2. Gene
  3. NEPRO - nucleolus and neural progenitor protein Gene

NEPRO - nucleolus and neural progenitor protein Gene

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

中文名称：核仁和神经祖细胞蛋白

种属: Homo sapiens

同用名: ANXD3; NET17; C3orf17

基因 ID: 25871 | 基因类型: protein coding

关于 NEPRO

Cytogenetic location: 3q13.2 Genomic coordinates (GRCh38): 3:113,002,444-113,019,671 (from NCBI)

This gene has 24 transcripts (splice variants), 183 orthologues and is associated with 2 phenotypes. Ubiquitous expression in thyroid (RPKM 9.6), lymph node (RPKM 9.2) and 25 other tissues.

功能概要

预计参与神经元分化的负调控和 Notch 信号通路的正调控。预测位于核仁中。预计活跃于核心。涉及 anauxetic 发育不良 3。[由基因组资源联盟提供，2022 年 4 月]

Predicted to be involved in negative regulation of neuron differentiation and positive regulation of Notch signaling pathway. Predicted to be located in nucleolus. Predicted to be active in nucleus. Implicated in anauxetic dysplasia 3. [provided by Alliance of Genome Resources, Apr 2022]

NEPRO 基因产物(7)

mRNA Protein Name
NM_001319109.2 NP_001306038.1 nucleolus and neural progenitor protein isoform d
NM_001319110.2 NP_001306039.1 nucleolus and neural progenitor protein isoform e
NM_001319111.2 NP_001306040.1 nucleolus and neural progenitor protein isoform f
NM_001319112.2 NP_001306041.1 nucleolus and neural progenitor protein isoform g
NM_001319114.2 NP_001306043.1 nucleolus and neural progenitor protein isoform b
NM_001319115.2 NP_001306044.1 nucleolus and neural progenitor protein isoform c
NM_015412.4 NP_056227.2 nucleolus and neural progenitor protein isoform a

NEPRO 蛋白结构

DUF4477

DUF4477: Domain of unknown function (DUF4477) (12 - 202)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 567 a.a.
蛋白主名 其他名称

nucleolus and neural progenitor protein

protein nepro homolog

关联疾病

疾病名称 别名
Anauxetic Dysplasia 3

ANXD3
Anauxetic Dysplasia 1

Anauxetic Dysplasia

Spondylometaepiphyseal Dysplasia, Menger Type

Spondylometaepiphyseal Dysplasia, Anauxetic Type

Spondyloepimetaphyseal Dysplasia, Anauxetic Type

ANXD1

Anxd

Spondylometaepiphyseal Dysplasia Anauxetic Type

Spondylometaepiphyseal Dysplasia Menger Type

Ad

Spondyloepimetaphyseal Dysplasia, Menger Type

Dysplasia, Anauxetic, Type 1
Anauxetic Dysplasia 2

ANXD2
Alcohol-Related Neurodevelopmental Disorder

Static Encephalopathy

Arnd

Encephalopathy, Static

Alcohol Related Neurodevelopmental Disorder
Brachydactyly
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-RS09210 NEPRO Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Canis familiaris NEPRO VGNC VGNC:43746
Mus musculus NEPRO MGD MGI:2384836
Bos taurus NEPRO VGNC VGNC:32008
Macaca mulatta NEPRO VGNC VGNC:75244
Felis catus NEPRO VGNC VGNC:63778
Rattus norvegicus NEPRO RGD RGD:1311458
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