NUDT13 - nudix hydrolase 13 Gene

Homo sapiens

Gene ID: 25961 | Gene type: protein coding

About NUDT13

Cytogenetic location: 10q22.2 Genomic coordinates (GRCh38): 10:73,110,455-73,131,823 (from NCBI)

This gene has 8 transcripts (splice variants) and 191 orthologues. Ubiquitous expression in testis (RPKM 2.0), skin (RPKM 1.9) and 25 other tissues.

Summary

Predicted to enable NADH pyrophosphatase activity. Predicted to be involved in NADH metabolic process and NADP catabolic process. Predicted to be located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

NUDT13 Products(6)

mRNA	Protein	Name
NM_001283014.2	NP_001269943.1	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform b
NM_001283015.2	NP_001269944.1	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform c
NM_001283016.2	NP_001269945.1	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform d
NM_001283017.2	NP_001269946.1	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform e
NM_001283019.2	NP_001269948.1	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform e
NM_015901.6	NP_056985.3	NAD(P)H pyrophosphatase NUDT13, mitochondrial isoform a

NUDT13 Protein Structure

NUDIX-like

zf-NADH-PPase

NUDIX

0
100
200
300
352 a.a.

Protein Preferred Names

Protein Names

NAD(P)H pyrophosphatase NUDT13, mitochondrial

nucleoside diphosphate-linked moiety X motif 13

Related Diseases

Diseases

Alias

Developmental And Epileptic Encephalopathy 5

Epileptic Encephalopathy, Early Infantile, 5	DEE5
Eiee5	Developmental And Epileptic Encephalopathy, 5
Early Infantile Epileptic Encephalopathy 5	Encephalopathy, Epileptic, Early Infantile, Type 5

Developmental And Epileptic Encephalopathy 4

DEE4	Epileptic Encephalopathy, Early Infantile, 4
Eiee4	Early Infantile Epileptic Encephalopathy 4
Stxbp1-Related Early-Onset Encephalopathy	Early Myoclonic Encephalopathy
Developmental And Epileptic Encephalopathy, 4	Stxbp1 Disorders
Stxbp1 Encephalopathy	Developmental And Epileptic Encephalopathy, Type 4
Early-Infantile Epileptic Encephalopathy 4	Stxbp1 Encephalopathy With Epilepsy
Stxbp1 Epileptic Encephalopathy	Stxbp1-Related Developmental And Epileptic Encephalopathy
Stxbp1-Related Epileptic Encephalopathy	Eme
Neonatal Epilepsy With Suppression-Burst Pattern	Encephalopathy, Epileptic, Early Infantile, Type 4

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-RS09663	NUDT13 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	NUDT13	RGD	RGD:1592767
Bos taurus	NUDT13	VGNC	VGNC:32327
Canis familiaris	NUDT13	VGNC	VGNC:44026
Macaca mulatta	NUDT13	VGNC	VGNC:75435
Mus musculus	NUDT13	MGD	MGI:1914975
Felis catus	NUDT13	VGNC	VGNC:63913

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