2. Gene
  3. NOL10 - nucleolar protein 10 Gene

NOL10 - nucleolar protein 10 Gene

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

中文名称：核仁蛋白 10

种属: Homo sapiens

同用名: PQBP5

基因 ID: 79954 | 基因类型: protein coding

关于 NOL10

Cytogenetic location: 2p25.1 Genomic coordinates (GRCh38): 2:10,570,754-10,689,975 (from NCBI)

This gene has 22 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in testis (RPKM 4.5), adrenal (RPKM 4.0) and 25 other tissues.

功能概要

启用 RNA 结合活性。预测参与来自三顺反子 rRNA 转录物 (SSU-rRNA、5.8S rRNA、LSU-rRNA) 的 SSU-rRNA 的成熟。位于核仁。 [由基因组资源联盟提供，2022 年 4 月]

Enables RNA binding activity. Predicted to be involved in maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Located in nucleolus. [provided by Alliance of Genome Resources, Apr 2022]

NOL10 基因产物(3)

mRNA Protein Name
NM_001261392.2 NP_001248321.1 nucleolar protein 10 isoform 2
NM_001261394.2 NP_001248323.1 nucleolar protein 10 isoform 3
NM_024894.4 NP_079170.2 nucleolar protein 10 isoform 1

NOL10 蛋白结构

NUC153

NUC153: NUC153 domain (482 - 508)

  • 0
  • 200
  • 400
  • 600
  • 688 a.a.
蛋白主名 其他名称

nucleolar protein 10

H_NH0074G24.1

关联疾病

疾病名称 别名
Renpenning Syndrome 1

Renpenning Syndrome

Golabi-Ito-Hall Syndrome

Mrxs3

Mrxs8

X-Linked Intellectual Disability Due To Pqbp1 Mutations

RENS1

Sutherland-Haan X-Linked Mental Retardation Syndrome

Shs

Mrx55

X-Linked Intellectual Disability, Renpenning Type

Sutherland-Haan Syndrome

Mental Retardation, X-Linked, Renpenning Type

Mental Retardation, X-Linked, With Spastic Diplegia

Mental Retardation, X-Linked, Syndromic 3

Mental Retardation, X-Linked, Syndromic 8

Mental Retardation, X-Linked 55

Syndromic X-Linked Mental Retardation 8

X-Linked Mental Retardation Renpenning Type

X-Linked Mental Retardation With Spastic Diplegia

Sutherland-Haan X-Linked Intellectual Disability Syndrome

X-Linked Intellectual Disability With Spastic Diplegia

Hamel Cerebropalatocardiac Syndrome

Porteous Syndrome

X-Linked Intellectual Deficit Due To Pqbp1 Mutations

X-Linked Intellectual Deficit, Renpenning Type

X-Linked Intellectual Disability, Sutherland-Haan Type

Hamel Cerebro-Palato-Cardiac Syndrome

Renpenning Syndrome, Type 1
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-RS09411 NOL10 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus NOL10 RGD RGD:1359447
Macaca mulatta NOL10 VGNC VGNC:75260
Canis familiaris NOL10 VGNC VGNC:43880
Mus musculus NOL10 MGD MGI:2684913
Bos taurus NOL10 VGNC VGNC:32154
Felis catus NOL10 VGNC VGNC:63850
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