WASL - WASP like actin nucleation promoting factor Gene

Also Known as NWASP; WASPB; N-WASP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8976

About WASL

Cytogenetic location: 7q31.32 Genomic coordinates (GRCh38): 7:123,681,943-123,749,003 (from NCBI)

This gene has 1 transcript (splice variant), 256 orthologues and 1 paralogue. Ubiquitous expression in colon (RPKM 25.7), thyroid (RPKM 23.4) and 25 other tissues.

Summary

This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin Cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013]

WASL Products (1)

mRNA Protein Name
NM_003941.4 NP_003932.3 actin nucleation-promoting factor WASL
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11231575 GOA
Biological Process GO Annotation Evidence References Source
involved in actin filament polymerization IDA
IDA: Inferred from direct assay
16767080 GOA
involved in negative regulation of lymphocyte migration IMP
IMP: Inferred from mutant phenotype
22585739 GOA
involved in negative regulation of membrane tubulation IDA
IDA: Inferred from direct assay
18388313 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
16767080 GOA
Cellular Component GO Annotation Evidence References Source
located in cytosol IDA
IDA: Inferred from direct assay
18388313 GOA
located in nucleus IDA
IDA: Inferred from direct assay
16767080 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

WASL Protein Structure

WH1

WH1: WH1 domain (32 - 136)

PBD

PBD: P21-Rho-binding domain (202 - 260)

WH2

WH2: WH2 motif (404 - 427)

WH2

WH2: WH2 motif (431 - 450)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
Protein Preferred Names Protein Names

actin nucleation-promoting factor WASL

  • Wiskott-Aldrich syndrome like

WASL Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
WASL O00401 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
WASL O00401 ARHGAP12 Homo sapiens Q8IWW6-4 32296183
Intra
WASL O00401 SORBS2 Homo sapiens O94875-10 32296183
Intra
WASL O00401 SORBS3 Homo sapiens O60504-2 18662323
Intra
WASL O00401 UBASH3B Homo sapiens Q8TF42 32296183
Intra
WASL O00401 PTK6 Homo sapiens Q13882 25416956
Intra
WASL O00401 PTK6 Homo sapiens Q13882 25416956
Intra
WASL O00401 NCK1 Homo sapiens P16333-1 16595635
Cross
WASL O00401 espF(U) Escherichia coli O157:H7 Q8X482 15296718
Cross
WASL O00401 espF(U) Escherichia coli O157:H7 Q8X482
IF
15296718
Intra
WASL O00401 WIPF2 Homo sapiens Q8TF74 33961781
Intra
WASL O00401 WIPF2 Homo sapiens Q8TF74 28514442
Intra
WASL O00401 WIPF2 Homo sapiens Q8TF74 32296183
Intra
WASL O00401 WIPF2 Homo sapiens Q8TF74 35271311
Intra
WASL O00401 WIPF2 Homo sapiens Q8TF74 23414517
Intra
WASL O00401 WIPF1 Homo sapiens O43516 35271311
Intra
WASL O00401 WIPF1 Homo sapiens O43516 16582881
Intra
WASL O00401 WIPF1 Homo sapiens O43516 33961781
Intra
WASL O00401 WIPF1 Homo sapiens O43516
Y2H
11331876
Intra
WASL O00401 WIPF1 Homo sapiens O43516 25416956
Intra
WASL O00401 WIPF1 Homo sapiens O43516 28514442
Intra
WASL O00401 WIPF1 Homo sapiens O43516 23414517
Intra
WASL O00401 ARPC3 Homo sapiens O15145 32296183
Intra
WASL O00401 ARPC3 Homo sapiens O15145 25416956
Intra
WASL O00401 ARPC3 Homo sapiens O15145 25416956
Intra
WASL O00401 ARPC4 Homo sapiens P59998 32296183
Intra
WASL O00401 CIB1 Homo sapiens Q99828
Y2H
16582881
Intra
WASL O00401 CIB1 Homo sapiens Q99828 16582881
Intra
WASL O00401 RNF8 Homo sapiens O76064 31515488
Intra
WASL O00401 RNF8 Homo sapiens O76064 25416956
Intra
WASL O00401 RNF8 Homo sapiens O76064 32296183
Intra
WASL O00401 RNF8 Homo sapiens O76064 25416956
Intra
WASL O00401 RNF8 Homo sapiens O76064 25416956
Intra
WASL O00401 NCK1 Homo sapiens P16333 17474147
Intra
WASL O00401 WIPF3 Homo sapiens A6NGB9 33961781
Intra
WASL O00401 WIPF3 Homo sapiens A6NGB9 28514442
Intra
WASL O00401 WIPF3 Homo sapiens A6NGB9 35271311
Intra
WASL O00401 GRB2 Homo sapiens P62993 20936779
Intra
WASL O00401 GRB2 Homo sapiens P62993 25416956
Intra
WASL O00401 RHOJ Homo sapiens Q9H4E5 32296183
Intra
WASL O00401 TRIP10 Homo sapiens Q15642-2 32296183
Intra
WASL O00401 NCK2 Homo sapiens O43639 25416956
Intra
WASL O00401 PAK4 Homo sapiens O96013 29100370
Intra
WASL O00401 SDCBP Homo sapiens O00560 25416956
Intra
WASL O00401 SDCBP Homo sapiens O00560 25416956
Intra
WASL O00401 SDCBP Homo sapiens O00560 32296183
Intra
WASL O00401 UBASH3A Homo sapiens P57075-2 32296183
Intra
WASL O00401 PACSIN2 Homo sapiens Q9UNF0 32296183
Intra
WASL O00401 PACSIN3 Homo sapiens Q9UKS6 32296183
Intra
WASL O00401 CDC42 Homo sapiens P60953 15834156
Cross
WASL O00401 Fnbp1 Rattus norvegicus Q8R511 14732713
Cross
WASL O00401 ACTR3 Bos taurus P61157 16253999
Cross
WASL O00401 ACTR3 Bos taurus P61157 11231575
Cross
WASL O00401 ACTR3 Bos taurus P61157 12732638
Cross
WASL O00401 ACTA1 Oryctolagus cuniculus P68135 11231575
Cross: Cross-species interaction Intra: Intraspecies interaction

WASL Antibodies

Cat. No. Product Name Application Reactivity
HY-P81720 N WASP Antibody (YA1465) WB, IHC-F, IHC-P, ICC/IF Human, Mouse
HY-P81720A N WASP Antibody (YA1465)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human, Mouse

Related Diseases

Diseases Alias
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

Buruli Ulcer
  • Buruli Ulcer, Susceptibility To

  • Buruli Ulcer Disease

  • Mycobacterium Ulcerans

  • Mycobacterium Ulcerans, Susceptibility To

  • Bairnsdale Ulcer

  • Daintree Ulcer

  • Mossman Ulcer

  • Searl Ulcer

  • Searle'S Ulcer

  • Bud

Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2
  • Aoa2

  • Ataxia With Oculomotor Apraxia Type 2

  • Scar1

  • SCAN2

  • Ataxia-Oculomotor Apraxia 2

  • Ataxia-Ocular Apraxia 2

  • Ataxia-Oculomotor Apraxia Type 2

  • Scan 2

  • Spinocerebellar Ataxia With Axonal Neuropathy Type 2

  • Spinocerebellar Ataxia, Autosomal Recessive 1, Formerly

  • Scar1, Formerly

  • Autosomal Recessive Spinocerebellar Ataxia-1

  • Spinocerebellar Ataxia, Autosomal Recessive, 1

  • Ataxia-Ocular Apraxia-2

  • Spinocerebellar Ataxia, Autosomal Recessive 1

Vaccinia
Myopathy, Centronuclear, 2
  • Myopathy, Centronuclear, Autosomal Recessive

  • Autosomal Recessive Centronuclear Myopathy

  • CNM2

  • Centronuclear Myopathy 2

  • Ar-Cnm

  • Myotubular Myopathy, Autosomal Recessive

  • Autosomal Recessive Myotubular Myopathy

  • Centronuclear Myopathy Autosomal Recessive

  • Myopathy, Centronuclear, Type 2

Lower Lip Cancer
Aarskog-Scott Syndrome
  • Aarskog Syndrome

  • Faciogenital Dysplasia

  • Faciodigitogenital Syndrome

  • AAS

  • Fgdy

  • X-Linked Aarskog Syndrome

  • Intellectual Developmental Disorder, X-Linked, Syndromic 16

  • Aarskog Syndrome, X-Linked

  • Intellectual Developmental Disorder, X-Linked Syndromic 16

  • Greig'S Syndrome

  • Aarskog Scott Syndrome

  • Aarskog Disease

  • Scott Aarskog Syndrome

  • Facio-Digito-Genital Dysplasia

  • Faciogenital Dysplasia With Attention Deficit-Hyperactivity Disorder

  • Aarskog-Scott Syndrome ) Syndrome

Frank-Ter Haar Syndrome
  • Ter Haar Syndrome

  • Borrone Dermatocardioskeletal Syndrome

  • FTHS

  • Autosomal Recessive Melnick-Needles Syndrome

  • Borrone Di Rocco Crovato Syndrome

  • Megalocornea, Multiple Skeletal Anomalies, And Developmental Delay

  • Melnick-Needles Syndrome, Autosomal Recessive, Formerly

  • Frank Ter Haar Syndrome

Neutropenia, Severe Congenital, X-Linked
  • X-Linked Severe Congenital Neutropenia

  • XLN

  • SCNX

  • Severe Congenital Neutropenia X-Linked

  • Neutropenia, Congenital, Severe, X-Linked

Shigellosis
  • Dysentery, Bacillary

  • Bacillary Dysentery

  • Shigella Boydii Infectious Disease

  • Shigella Flexneri Infectious Disease

  • Shigella Gastroenteritis

  • Shigella Sonnei Infectious Disease

  • Shigella Infections

Otopalatodigital Syndrome Spectrum Disorder
  • Opd Spectrum Disorder

  • Opsd

  • Fronto-Otopalatodigital Osteodysplasia

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus WASL RGD RGD:735144
Mus musculus WASL MGD MGI:1920428
Canis familiaris WASL VGNC VGNC:58887
Bos taurus WASL VGNC VGNC:56336
Macaca mulatta WASL VGNC VGNC:78783
Felis catus WASL VGNC VGNC:67007
Others WASL NCBI