AIMP2 - aminoacyl tRNA synthetase complex interacting multifunctional protein 2 Gene

Also Known as P38; JTV1; HLD17; JTV-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7965

About AIMP2

Cytogenetic location: 7p22.1 Genomic coordinates (GRCh38): 7:6,009,272-6,023,834 (from NCBI)

This gene has 4 transcripts (splice variants), 219 orthologues and is associated with 1 phenotype. Ubiquitous expression in testis (RPKM 18.6), duodenum (RPKM 17.0) and 25 other tissues.

Summary

The protein encoded by this gene is part of the Aminoacyl-tRNA Synthetase complex, which contains nine different aminoacyl-tRNA synthetases and three non-enzymatic factors. The encoded protein is one of the non-enzymatic factors and is required for assembly and stability of the complex. [provided by RefSeq, May 2016]

AIMP2 Products (8)

mRNA Protein Name
NM_001326606.2 NP_001313535.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform b
NM_001326607.2 NP_001313536.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform c
NM_001326609.2 NP_001313538.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform d
NM_001326610.2 NP_001313539.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform d
NM_001326611.3 NP_001313540.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform d
NM_001362785.2 NP_001349714.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform e
NM_001362787.2 NP_001349716.1 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform f
NM_006303.4 NP_006294.2 aminoacyl tRNA synthase complex-interacting multifunctional protein 2 isoform a

AIMP2 Protein Structure

GST_C_3

GST_C_3: Glutathione S-transferase, C-terminal domain (227 - 307)

  • 0
  • 100
  • 200
  • 300
  • 320 a.a.
Protein Preferred Names Protein Names

aminoacyl tRNA synthase complex-interacting multifunctional protein 2

  • ARS-interacting multi-functional protein 2

AIMP2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
AIMP2 Q13155 NECAB2 Homo sapiens Q7Z6G3-2 25416956
Intra
AIMP2 Q13155 NECAB2 Homo sapiens Q7Z6G3-2 25416956
Intra
AIMP2 Q13155 ZGPAT Homo sapiens Q8N5A5-2 32296183
Intra
AIMP2 Q13155 ZGPAT Homo sapiens Q8N5A5-2 32296183
Intra
AIMP2 Q13155 ZGPAT Homo sapiens Q8N5A5-2 25416956
Intra
AIMP2 Q13155 ZGPAT Homo sapiens Q8N5A5-2 32296183
Intra
AIMP2 Q13155 AIMP1 Homo sapiens Q12904 25416956
Intra
AIMP2 Q13155 AIMP1 Homo sapiens Q12904 25416956
Intra
AIMP2 Q13155 KRT34 Homo sapiens O76011 32296183
Intra
AIMP2 Q13155 KRT34 Homo sapiens O76011 32296183
Intra
AIMP2 Q13155 KRT33B Homo sapiens Q14525 32296183
Intra
AIMP2 Q13155 KRT33B Homo sapiens Q14525 32296183
Intra
AIMP2 Q13155 KRT33B Homo sapiens Q14525 32296183
Intra
AIMP2 Q13155 BCAS2 Homo sapiens O75934 31515488
Intra
AIMP2 Q13155 BCAS2 Homo sapiens O75934 32296183
Intra
AIMP2 Q13155 BCAS2 Homo sapiens O75934 25416956
Intra
AIMP2 Q13155 BCAS2 Homo sapiens O75934 32296183
Intra
AIMP2 Q13155 MIS18A Homo sapiens Q9NYP9 25416956
Intra
AIMP2 Q13155 MIS18A Homo sapiens Q9NYP9 32296183
Intra
AIMP2 Q13155 MIS18A Homo sapiens Q9NYP9 25416956
Intra
AIMP2 Q13155 TFIP11 Homo sapiens Q9UBB9 25416956
Intra
AIMP2 Q13155 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
AIMP2 Q13155 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
AIMP2 Q13155 TFIP11 Homo sapiens Q9UBB9 25416956
Intra
AIMP2 Q13155 TFIP11 Homo sapiens Q9UBB9 32296183
Intra
AIMP2 Q13155 SPATA18 Homo sapiens Q8TC71 32296183
Intra
AIMP2 Q13155 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
AIMP2 Q13155 KRT36 Homo sapiens O76013-2 32296183
Intra
AIMP2 Q13155 KRT36 Homo sapiens O76013-2 32296183
Intra
AIMP2 Q13155 LMO2 Homo sapiens P25791-3 32296183
Intra
AIMP2 Q13155 LMO2 Homo sapiens P25791-3 32296183
Intra
AIMP2 Q13155 DRC12 Homo sapiens Q494R4-2 32296183
Intra
AIMP2 Q13155 DRC12 Homo sapiens Q494R4-2 32296183
Intra
AIMP2 Q13155 DRC12 Homo sapiens Q494R4-2 32296183
Intra
AIMP2 Q13155 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
AIMP2 Q13155 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
AIMP2 Q13155 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
AIMP2 Q13155 TEX12 Homo sapiens Q9BXU0 32296183
Intra
AIMP2 Q13155 AIMP1 Homo sapiens Q12904-2 32296183
Intra
AIMP2 Q13155 AIMP1 Homo sapiens Q12904-2 32296183
Intra
AIMP2 Q13155 PRKAA2 Homo sapiens P54646 25416956
Intra
AIMP2 Q13155 PRKAA2 Homo sapiens P54646 25416956
Intra
AIMP2 Q13155 PRKAA2 Homo sapiens P54646 25416956
Intra
AIMP2 Q13155 SBK3 Homo sapiens P0C264 32296183
Intra
AIMP2 Q13155 SBK3 Homo sapiens P0C264 32296183
Intra
AIMP2 Q13155 TCP11 Homo sapiens Q8WWU5-7 32296183
Intra
AIMP2 Q13155 TCP11 Homo sapiens Q8WWU5-7 32296183
Intra
AIMP2 Q13155 TCP11 Homo sapiens Q8WWU5-7 32296183
Intra
AIMP2 Q13155 PCMT1 Homo sapiens P22061 25416956
Intra
AIMP2 Q13155 PCMT1 Homo sapiens P22061 25416956
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 25416956
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 32296183
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 29997244
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 32814053
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 32296183
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 32296183
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046 29997244
Intra
AIMP2 Q13155 KARS1 Homo sapiens Q15046
Y2H
21900206
Intra
AIMP2 Q13155 PFDN6 Homo sapiens O15212 32296183
Intra
AIMP2 Q13155 PFDN6 Homo sapiens O15212 32296183
Intra
AIMP2 Q13155 DARS1 Homo sapiens P14868 25416956
Intra
AIMP2 Q13155 DARS1 Homo sapiens P14868 25416956
Intra
AIMP2 Q13155 DARS1 Homo sapiens P14868 32296183
Intra
AIMP2 Q13155 DARS1 Homo sapiens P14868
Y2H
21900206
Intra
AIMP2 Q13155 DARS1 Homo sapiens P14868 32296183
Intra
AIMP2 Q13155 TP53 Homo sapiens P04637 18695251
Intra
AIMP2 Q13155 RABEP1 Homo sapiens Q15276 32296183
Intra
AIMP2 Q13155 RABEP1 Homo sapiens Q15276 32296183
Intra
AIMP2 Q13155 RABEP1 Homo sapiens Q15276 32296183
Intra
AIMP2 Q13155 FUBP1 Homo sapiens Q96AE4
Y2H
21988832
Intra
AIMP2 Q13155 FUBP1 Homo sapiens Q96AE4
IF
21285945
Intra
AIMP2 Q13155 LNX1 Homo sapiens Q8TBB1 25416956
Intra
AIMP2 Q13155 LNX1 Homo sapiens Q8TBB1 16189514
Intra
AIMP2 Q13155 LNX1 Homo sapiens Q8TBB1 32296183
Intra
AIMP2 Q13155 LNX1 Homo sapiens Q8TBB1 25416956
Intra
AIMP2 Q13155 LNX1 Homo sapiens Q8TBB1 29892012
Intra
AIMP2 Q13155 GYS1 Homo sapiens P13807 25416956
Intra
AIMP2 Q13155 GYS1 Homo sapiens P13807 25416956
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 25416956
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 32814053
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 25416956
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 32296183
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 32296183
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 25416956
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643 32296183
Intra
AIMP2 Q13155 FHL3 Homo sapiens Q13643
Y2H
21516116
Intra
AIMP2 Q13155 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
AIMP2 Q13155 BRME1 Homo sapiens Q0VDD7 25416956
Intra
AIMP2 Q13155 BRME1 Homo sapiens Q0VDD7 16189514
Intra
AIMP2 Q13155 BRME1 Homo sapiens Q0VDD7 19060904
Intra
AIMP2 Q13155 BRME1 Homo sapiens Q0VDD7 19060904
Intra
AIMP2 Q13155 BRME1 Homo sapiens Q0VDD7 16189514
Intra
AIMP2 Q13155 EXOC8 Homo sapiens Q8IYI6 32296183
Intra
AIMP2 Q13155 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
AIMP2 Q13155 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
AIMP2 Q13155 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
AIMP2 Q13155 CEP170P1 Homo sapiens Q96L14 25416956
Intra
AIMP2 Q13155 CEP170P1 Homo sapiens Q96L14 16189514
Intra
AIMP2 Q13155 CEP170P1 Homo sapiens Q96L14 25416956
Intra
AIMP2 Q13155 C1orf216 Homo sapiens Q8TAB5 32296183
Intra
AIMP2 Q13155 TERF2IP Homo sapiens Q9NYB0 21044950
Intra
AIMP2 Q13155 NDEL1 Homo sapiens Q9GZM8 25416956
Intra
AIMP2 Q13155 KRT31 Homo sapiens Q15323 32296183
Intra
AIMP2 Q13155 KRT31 Homo sapiens Q15323 32296183
Intra
AIMP2 Q13155 KRT31 Homo sapiens Q15323 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant AIMP2 Proteins

Cat. No. Product Name Accession Purity
HY-P71538 AIMP2 Protein, Human (His) Q13155 (M1-K320) ≥ 90%, as determined by reducing SDS-PAGE.

AIMP2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P86767 AIMP2 Antibody (YA6460) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Leukodystrophy, Hypomyelinating, 17
  • HLD17

Leukodystrophy, Hypomyelinating, 3
  • Hypomyelinating Leukodystrophy 3

  • HLD3

  • Pelizaeus-Merzbacher-Like Disease Due To Aimp1 Mutation

  • Leukodystrophy, Hypomyelinating 3

  • Perinatal Sudanophilic Leukodystrophy

  • Leukodystrophy, Hypomyelinating, Type 3

  • Pelizaeus-Merzbacher-Like Disease, Autosomal Recessive, 2

Leukodystrophy, Hypomyelinating, 7, With Or Without Oligodontia And/Or Hypogonadotropic Hypogonadism
  • HLD7

  • Leukoencephalopathy-Ataxia-Hypodontia-Hypomyelination Syndrome

  • Addh

  • Leukodystrophy, Hypomyelinating, With Hypodontia And Hypogonadotropic Hypogonadism

  • 4h Syndrome

  • 4h Leukodystrophy 1

  • Hypomyelinating Leukodystrophy 7 With Or Without Oligodontia And-Or Hypogonadotropic Hypogonadism

  • Hypomyelination-Cerebellar Atrophy-Hypoplasia Of The Corpus Callosum Syndrome

  • Leukodystrophy With Oligodontia

  • Tach Syndrome

  • Tremor-Ataxia-Central Hypomyelination Syndrome

  • Leukoencephalopathy, Hypomyelinating, With Ataxia And Delayed Dentition

  • Ataxia, Delayed Dentition, And Hypomyelination

  • Ataxia-Delayed Dentition-Hypomyelination Syndrome

  • Odontoleukodystrophy

  • Dentoleukoencephalopathy

  • Hypomyelinating Leukodystrophy-Ataxia-Hypodontia-Hypomyelination Syndrome

  • Ataxia-Delayed Dentition-Hypomyelination Syndrome

  • Ataxia Delayed Dentition And Hypomyelination

  • Leukodystrophy Hypomyelinating With Hypodontia And Hypogonadotropic Hypogonadism 4h Syndrome

  • Leukoencephalopathy Hypomyelinating With Ataxia And Delayed Dentition

  • Tach

  • Tremor-Ataxia With Central Hypomyelination

  • Attention Deficit Hyperactivity Disorder

  • Leukodystrophy, Dysmyelinating, With Oligodontia

Leukodystrophy
  • Leukodystrophies

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Hypomyelinating Leukodystrophy
  • Hld

  • Leukodystrophy, Hypomyelinating

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

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 AIMP2 VGNC VGNC:69650
Bos taurus AIMP2 VGNC VGNC:25766
Mus musculus AIMP2 MGD MGI:2385237
Rattus norvegicus AIMP2 RGD RGD:1560787
Felis catus AIMP2 VGNC VGNC:80550
Others AIMP2 NCBI