List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Glycemic traits. The EFO term type II diabetes mellitus was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
MJ Go, JY Hwang, YJ Kim, J Hee Oh, YJ Kim, S Heon Kwak, K Soo Park, J Lee, BJ Kim, BG Han, MC Cho, YS Cho, JY Lee
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Gamma glutamyl transpeptidase. The EFO term serum gamma-glutamyl transferase measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
GWAS: high density lipoprotein cholesterol measurement
Description:
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was HDL cholesterol. The EFO term high density lipoprotein cholesterol measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
GNF2_MYL2
Neighborhood of MYL2
c4 - Computational genesets defined by mining large collections of cancer-oriented microarray data.
Molecular Signatures Database (MSigDB) Geneset. This geneset was imported from one of the MSigDB collections.
gene2msig v. 0.1.0
Last updated 2015.08.31
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Body mass index. The EFO term body mass index was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
W Wen, W Zheng, Y Okada, F Takeuchi, Y Tabara, JY Hwang, R Dorajoo, H Li, FJ Tsai, X Yang, J He, Y Wu, M He, Y Zhang, J Liang, X Guo, WH Sheu, R Delahanty, X Guo, M Kubo, K Yamamoto, T Ohkubo, MJ Go, JJ Liu, W Gan, CC Chen, Y Gao, S Li, NR Lee, C Wu, X Zhou, H Song, J Yao, IT Lee, J Long, T Tsunoda, K Akiyama, N Takashima, YS Cho, RT Ong, L Lu, CH Chen, A Tan, TK Rice, LS Adair, L Gui, M Allison, WJ Lee, Q Cai, M Isomura, S Umemura, YJ Kim, M Seielstad, J Hixson, YB Xiang, M Isono, BJ Kim, X Sim, W Lu, T Nabika, J Lee, WY Lim, YT Gao, R Takayanagi, DH Kang, TY Wong, CA Hsiung, IC Wu, JM Juang, J Shi, BY Choi, T Aung, F Hu, MK Kim, WY Lim, TD Wang, MH Shin, J Lee, BT Ji, YH Lee, TL Young, DH Shin, BY Chun, MC Cho, BG Han, CM Hwu, TL Assimes, D Absher, X Yan, E Kim, JZ Kuo, S Kwon, KD Taylor, YD Chen, JI Rotter, L Qi, D Zhu, T Wu, KL Mohlke, D Gu, Z Mo, JY Wu, X Lin, T Miki, ES Tai, JY Lee, N Kato, XO Shu, T Tanaka
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Metabolite levels. The EFO term uric acid measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Metabolite levels. The EFO term serum albumin measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Metabolite levels. The EFO term fasting blood glucose measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Triglycerides. The EFO term triglyceride measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Metabolite levels. The EFO term serum alanine aminotransferase measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
GWAS: low density lipoprotein cholesterol measurement
Description:
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Metabolite levels. The EFO term low density lipoprotein cholesterol measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
YJ Kim, MJ Go, C Hu, CB Hong, YK Kim, JY Lee, JY Hwang, JH Oh, DJ Kim, NH Kim, S Kim, EJ Hong, JH Kim, H Min, Y Kim, R Zhang, W Jia, Y Okada, A Takahashi, M Kubo, T Tanaka, N Kamatani, K Matsuda, T Park, B Oh, K Kimm, D Kang, C Shin, NH Cho, HL Kim, BG Han, JY Lee, YS Cho
Whole Brain Gene Expression Correlates for MDMA_ACT_MDA_1 measured in BXD RI Males obtained using INIA Brain mRNA M430 (Jun06) RMA. The MDMA_ACT_MDA_1 measures Locomotor response of 10 mg/kg MDMA injected on Day 2 under the domain MDMA. The correlates were thresholded at a p-value of less than 0.001.
Authors:
Philip VM, Duvvuru S, Gomero B, Ansah TA, Blaha CD, Cook MN, Hamre KM, Lariviere WR, Matthews DB, Mittleman G, Goldowitz D, Chesler EJ
QTL for cocaine related behavior on Chr5 at D5Mit7 (103.64 Mbp , Build 37)
Description:
cocaine related behavior spans 78.64 - 128.64 Mbp (NCBI Build 37) on Chr5. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for differences in cocaine responsiveness on Chr5 at Cyp3 (108.78 Mbp , Build 37)
Description:
differences in cocaine responsiveness spans 83.78 - 133.78 Mbp (NCBI Build 37) on Chr5. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for METH responses for chewing on Chr5 at D5Mit10 (111.96 Mbp , Build 37)
Description:
METH responses for chewing spans 86.96 - 136.96 Mbp (NCBI Build 37) on Chr5. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for METH responses for climbing on Chr5 at D5Byu4 (129.78 Mbp , Build 37)
Description:
METH responses for climbing spans 104.78 - 154.78 Mbp (NCBI Build 37) on Chr5. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for METH responses for climbing on Chr5 at Ache (142.47 Mbp , Build 37)
Description:
METH responses for climbing spans 117.47 - 167.47 Mbp (NCBI Build 37) on Chr5. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
Chronic ethanol - Ethanol vs. Control DNA microarray Change in gene expression - Class II Alcoholics were classified based on the quantity of alcohol consumed, according to the National Health and Medical Research Council (NHMRC) (>80 g of alcohol per day), instead of the criteria established by the American Psychiatric Association (DSM-IV) or the World Health Organization (ICD-10). Many alcoholic patients in this study consumed significantly more than 80 g / day for most of their adult life. Cerebral atrophy was observed in three alcoholic cases. All alcoholic cases included in our Axon GenePix 4.0 software; partial least squares (PLS) statistical procedure; linear discriminant analysis (LDA) procedure for prediction analysis. PLS and LDA analysis were performed using in JMP IN software; principal component analysis (PCA) used STATISTICA software. Results reflect the combined dataset: Class I genes were qualitatively different, that is, they were predominantly detected in one group but not the other. They represent those that were more likely turned off or turned on as a result of alcohol abuse. Class II genes were consistently detected in both groups. They represent consistently expressed genes for which quantitative differences in expression could be determined. (NIF Method ID 157)
Genes associated with Oikopleura dioica that interact with the MeSH term 'Clofibrate' (D002994). Incorporates data from 27 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Oryctolagus cuniculus that interact with the MeSH term 'Ionomycin' (D015759). Incorporates data from 6 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'Smoke' (D012906). Incorporates data from 54 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
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