2 Q9Y6W5 BAIAP2 Homo sapiens Q9UQB8-4
Far-WB
11130076
种属内
WASF2 Q9Y6W5 BAIAP2 Homo sapiens Q9UQB8-4
Anti Tag CoIP
11130076
种属内
WASF2 Q9Y6W5 BAIAP2 Homo sapiens Q9UQB8-4
Pull Down
11130076
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
Wiskott-Aldrich Syndrome

WAS

Eczema-Thrombocytopenia-Immunodeficiency Syndrome

Immunodeficiency 2

Aldrich Syndrome

Imd2

Wiskott-Aldrich Syndrome 1

Was1

Wiskott Syndrome

Wiskott Aldrich Syndrome

Eczema Thrombocytopenia Immunodeficiency Syndrome

Imd 2

Coronin-1a Deficiency
Lymphogranuloma Venereum

Climatic Or Tropical Bubo

Durand-Nicolas-Favre Disease

Lymphogranuloma Inguinale

Poradenitis Inguinale

Strumous Bubo

Lgv

Granuloma Inguinale

Donovanosis

Pudendal Ulcer

Granuloma Inguinale Tropicum

Granuloma Pudendi Tropicum

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
Canis familiaris WASF2 VGNC VGNC:48334
Felis catus WASF2 VGNC VGNC:67003
Rattus norvegicus WASF2 RGD RGD:1307299
Mus musculus WASF2 MGD MGI:1098641
Bos taurus WASF2 VGNC VGNC:36866
Macaca mulatta WASF2 VGNC VGNC:78781