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

NEPRO - nucleolus and neural progenitor protein Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as ANXD3; NET17; C3orf17

Gene ID: 25871 | Gene type: protein coding

About 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.

Summary

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 Products(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 Protein Structure

DUF4477

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

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  • 567 a.a.
Protein Preferred Names Protein Names

nucleolus and neural progenitor protein

protein nepro homolog

Related Diseases

Diseases Alias
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
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
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS09210 NEPRO Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source 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