ZDHHC8 is a putative palmitoyltransferase enzyme containing a DHHC domain that in humans is encoded by the ZDHHC8gene.[1][2][3]
References
↑Nagase T, Ishikawa K, Kikuno R, Hirosawa M, Nomura N, Ohara O (Jan 2000). "Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Res. 6 (5): 337–45. doi:10.1093/dnares/6.5.337. PMID10574462.
↑Mukai J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M, Gogos JA (Jun 2004). "Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia". Nat Genet. 36 (7): 725–31. doi:10.1038/ng1375. PMID15184899.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID14702039.
Chen WY, Shi YY, Zheng YL, et al. (2005). "Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8". Hum. Mol. Genet. 13 (23): 2991–5. doi:10.1093/hmg/ddh322. PMID15489219.
Saito S, Ikeda M, Iwata N, et al. (2005). "No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population". Neurosci. Lett. 374 (1): 21–4. doi:10.1016/j.neulet.2004.10.015. PMID15631889.
Glaser B, Schumacher J, Williams HJ, et al. (2005). "No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples". Biol. Psychiatry. 58 (1): 78–80. doi:10.1016/j.biopsych.2005.03.017. PMID15992527.
Otani K, Ujike H, Tanaka Y, et al. (2006). "The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia". Neurosci. Lett. 390 (3): 166–70. doi:10.1016/j.neulet.2005.08.019. PMID16150541.
Demily C, Legallic S, Bou J, et al. (2007). "ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia". Psychiatr. Genet. 17 (5): 311–2. doi:10.1097/YPG.0b013e328133f369. PMID17728672.