2. Gene
  3. OMA1 - OMA1 zinc metallopeptidase Gene

OMA1 - OMA1 zinc metallopeptidase Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as DAB1; MPRP1; MPRP-1; YKR087C; ZMPOMA1; peptidase; 2010001O09Rik

Gene ID: 115209 | Gene type: protein coding

About OMA1

Cytogenetic location: 1p32.2-p32.1 Genomic coordinates (GRCh38): 1:58,480,719-58,546,726 (from NCBI)

This gene has 11 transcripts (splice variants) and 198 orthologues. Ubiquitous expression in kidney (RPKM 9.7), prostate (RPKM 9.5) and 25 other tissues.

Summary

Enables metalloendopeptidase activity. Involved in several processes, including HRI-mediated signaling; proteolysis; and regulation of mitochondrion organization. Located in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Apr 2022]

OMA1 Products(1)

mRNA Protein Name
NM_145243.5 NP_660286.1 metalloendopeptidase OMA1, mitochondrial precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables metalloendopeptidase activity IDA
IDA: Inferred from direct assay
25275009 GOA
enables metalloendopeptidase activity IMP
IMP: Inferred from mutant phenotype
20038677 GOA
Biological Process GO Annotation Evidence Reference Source
involved in HRI-mediated signaling IDA
IDA: Inferred from direct assay
32132706 GOA
involved in cellular response to stress IDA
IDA: Inferred from direct assay
32132706 GOA
involved in integrated stress response signaling IDA
IDA: Inferred from direct assay
32132706 GOA
involved in mitochondrial protein processing IDA
IDA: Inferred from direct assay
25275009 GOA
involved in mitochondrial protein processing IMP
IMP: Inferred from mutant phenotype
25605331 GOA
involved in negative regulation of mitochondrial fusion IMP
IMP: Inferred from mutant phenotype
20038677 GOA
involved in positive regulation of apoptotic process IDA
IDA: Inferred from direct assay
25275009 GOA
involved in protein quality control for misfolded or incompletely synthesized proteins IMP
IMP: Inferred from mutant phenotype
20038677 GOA
involved in regulation of cristae formation IDA
IDA: Inferred from direct assay
25275009 GOA
Cellular Component GO Annotation Evidence Reference Source
located in mitochondrial inner membrane IDA
IDA: Inferred from direct assay
32132707 GOA
is active in mitochondrial intermembrane space IDA
IDA: Inferred from direct assay
32132706 GOA
located in mitochondrial membrane IDA
IDA: Inferred from direct assay
20038677 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

OMA1 Protein Structure

Peptidase_M48

Peptidase_M48: Peptidase family M48 (284 - 447)

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

metalloendopeptidase OMA1, mitochondrial

OMA1 homolog, zinc metallopeptidase

Recombinant OMA1 Proteins

Cat. No. Product Name Accession Purity
HY-P72010 OMA1 Protein, Human (Cell-Free, His-SUMO) Q96E52-1 (H14-S524) ≥95%

Related Diseases

Diseases Alias
Spinocerebellar Ataxia 28

Spinocerebellar Ataxia Type 28

SCA28

Ataxia, Spinocerebellar, Type 28
3-Methylglutaconic Aciduria, Type Iii

Optic Atrophy

3-Methylglutaconic Aciduria Type 3

Costeff Syndrome

Mga3

Costeff Optic Atrophy Syndrome

Optic Atrophy Plus Syndrome

Infantile Optic Atrophy With Chorea And Spastic Paraplegia

3-Methylglutaconic Aciduria Type Iii

Autosomal Recessive Optic Atrophy Plus Syndrome

Autosomal Recessive Optic Atrophy Type 3

Opa3 Defect

MGCA3

Mga, Type Iii

Iraqi Jewish Optic Atrophy Plus

Mga Type Iii

Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia

Iraqi-Jewish 'Optic Atrophy Plus'

Optic Atrophy 3, Autosomal Recessive

Opa3, Autosomal Recessive

Opa3-Related 3-Methylglutaconic Aciduria

Iraqi-Jewish Optic Atrophy Plus

Atrophy Of Optic Disc

3-Alpha Methylglutaconic Aciduria Type Iii

Optic Atrophy 3

Optic Atrophy Infantile With Chorea And Spastic Paraplegia

Autosomal Recessive Opa3

Autosomal Recessive Optic Atrophy 3

3-Methylglutaconic Aciduria 3

3-Alpha-Methylglutaconic Aciduria Type 3

Optic Atrophy 3 Autosomal Recessive

Atrophy, Optic

Atrophy, Optic, Plus Syndrome

Optic Nerve Atrophy

Primary Optic Atrophy

Oa - [Optic Atrophy]

Second Cranial Nerve Atrophy

Second Cranium Nerve Atrophy
Behr Syndrome

BEHRS

Abortive Cerebellar Ataxia

Optic Atrophy, Infantile Hereditary, With Neurologic Abnormalities

Optic Atrophy, Infantile Hereditary, Behr Complicated Form Of

Optic Atrophy In Early Childhood, Associated With Ataxia, Spasticity, Mental Retardation, And Posterior Column Sensory Loss

Obsolete: Behr Syndrome

Optic Atrophy In Early Childhood, Associated With Ataxia, Spasticity, Intellectual Disability, And Posterior Column Sensory Loss

Infantile Hereditary Optic Atrophy With Neurologic Abnormalities
Optic Atrophy 7 With Or Without Auditory Neuropathy

Optic Atrophy 7

OPA7

Autosomal Recessive Optic Atrophy, Opa7 Type

Optic Atrophy-7

Atrophy, Optic, Type 7, With/Without Auditory Neuropathy
Combined Oxidative Phosphorylation Deficiency 33

COXPD33
Optic Atrophy 11

OPA11

Atrophy, Optic, Type 11
Optic Nerve Disease

Optic Neuropathy

Disorder Of The Second Nerve

Optic Nerve Disorder

Optic Nerve

Abnormality Of The Optic Nerve

Optic Nerve Disorders

Neuropathy, Optic

Disorder Of The Optic Nerve
Spastic Ataxia

Spax

Ataxia, Spastic
Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia
Dilated Cardiomyopathy

Familial Dilated Cardiomyopathy

Primary Dilated Cardiomyopathy

Idiopathic Dilated Cardiomyopathy

Congestive Cardiomyopathy

Idiopathic Dilation Cardiomyopathy

Primary Familial Dilated Cardiomyopathy

Cardiomyopathy, Dilated

DCM

Cardiomyopathy, Familial Dilated

Dilated Cardiomyopathy, Familial

Hypokinetic Dilated Cardiomyopathy, Familial

Familial Idiopathic Cardiomyopathy

Fdc

Cardiomyopathy, Familial Idiopathic

Idiopathic Cardiomegaly

Dilated Congestive Cardiomyopathy

Chronic Dilated Cardiomyopathy

Ccm - [Congestive Cardiomyopathy]

Cocm - [Congestive Cardiomyopathy]

Dcm - [Dilated Cardiomyopathy]

Dilated-Hypokinetic Cardiomyopathy

Congestive Idiopathic Cardiomyopathy

Primary Idiopathic Dilated Cardiomyopathy
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS09781 OMA1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus OMA1 RGD RGD:1304821
Bos taurus OMA1 VGNC VGNC:32428
Macaca mulatta OMA1 VGNC VGNC:75485
Canis familiaris OMA1 VGNC VGNC:44121
Mus musculus OMA1 MGD MGI:1914263
Felis catus OMA1 VGNC VGNC:63967
Others OMA1 NCBI