2. Gene
  3. CCDC90B - coiled-coil domain containing 90B Gene

CCDC90B - coiled-coil domain containing 90B Gene

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

中文名称：含卷曲螺旋结构域 90B

种属: Homo sapiens

同用名: MDS011; MDS025

基因 ID: 60492 | 基因类型: protein coding

关于 CCDC90B

This gene has 19 transcripts (splice variants), 205 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 14.9), adrenal (RPKM 10.5) and 25 other tissues.

功能概要

位于线粒体中。 [由基因组资源联盟提供，2022 年 4 月]

Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

CCDC90B 基因产物(6)

mRNA Protein Name
NM_001286116.2 NP_001273045.2 coiled-coil domain-containing protein 90B, mitochondrial isoform c
NM_001286117.3 NP_001273046.1 coiled-coil domain-containing protein 90B, mitochondrial isoform c
NM_001286118.3 NP_001273047.1 coiled-coil domain-containing protein 90B, mitochondrial isoform d
NM_001286119.3 NP_001273048.1 coiled-coil domain-containing protein 90B, mitochondrial isoform d
NM_001286120.3 NP_001273049.1 coiled-coil domain-containing protein 90B, mitochondrial isoform e
NM_021825.5 NP_068597.2 coiled-coil domain-containing protein 90B, mitochondrial isoform 1 precursor

CCDC90B 蛋白结构

DUF1640

DUF1640: Protein of unknown function (DUF1640) (60 - 254)

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

coiled-coil domain-containing protein 90B, mitochondrial

关联疾病

疾病名称 别名
Oculoauricular Syndrome

OCACS

Schorderet-Munier-Franceschetti Syndrome

Microphthalmia, Microcornea, Anterior Segment Dysgenesis, Cataract, Ocular Coloboma, Retinal Pigment Epithelium Abnormalities, Rod-Cone Dystrophy, And Anomalies Of The External Ear

Oculoauricular Syndrome, Schorderet Type

Oculo-Auricular Syndrome
Osteochondrosis

Osteochondritis

Apophysitis

Epiphysitis

Osteochondritis Juvenilis

Epiphyseal Necrosis

Juvenile Osteochondrosis Of Tibial Tubercle
Epilepsy, Myoclonic Juvenile

Juvenile Myoclonic Epilepsy

Janz Syndrome

Jme

Myoclonic Epilepsy, Juvenile, Susceptibility To, 1

EJM

Myoclonic Epilepsy, Juvenile

Petit Mal, Impulsive

Myoclonic Epilepsy, Juvenile 1

Myoclonic Epilepsy, Juvenile, 1

Adolescent Myoclonic Epilepsy

Juvenile Myoclonus Epilepsy

Juvenile Myoclonic Epilepsy 1

EJM1

Petit Mal Impulsive

Susceptibility To Juvenile Myoclonic Epilepsy 1

Myoclonic Epilepsy Juvenile

Epilepsy, Myoclonic, Juvenile

Myoclonic Epilepsy Of Janz

Jme - [Juvenile Myoclonic Epilepsy]
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-RS02065 CCDC90B Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Bos taurus CCDC90B VGNC VGNC:26931
Mus musculus CCDC90B MGD MGI:1913615
Rattus norvegicus CCDC90B RGD RGD:1308637
Canis familiaris CCDC90B VGNC VGNC:38871
Macaca mulatta CCDC90B VGNC VGNC:70886
Felis catus CCDC90B VGNC VGNC:60527
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