MBLAC2 - metallo-beta-lactamase domain containing 2 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 153364

About MBLAC2

This gene has 2 transcripts (splice variants), 199 orthologues and 4 paralogues. Ubiquitous expression in brain (RPKM 4.5), ovary (RPKM 4.5) and 25 other tissues.

Summary

Enables palmitoyl-CoA hydrolase activity. Located in endoplasmic reticulum membrane and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

MBLAC2 Products (1)

mRNA Protein Name
NM_203406.2 NP_981951.2 acyl-coenzyme A thioesterase MBLAC2
Molecular Function GO Annotation Evidence References Source
enables beta-lactamase activity IDA
IDA: Inferred from direct assay
31434986 GOA
enables long-chain fatty acyl-CoA hydrolase activity IMP
IMP: Inferred from mutant phenotype
33219126 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Cellular Component GO Annotation Evidence References Source
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
33219126 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
33219126 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

MBLAC2 Protein Structure

Lactamase_B

Lactamase_B: Metallo-beta-lactamase superfamily (30 - 218)

  • 0
  • 100
  • 200
  • 279 a.a.
Protein Preferred Names Protein Names

acyl-coenzyme A thioesterase MBLAC2

  • acyl-CoA thioesterase MBLAC2

MBLAC2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MBLAC2 Q68D91 PBX3 Homo sapiens Q96AL5 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Jalili Syndrome
  • Cone-Rod Dystrophy And Amelogenesis Imperfecta

  • Cone Rod Dystrophy-Amelogenesis Imperfecta Syndrome

  • Cone-Rod Dystrophy Amelogenesis Imperfecta

  • Cone-Rod Dystrophy With Amelogenesis Imperfecta

  • JALIS

  • Cone Rod Dystrophy Amelogenesis Imperfecta

Usher Syndrome, Type Iic
  • Usher Syndrome Type 2c

  • USH2C

  • Usher Syndrome, Type 2c

  • Usher Syndrome, Type Iic, Gpr98/Pdzd7 Digenic

  • Usher Syndrome Type Iic

  • Usher Syndrome, Type 2c, Gpr98/Pdzd7 Digenic

  • Usher Syndrome 2c

  • Usher'S Syndrome Type 2c

  • Usher Syndrome Type Iic Gpr98/Pdzd7 Digenic

Tetralogy Of Fallot
  • TOF

  • Fallot Tetralogy

  • Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

  • Tetrad Of Fallot

  • Fallot Tetrad

  • Fallot Disease

  • Fallot Complex

  • Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

  • Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

  • Interventricular Septal Defect, In Tetralogy Of Fallot

  • Ventricular Septal Defect With Obstructed Right Ventricular Outflow

  • Tof - [Tetralogy Of Fallot]

  • Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

  • Pulmonary Atresia, Ventricular Septal Defect And Mapcas

  • Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]

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 MBLAC2 VGNC VGNC:110452
Mus musculus MBLAC2 MGD MGI:1920102
Bos taurus MBLAC2 VGNC VGNC:31282
Felis catus MBLAC2 VGNC VGNC:63400
Canis familiaris MBLAC2 VGNC VGNC:43056
Rattus norvegicus MBLAC2 RGD RGD:1306703
Others MBLAC2 NCBI