2. Gene
  3. COQ10B - coenzyme Q10B Gene

COQ10B - coenzyme Q10B Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：辅酶 Q10B

种属: Homo sapiens

基因 ID: 80219 | 基因类型: protein coding

关于 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.

功能概要

预测启用泛醌结合活性。预测参与细胞呼吸和泛醌生物合成过程。预测位于线粒体内膜。预测在线粒体中活跃。 [由基因组资源联盟提供，2022 年 4 月]

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 基因产物(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 蛋白结构

Polyketide_cyc

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

  • 0
  • 100
  • 200
  • 238 a.a.
蛋白主名 其他名称

coenzyme Q-binding protein COQ10 homolog B, mitochondrial

coenzyme Q10 homolog B

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS03037 COQ10B Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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
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