2. Gene
  3. OXA1L - OXA1L mitochondrial inner membrane protein Gene

OXA1L - OXA1L mitochondrial inner membrane protein Gene

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

Also known as OXA1; OXA1L1

Gene ID: 5018 | Gene type: protein coding

About OXA1L

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:22,766,688-22,773,042 (from NCBI)

This gene has 12 transcripts (splice variants), 201 orthologues and 1 paralogue. Ubiquitous expression in heart (RPKM 54.4), duodenum (RPKM 53.5) and 25 other tissues.

Summary

This gene encodes an evolutionarily conserved protein that is localized to the inner mitochondrial membrane. The encoded protein is essential for the translocation of the N-terminal tail of subunit 2 of cytochrome c oxidase, and is involved in the assembly of the cytochrome c oxidase and ATPase complexes of the mitochondrial respiratory chain. [provided by RefSeq, Jul 2016]

OXA1L Products(1)

mRNA Protein Name
NM_005015.5 NP_005006.4 mitochondrial inner membrane protein OXA1L

OXA1L Protein Structure

60KD_IMP

60KD_IMP: 60Kd inner membrane protein (200 - 394)

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

mitochondrial inner membrane protein OXA1L

OXA1-like protein

Related Diseases

Diseases Alias
Mitochondrial Disease

Mitochondrial Diseases

Mitochondrial Disorder
Hyperthyroxinemia
Raynaud-Claes Syndrome

Mrx49

MRXSRC

Mental Retardation, X-Linked 49

Mrx15

Clcn4-Related X-Linked Intellectual Disability Syndrome

Mental Retardation, X-Linked 15

X-Linked Mental Retardation 15

X-Linked Mental Retardation 49

Mental Retardation, X-Linked-49
Central Corneal Ulcer
Absolute Glaucoma

Blind Hypertensive Eye

Glaucoma Absolute
Parametritis

Pelvic Cellulitis
Urinary Tract Infection

Urinary Tract Infections

Uti

Urinary Tract Infection Nos

Uti - [Urinary Tract Infection]

Uti Nos - [Urinary Tract Infection Nos]

Urosepsis Nos

E Coli Uti

E Coli Urinary Tract Infection

Escherichia Coli Uti
Analbuminemia

ANALBA

Congenital Analbuminemia

Hypoalbuminemia
Diabetes Mellitus

Diabetes
Wolf-Hirschhorn Syndrome

Pitt-Rogers-Danks Syndrome

WHS

Chromosome 4p16.3 Deletion Syndrome

Wittwer Syndrome

4p- Syndrome

Pitt Syndrome

4p Deletion Syndrome

Distal Deletion 4p

Distal Monosomy 4p

Telomeric Deletion 4p

Prds

4p Syndrome

Chromosome 4p Syndrome

Microcephaly, Iugr, Hypertelorism, Ptosis, Iris Coloboma, Hooked Nose, External Ear Dysplasia, Psychomotor Retardation

Wolf Syndrome

Chromosome 4p Deletion Syndrome

Chromosome 4p Monosomy

Del Syndrome

Monosomy 4p

Partial Monosomy 4p

Chromosome 4 Short Arm Deletion
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-RS09885 OXA1L Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus OXA1L MGD MGI:1916339
Macaca mulatta OXA1L VGNC VGNC:75729
Rattus norvegicus OXA1L RGD RGD:1585024
Canis familiaris OXA1L VGNC VGNC:44199
Bos taurus OXA1L VGNC VGNC:32507
Felis catus OXA1L VGNC VGNC:80889