METTL21A, methyltransferase like 21A, 151194

N. diseases: 4; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4234080
rs4234080
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs4234080
rs4234080
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs4234080
rs4234080
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic
0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs4234080
rs4234080
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs6785
rs6785
Entrez Id: 1385;151194
Gene Symbol: CREB1;METTL21A
CREB1;METTL21A
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia
0.010 GeneticVariation BEFREE In the present study, we further expanded our analyses of rs2709370 and rs6785 in multiple BPD, SCZ and MDD data sets, including the published Psychiatric Genomics Consortium (PGC) genome-wide association study, the samples used in our previous CREB1 study, and six additional cohorts (three new BPD samples, two new SCZ samples and one new MDD sample). 29158582 2018
dbSNP: rs6785
rs6785
Entrez Id: 1385;151194
Gene Symbol: CREB1;METTL21A
CREB1;METTL21A
CUI: C0006012
Disease:
Borderline Personality Disorder
0.010 GeneticVariation BEFREE In the present study, we further expanded our analyses of rs2709370 and rs6785 in multiple BPD, SCZ and MDD data sets, including the published Psychiatric Genomics Consortium (PGC) genome-wide association study, the samples used in our previous CREB1 study, and six additional cohorts (three new BPD samples, two new SCZ samples and one new MDD sample). 29158582 2018
dbSNP: rs6785
rs6785
Entrez Id: 1385;151194
Gene Symbol: CREB1;METTL21A
CREB1;METTL21A
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE Although the associations of both CREB1 SNPs with each illness were not replicated in the new cohorts (BPD analysis in 871 cases and 1089 controls (rs2709370, P=0.0611; rs6785, P=0.0544); SCZ analysis in 1273 cases and 1072 controls (rs2709370, P=0.230; rs6785, P=0.661); and MDD analysis in 129 cases and 100 controls (rs2709370, P=0.114; rs6785, P=0.188)), an overall meta-analysis of all included samples suggested that both SNPs were significantly associated with increased risk of BPD (11 105 cases and 51 331 controls; rs2709370, P=2.33 × 10<sup>-4</sup>; rs6785, P=6.33 × 10<sup>-5</sup>), SCZ (34 913 cases and 44 528 controls; rs2709370, P=3.96 × 10<sup>-5</sup>; rs6785, P=2.44 × 10<sup>-5</sup>) and MDD (9369 cases and 9619 controls; rs2709370, P=0.0144; rs6785, P=0.0314), with the same direction of allelic effects across diagnostic categories. 29158582 2018
dbSNP: rs6785
rs6785
Entrez Id: 1385;151194
Gene Symbol: CREB1;METTL21A
CREB1;METTL21A
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE Although the associations of both CREB1 SNPs with each illness were not replicated in the new cohorts (BPD analysis in 871 cases and 1089 controls (rs2709370, P=0.0611; rs6785, P=0.0544); SCZ analysis in 1273 cases and 1072 controls (rs2709370, P=0.230; rs6785, P=0.661); and MDD analysis in 129 cases and 100 controls (rs2709370, P=0.114; rs6785, P=0.188)), an overall meta-analysis of all included samples suggested that both SNPs were significantly associated with increased risk of BPD (11 105 cases and 51 331 controls; rs2709370, P=2.33 × 10<sup>-4</sup>; rs6785, P=6.33 × 10<sup>-5</sup>), SCZ (34 913 cases and 44 528 controls; rs2709370, P=3.96 × 10<sup>-5</sup>; rs6785, P=2.44 × 10<sup>-5</sup>) and MDD (9369 cases and 9619 controls; rs2709370, P=0.0144; rs6785, P=0.0314), with the same direction of allelic effects across diagnostic categories. 29158582 2018
dbSNP: rs2551941
rs2551941
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE Individuals carrying the T- allele of rs5443 (CC), A- allele of rs2253206 (GG), T- allele of rs2551941 (AA), C- allele of rs6740584 (TT) or G- allele of rs11904814 (TT) conferred susceptibility to MD in subjects only exposed to high-negative life events. 28225778 2017
dbSNP: rs2551941
rs2551941
Entrez Id: 151194
Gene Symbol: METTL21A
METTL21A
CUI: C0041696
Disease:
Unipolar Depression
0.010 GeneticVariation BEFREE Individuals carrying the T- allele of rs5443 (CC), A- allele of rs2253206 (GG), T- allele of rs2551941 (AA), C- allele of rs6740584 (TT) or G- allele of rs11904814 (TT) conferred susceptibility to MD in subjects only exposed to high-negative life events. 28225778 2017