NEPRO - nucleolus and neural progenitor protein Gene

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

0
100
200
300
400
500
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		/	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

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