Entry - *609233 - NUDIX HYDROLASE 13; NUDT13 - OMIM

 
 
* 609233

NUDIX HYDROLASE 13; NUDT13


Alternative titles; symbols

NUCLEOSIDE DIPHOSPHATE-LINKED MOIETY X MOTIF 13
NUDIX MOTIF 13


HGNC Approved Gene Symbol: NUDT13

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


TEXT

▼ Cloning and Expression

By database analysis, Abdelraheim et al. (2003) identified NUDT13, which encodes a mitochondrial NADH diphosphatase.


▼ Mapping

By genomic sequence analysis, Abdelraheim et al. (2003) mapped the NUDT13 gene to chromosome 10q22.3.


▼ REFERENCES

  1. Abdelraheim, S. R., Spiller, D. G., McLennan, A. G. Mammalian NADH diphosphatases of the Nudix family: cloning and characterization of the human peroxisomal NUDT12 protein. Biochem. J. 374: 329-335, 2003. [PubMed: 12790796, related citations] [Full Text]


Creation Date:
Patricia A. Hartz : 3/2/2005
Edit History:
carol : 01/09/2017
mgross : 03/03/2005

* 609233

NUDIX HYDROLASE 13; NUDT13


Alternative titles; symbols

NUCLEOSIDE DIPHOSPHATE-LINKED MOIETY X MOTIF 13
NUDIX MOTIF 13


HGNC Approved Gene Symbol: NUDT13

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


TEXT

Cloning and Expression

By database analysis, Abdelraheim et al. (2003) identified NUDT13, which encodes a mitochondrial NADH diphosphatase.


Mapping

By genomic sequence analysis, Abdelraheim et al. (2003) mapped the NUDT13 gene to chromosome 10q22.3.


REFERENCES

  1. Abdelraheim, S. R., Spiller, D. G., McLennan, A. G. Mammalian NADH diphosphatases of the Nudix family: cloning and characterization of the human peroxisomal NUDT12 protein. Biochem. J. 374: 329-335, 2003. [PubMed: 12790796] [Full Text: https://doi.org/10.1042/BJ20030441]


Creation Date:
Patricia A. Hartz : 3/2/2005

Edit History:
carol : 01/09/2017
mgross : 03/03/2005



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: June 8, 2024