COQ10B - coenzyme Q10B Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 80219

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

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 Set / 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
Others COQ10B NCBI