NUDT13 - nudix hydrolase 13 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 25961

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

NUDIX-like: NADH pyrophosphatase-like rudimentary NUDIX domain (48 - 162)

zf-NADH-PPase

zf-NADH-PPase: NADH pyrophosphatase zinc ribbon domain (165 - 195)

NUDIX

NUDIX: NUDIX domain (201 - 311)

  • 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

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
Others NUDT13 NCBI