Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Rs6313> ?p ?o }
Showing triples 1 to 81 of
81
with 100 triples per page.
- Rs6313 abstract "In genetics, rs6313 also called T102C or C102T is a gene variation—a single nucleotide polymorphism (SNP)—in the human HTR2A gene that codes for the 5-HT2A receptor.The SNP is a synonymous substitution located in exon 1 of the gene where it is involved in coding the 34th amino acid as serine.As 5-HT2A is a neuroreceptor the SNP has been investigated in connection with brain functions and neuropsychiatric disorders, and it is perhaps the most investigated SNP for its gene.Two other SNPs in HTR2A have also received much attention: rs6311 and His452Tyr (rs6314).The T102C polymorphism has been shown to be in complete linkage disequilibrium with the rs6311 (A-1438G).A less well investigated SNP of this gene is rs7997012.Meta-analyses seem to indicate that the SNP is not directly associated with schizophrenia,not with Alzheimer's Disease,and two initial studies seem to indicate that it is not associated with Parkinson's Disease.There have been multiple studies of the effect of this SNP on clozapine treatment response in schizophrenia.A meta-analysis published in 1998 found an association.".
- Rs6313 wikiPageID "17808584".
- Rs6313 wikiPageLength "9611".
- Rs6313 wikiPageOutDegree "36".
- Rs6313 wikiPageRevisionID "679037128".
- Rs6313 wikiPageWikiLink 5-HT2A.
- Rs6313 wikiPageWikiLink 5-HT2A_receptor.
- Rs6313 wikiPageWikiLink Allele.
- Rs6313 wikiPageWikiLink Alzheimers_Disease.
- Rs6313 wikiPageWikiLink Alzheimers_disease.
- Rs6313 wikiPageWikiLink Amino_acid.
- Rs6313 wikiPageWikiLink Borderline_personality_disorder.
- Rs6313 wikiPageWikiLink Brain.
- Rs6313 wikiPageWikiLink Brain_function.
- Rs6313 wikiPageWikiLink Category:Single-nucleotide_polymorphisms.
- Rs6313 wikiPageWikiLink Clozapine.
- Rs6313 wikiPageWikiLink Endophenotype.
- Rs6313 wikiPageWikiLink Extraversion.
- Rs6313 wikiPageWikiLink Extraversion_and_introversion.
- Rs6313 wikiPageWikiLink Gene.
- Rs6313 wikiPageWikiLink Genetics.
- Rs6313 wikiPageWikiLink HTR2A.
- Rs6313 wikiPageWikiLink Hallucination.
- Rs6313 wikiPageWikiLink Hallucinations.
- Rs6313 wikiPageWikiLink His452Tyr.
- Rs6313 wikiPageWikiLink Late-onset_Alzheimers_Disease.
- Rs6313 wikiPageWikiLink Linkage_disequilibrium.
- Rs6313 wikiPageWikiLink Mental_disorder.
- Rs6313 wikiPageWikiLink Meta-analyses.
- Rs6313 wikiPageWikiLink Meta-analysis.
- Rs6313 wikiPageWikiLink Mood_disorder.
- Rs6313 wikiPageWikiLink Neuropsychiatric_disorder.
- Rs6313 wikiPageWikiLink Neuroreceptor.
- Rs6313 wikiPageWikiLink Neurotransmitter_receptor.
- Rs6313 wikiPageWikiLink Novelty_seeking.
- Rs6313 wikiPageWikiLink Parkinsons_Disease.
- Rs6313 wikiPageWikiLink Parkinsons_disease.
- Rs6313 wikiPageWikiLink Personality_traits.
- Rs6313 wikiPageWikiLink Phenotype.
- Rs6313 wikiPageWikiLink Phenotypes.
- Rs6313 wikiPageWikiLink Receptor_(biochemistry).
- Rs6313 wikiPageWikiLink Receptor_(biology).
- Rs6313 wikiPageWikiLink Reward_dependence.
- Rs6313 wikiPageWikiLink Rheumatoid_arthritis.
- Rs6313 wikiPageWikiLink Rs6311.
- Rs6313 wikiPageWikiLink Rs6314.
- Rs6313 wikiPageWikiLink Rs7997012.
- Rs6313 wikiPageWikiLink Schizophrenia.
- Rs6313 wikiPageWikiLink Serine.
- Rs6313 wikiPageWikiLink Single-nucleotide_polymorphism.
- Rs6313 wikiPageWikiLink Single_nucleotide_polymorphism.
- Rs6313 wikiPageWikiLink Synonymous_substitution.
- Rs6313 wikiPageWikiLink Trait_theory.
- Rs6313 wikiPageWikiLink Treatment_response.
- Rs6313 wikiPageWikiLinkText "rs6313".
- Rs6313 alfred "SI000324J".
- Rs6313 alzgeneGeneid "218".
- Rs6313 alzgenePolyid "564".
- Rs6313 chromosome "13".
- Rs6313 gene "HTR2A".
- Rs6313 hasPhotoCollection Rs6313.
- Rs6313 name "102".
- Rs6313 name "C102T".
- Rs6313 name "T102C".
- Rs6313 region "Exon 1".
- Rs6313 rsid "6313".
- Rs6313 szgeneGeneid "293".
- Rs6313 szgenePolyid "1862".
- Rs6313 wikiPageUsesTemplate Template:Genetics-stub.
- Rs6313 wikiPageUsesTemplate Template:Infobox_single_nucleotide_polymorphism.
- Rs6313 wikiPageUsesTemplate Template:Reflist.
- Rs6313 subject Category:Single-nucleotide_polymorphisms.
- Rs6313 hypernym u2014.
- Rs6313 type Person.
- Rs6313 comment "In genetics, rs6313 also called T102C or C102T is a gene variation—a single nucleotide polymorphism (SNP)—in the human HTR2A gene that codes for the 5-HT2A receptor.The SNP is a synonymous substitution located in exon 1 of the gene where it is involved in coding the 34th amino acid as serine.As 5-HT2A is a neuroreceptor the SNP has been investigated in connection with brain functions and neuropsychiatric disorders, and it is perhaps the most investigated SNP for its gene.Two other SNPs in HTR2A have also received much attention: rs6311 and His452Tyr (rs6314).The T102C polymorphism has been shown to be in complete linkage disequilibrium with the rs6311 (A-1438G).A less well investigated SNP of this gene is rs7997012.Meta-analyses seem to indicate that the SNP is not directly associated with schizophrenia,not with Alzheimer's Disease,and two initial studies seem to indicate that it is not associated with Parkinson's Disease.There have been multiple studies of the effect of this SNP on clozapine treatment response in schizophrenia.A meta-analysis published in 1998 found an association.".
- Rs6313 label "Rs6313".
- Rs6313 sameAs m.047g0bd.
- Rs6313 sameAs Q7375577.
- Rs6313 sameAs Q7375577.
- Rs6313 wasDerivedFrom Rs6313?oldid=679037128.
- Rs6313 isPrimaryTopicOf Rs6313.