GLUDP5

Glutamate dehydrogenase pseudogene 5
Identifiers
Symbols	GLUDP5 ;
Gene ontology
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Glutamate dehydrogenase pseudogene 5, also known as GLUDP5, is a human gene.

Further reading

• Meissner T, Beinbrech B, Mayatepek E (1999). "Congenital hyperinsulinism: molecular basis of a heterogeneous disease". Hum. Mutat. 13 (5): 351–61. doi:10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R. PMID 10338089.CS1 maint: Multiple names: authors list (link)
• Julliard JH, Smith EL (1979). "Partial amino acid sequence of the glutamate dehydrogenase of human liver and a revision of the sequence of the bovine enzyme". J. Biol. Chem. 254 (9): 3427–38. PMID 429360.
• Hochstrasser DF, Frutiger S, Paquet N; et al. (1993). "Human liver protein map: a reference database established by microsequencing and gel comparison". Electrophoresis. 13 (12): 992–1001. PMID 1286669.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Mavrothalassitis G, Tzimagiorgis G, Mitsialis A; et al. (1988). "Isolation and characterization of cDNA clones encoding human liver glutamate dehydrogenase: evidence for a small gene family". Proc. Natl. Acad. Sci. U.S.A. 85 (10): 3494–8. PMID 3368458.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Amuro N, Yamaura M, Goto Y, Okazaki T (1988). "Molecular cloning and nucleotide sequence of the cDNA for human liver glutamate dehydrogenase precursor". Biochem. Biophys. Res. Commun. 152 (3): 1395–400. PMID 3377777.CS1 maint: Multiple names: authors list (link)
• Nakatani Y, Schneider M, Banner C, Freese E (1988). "Complete nucleotide sequence of human glutamate dehydrogenase cDNA". Nucleic Acids Res. 16 (13): 6237. PMID 3399399.CS1 maint: Multiple names: authors list (link)
• Nakatani Y, Banner C, von Herrath M; et al. (1988). "Comparison of human brain and liver glutamate dehydrogenase cDNAS". Biochem. Biophys. Res. Commun. 149 (2): 405–10. PMID 3426581.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Banner C, Silverman S, Thomas JW; et al. (1987). "Isolation of a human brain cDNA for glutamate dehydrogenase". J. Neurochem. 49 (1): 246–52. PMID 3585334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Tzimagiorgis G, Leversha MA, Chroniary K; et al. (1993). "Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2". Hum. Genet. 91 (5): 433–8. PMID 8314555.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Goulielmos G, Angelicheva D, Kapsetaki M; et al. (1993). "A chromosome 10p11.2 Gt-dinucleotide repeat polymorphism at the GLUDP5 gene locus". Hum. Mol. Genet. 2 (8): 1328. PMID 8401522.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Michaelidis TM, Tzimagiorgis G, Moschonas NK, Papamatheakis J (1993). "The human glutamate dehydrogenase gene family: gene organization and structural characterization". Genomics. 16 (1): 150–60. doi:10.1006/geno.1993.1152. PMID 8486350.CS1 maint: Multiple names: authors list (link)
• Stanley CA, Lieu YK, Hsu BY; et al. (1998). "Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene". N. Engl. J. Med. 338 (19): 1352–7. PMID 9571255.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Miki Y, Taki T, Ohura T; et al. (2000). "Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome". J. Pediatr. 136 (1): 69–72. PMID 10636977.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Santer R, Kinner M, Passarge M; et al. (2001). "Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome". Hum. Genet. 108 (1): 66–71. PMID 11214910.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Smith TJ, Peterson PE, Schmidt T; et al. (2001). "Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation". J. Mol. Biol. 307 (2): 707–20. doi:10.1006/jmbi.2001.4499. PMID 11254391.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• MacMullen C, Fang J, Hsu BY; et al. (2001). "Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase". J. Clin. Endocrinol. Metab. 86 (4): 1782–7. PMID 11297618.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Fang J, Hsu BY, MacMullen CM; et al. (2002). "Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations". Biochem. J. 363 (Pt 1): 81–7. PMID 11903050.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Smith TJ, Schmidt T, Fang J; et al. (2002). "The structure of apo human glutamate dehydrogenase details subunit communication and allostery". J. Mol. Biol. 318 (3): 765–77. doi:10.1016/S0022-2836(02)00161-4. PMID 12054821.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Banerjee S, Schmidt T, Fang J; et al. (2003). "Structural studies on ADP activation of mammalian glutamate dehydrogenase and the evolution of regulation". Biochemistry. 42 (12): 3446–56. doi:10.1021/bi0206917. PMID 12653548.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)