2. Gene
  3. COQ10B - coenzyme Q10B Gene

COQ10B - coenzyme Q10B Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens
Gene ID: 80219 | Gene type: protein coding

About COQ10B

This gene has 4 transcripts (splice variants), 223 orthologues and 1 paralogue. Ubiquitous expression in adrenal (RPKM 15.0), bone marrow (RPKM 11.9) and 25 other tissues.

Summary

Predicted to enable ubiquinone binding activity. Predicted to be involved in cellular respiration and ubiquinone biosynthetic process. Predicted to be located in mitochondrial inner membrane. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

COQ10B Products(4)

mRNA Protein Name
NM_001320818.2 NP_001307747.1 coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform 2
NM_001320819.2 NP_001307748.1 coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform 3
NM_001320820.2 NP_001307749.1 coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform 4
NM_025147.5 NP_079423.1 coenzyme Q-binding protein COQ10 homolog B, mitochondrial isoform 1 precursor

COQ10B Protein Structure

Polyketide_cyc

Polyketide_cyc: Polyketide cyclase / dehydrase and lipid transport (85 - 213)

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

coenzyme Q-binding protein COQ10 homolog B, mitochondrial

coenzyme Q10 homolog B

Related Diseases

Diseases Alias
Combined Oxidative Phosphorylation Deficiency 7

COXPD7

Combined Oxidative Phosphorylation Defect Type 7

Severe C12orf65-Related Combined Oxidative Phosphorylation Defect

Severe C12orf65-Related Coxpd

Combined Oxidative Phosphorylation Deficiency, Type 7
Nephrotic Syndrome, Type 9

NPHS9

Nephrotic Syndrome Type 9

Nephrotic Syndrome 9
Congenital Disorder Of Glycosylation, Type Ip

CDG1P

Congenital Disorder Of Glycosylation Ip

Congenital Disorder Of Glycosylation 1p

Alg11-Cdg

Cdg-Ip

Congenital Disorder Of Glycosylation Type Ip

Cdg Syndrome Type Ip

Carbohydrate Deficient Glycoprotein Syndrome Type Ip

Congenital Disorder Of Glycosylation Type 1p

Cdgip

Cdg Ip

Glycosylation, Congenital Disorder Of, Type Ip
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-RS03037 COQ10B Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus COQ10B RGD RGD:1359509
Macaca mulatta COQ10B VGNC VGNC:71351
Canis familiaris COQ10B VGNC VGNC:57378
Mus musculus COQ10B MGD MGI:1915126
Bos taurus COQ10B VGNC VGNC:27610