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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 08 Dec 2016.

Glyceronephosphate O-acyltransferase

DHAP-AT, DAP at
This gene encodes an enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in this gene are associated with rhizomelic chondrodysplasia punctata. [provided by RefSeq, Jul 2008] (from NCBI)
Papers on DHAP-AT
Impaired neurotransmission in ether lipid-deficient nerve terminals.
GeneRIF
Just et al., Heidelberg, Germany. In Hum Mol Genet, 2012
Data show that EL deficiency (DHAPAT-null) caused the reduction in synaptic respiratory activity and consequently the decrease in the ATP/ADP ratio by >20%.
Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3.
GeneRIF
Braverman et al., Montréal, Canada. In Hum Mutat, 2012
Novel mutations in GNPAT cause rhizomelic chondrodysplasia punctata (RCDP) type 2.
A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.
GeneRIF
Hwu et al., Taipei, Taiwan. In Biol Psychiatry, 2006
Chromosome 1q42.1 harbors GNPAT and DISC1 as candidate genes for schizophrenia.
Role of dihydroxyacetonephosphate acyltransferase in the biosynthesis of plasmalogens and nonether glycerolipids.
GeneRIF
Zoeller et al., Boston, United States. In J Lipid Res, 2005
peroxisomal DHAPAT is essential for the biosynthesis of plasmalogens in animal cells
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