ARL2BP - ADP ribosylation factor like GTPase 2 binding protein Gene

Also Known as BART; RP66; BART1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23568

About ARL2BP

Cytogenetic location: 16q13 Genomic coordinates (GRCh38): 16:57,245,259-57,253,635 (from NCBI)

This gene has 4 transcripts (splice variants), 228 orthologues and is associated with 3 phenotypes. Ubiquitous expression in testis (RPKM 36.7), fat (RPKM 27.6) and 25 other tissues.

Summary

ADP-ribosylation factor (ARF)-like proteins (ARLs) comprise a functionally distinct group of the ARF family of RAS-related GTPases. The protein encoded by this gene binds to ARL2.GTP with high affinity but does not interact with ARL2.GDP, activated ARF, or RHO proteins. The lack of detectable membrane association of this protein or ARL2 upon activation of ARL2 is suggestive of actions distinct from those of the ARFs. This protein is considered to be the first ARL2-specific effector identified, due to its interaction with ARL2.GTP but lack of ARL2 GTPase-activating protein activity. [provided by RefSeq, Jul 2008]

ARL2BP Products (1)

mRNA Protein Name
NM_012106.4 NP_036238.1 ADP-ribosylation factor-like protein 2-binding protein
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
11847227 GOA
enables transcription coactivator activity IMP
IMP: Inferred from mutant phenotype
18234692 GOA
Biological Process GO Annotation Evidence References Source
involved in maintenance of protein location in nucleus IMP
IMP: Inferred from mutant phenotype
18234692 GOA
involved in positive regulation of tyrosine phosphorylation of STAT protein IMP
IMP: Inferred from mutant phenotype
18234692 GOA
Cellular Component GO Annotation Evidence References Source
located in centrosome IDA
IDA: Inferred from direct assay
16525022 GOA
located in midbody IDA
IDA: Inferred from direct assay
16525022 GOA
located in mitochondrial intermembrane space IDA
IDA: Inferred from direct assay
11809823 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

ARL2BP Protein Structure

ARL2_Bind_BART

ARL2_Bind_BART: The ARF-like 2 binding protein BART (20 - 134)

  • 0
  • 100
  • 163 a.a.
Protein Preferred Names Protein Names

ADP-ribosylation factor-like protein 2-binding protein

  • ADP-ribosylation factor like 2 binding protein

ARL2BP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ARL2BP Q9Y2Y0 CFAP20 Homo sapiens Q9Y6A4 33961781
Intra
ARL2BP Q9Y2Y0 CFAP20 Homo sapiens Q9Y6A4 32296183
Intra
ARL2BP Q9Y2Y0 BAG6 Homo sapiens P46379-2 32814053
Intra
ARL2BP Q9Y2Y0 BAG6 Homo sapiens P46379-2 32814053
Intra
ARL2BP Q9Y2Y0 BAG6 Homo sapiens P46379-2 32814053
Intra
ARL2BP Q9Y2Y0 q9y649_human Homo sapiens Q9Y649 32814053
Intra
ARL2BP Q9Y2Y0 q9y649_human Homo sapiens Q9Y649 32814053
Intra
ARL2BP Q9Y2Y0 q9y649_human Homo sapiens Q9Y649 32814053
Intra
ARL2BP Q9Y2Y0 FGFR3 Homo sapiens P22607 32814053
Intra
ARL2BP Q9Y2Y0 FGFR3 Homo sapiens P22607 32814053
Intra
ARL2BP Q9Y2Y0 FGFR3 Homo sapiens P22607 32814053
Intra
ARL2BP Q9Y2Y0 GSN Homo sapiens P06396 32814053
Intra
ARL2BP Q9Y2Y0 GSN Homo sapiens P06396 32814053
Intra
ARL2BP Q9Y2Y0 GSN Homo sapiens P06396 32814053
Intra
ARL2BP Q9Y2Y0 ARL3 Homo sapiens P36405 32296183
Intra
ARL2BP Q9Y2Y0 ARL3 Homo sapiens P36405 32296183
Intra
ARL2BP Q9Y2Y0 ARL3 Homo sapiens P36405 33961781
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 27107012
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 32296183
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 33961781
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 19368893
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 21988832
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404
GMS
19368893
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 19368893
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 25416956
Intra
ARL2BP Q9Y2Y0 ARL2 Homo sapiens P36404 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ARL2BP Proteins

Cat. No. Product Name Accession Purity
HY-P71660 ARL2BP Protein, Human (GST) Q9Y2Y0-1 (M1-H163) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P76156 ARL2BP Protein, Human (His) Q9Y2Y0-1 (M1-H163) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Retinitis Pigmentosa 82 With Or Without Situs Inversus
  • Retinitis Pigmentosa With Or Without Situs Inversus

  • RP82

  • Retinitis Pigmentosa, With/Without Situs Inversus

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Cone-Rod Dystrophy 2
  • Cone-Rod Dystrophy

  • CORD2

  • Cone-Rod Retinal Dystrophy

  • Rcrd2

  • Cone-Rod Retinal Dystrophy 2

  • Crd2

  • Cord

  • Crd

  • Retinal Cone-Rod Dystrophy

  • Cone-Rod Retinal Dystrophy-2

  • Retinal Cone-Rod Dystrophy 2

  • Tapetoretinal Degeneration

  • Cone-Rod Degeneration

  • Cone Rod Dystrophy

  • Dystrophy, Cone-Rod

  • Dystrophy, Cone-Rod, Type 2

  • Retinitis Pigmentosa

  • Retinitis Pigmentosa 2

  • Progressive Cone-Rod Dystrophy

Retinitis Pigmentosa 66
  • RP66

  • Retinitis Pigmentosa, Type 66

Ciliary Dyskinesia, Primary, 43
  • CILD43

  • Primary Ciliary Dyskinesia 43

  • Ciliary Dyskinesia, Primary, 43, With Or Without Situs Inversus

  • Primary Ciliary Dyskinesia 43 With Or Without Situs Inversus

  • Ciliary Dyskinesia, Primary, 43 With Or Without Situs Inversus

Fundus Dystrophy
  • Retinal Dystrophy

  • Retinal Dystrophies

  • Dystrophy, Retinal

Retinitis Pigmentosa 74
  • RP74

  • Retinitis Pigmentosa, Type 74

Oral Hairy Leukoplakia
  • Hairy Leukoplakia

  • Leukoplakia, Hairy

  • Hairy Leucoplakia

Situs Inversus
  • Situs Inversus Viscerum

  • Laterality Sequence

  • Complete Transposition

  • Siv

Nasopharyngeal Carcinoma
  • Malignant Neoplasm Of Nasopharynx

  • Npc

  • Nasopharyngeal Cancer

  • Nasopharyngeal Carcinoma 1

  • Nasopharynx Carcinoma

  • Nasopharyngeal Neoplasms

  • Npca

  • Carcinoma Of Nasopharynx

  • Malignant Nasopharyngeal Tumor

  • Nasopharynx Cancer

  • Squamous Cell Carcinoma Of The Nasopharynx

  • Nasopharyngeal Neoplasm

  • Cancer Of Nasopharynx

Keratinizing Squamous Cell Carcinoma
  • Squamous Cell Carcinoma, Keratinizing

  • Keratinizing Epidermoid Carcinoma

Pfeiffer Syndrome
  • Infectious Mononucleosis

  • Acs5

  • Craniofacial-Skeletal-Dermatologic Dysplasia

  • Acs V

  • Noack Syndrome

  • Gammaherpesviral Mononucleosis

  • Acrocephalosyndactyly Type 5

  • Pfeiffer Syndrome Type 3

  • Acrocephalosyndactyly, Type V

  • Glandular Fever

  • Pfeiffer Type Acrocephalosyndactyly

  • Pfeiffer Syndrome Type 2

  • Acrocephalosyndactylia Type V

  • Filatov'S Disease

  • Monocytic Angina

  • Mononucleosis

  • Pfeiffer'S Disease

  • Acsv

  • Acrocephalosyndactyly, Type 5

  • Craniofacial-Skeletal-Dermatologic Syndrome

  • Pfeiffer Syndrome Type 1

  • Classic Pfeiffer Syndrome

  • PS

  • Pfeiffer Syndrome Variant

  • Dysplasia, Craniofacial-Skeletal-Dermatologic

  • Pfeiffer

  • Kissing Disease

  • Infectious Adenitis

  • Pfeiffer Disease

Bare Lymphocyte Syndrome, Type I
  • Hla Class I Deficiency

  • Mhc Class I Deficiency

  • Bls, Type I

  • Bare Lymphocyte Syndrome Type I

  • Bare Lymphocyte Syndrome, Type I, Due To Tap2 Deficiency

  • Blsi

  • Mhc Class 1 Deficiency

  • Major Histocompatibility Complex Class 1 Deficiency

  • Bare Lymphocyte Syndrome 1

  • BLS1

  • Bls I

  • Bls Type I

  • Bl-1

  • Bare Lymphocyte Syndrome Type 1

  • Immunodeficiency By Defective Expression Of Hla - [Human Leukocyte Antigen] Class 1

  • Scid - [Severe Combined Immunodeficiency] Due To Absent Class 2 Hla Antigens

  • Bls - [Bare Lymphocyte Syndrome] Nos

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
Macaca mulatta ARL2BP VGNC VGNC:104681
Mus musculus ARL2BP MGD MGI:1349429
Bos taurus ARL2BP VGNC VGNC:26142
Rattus norvegicus ARL2BP RGD RGD:1561471
Canis familiaris ARL2BP VGNC VGNC:38110
Others ARL2BP NCBI