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 Kidney function decline traits. The EFO term rapid kidney function decline 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:
M Gorski, A Tin, M Garnaas, GM McMahon, AY Chu, BO Tayo, C Pattaro, A Teumer, DI Chasman, J Chalmers, P Hamet, J Tremblay, M Woodward, T Aspelund, G Eiriksdottir, V Gudnason, TB Harris, LJ Launer, AV Smith, BD Mitchell, JR O'Connell, AR Shuldiner, J Coresh, M Li, P Freudenberger, E Hofer, H Schmidt, R Schmidt, EG Holliday, P Mitchell, JJ Wang, IH de Boer, G Li, DS Siscovick, Z Kutalik, T Corre, P Vollenweider, G Waeber, J Gupta, PA Kanetsky, SJ Hwang, M Olden, Q Yang, M de Andrade, EJ Atkinson, SL Kardia, ST Turner, JM Stafford, J Ding, Y Liu, C Barlassina, D Cusi, E Salvi, JA Staessen, PM Ridker, H Grallert, C Meisinger, M Müller-Nurasyid, BK Krämer, H Kramer, SE Rosas, IM Nolte, BW Penninx, H Snieder, M Fabiola Del Greco, A Franke, U Nöthlings, W Lieb, SJ Bakker, RT Gansevoort, P van der Harst, A Dehghan, OH Franco, A Hofman, F Rivadeneira, S Sedaghat, AG Uitterlinden, S Coassin, M Haun, B Kollerits, F Kronenberg, B Paulweber, N Aumann, K Endlich, M Pietzner, U Völker, R Rettig, V Chouraki, C Helmer, JC Lambert, M Metzger, B Stengel, T Lehtimäki, LP Lyytikäinen, O Raitakari, A Johnson, A Parsa, M Bochud, IM Heid, W Goessling, A Köttgen, WH Kao, CS Fox, CA Böger
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 Kidney function decline traits. The EFO term chronic kidney disease 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:
M Gorski, A Tin, M Garnaas, GM McMahon, AY Chu, BO Tayo, C Pattaro, A Teumer, DI Chasman, J Chalmers, P Hamet, J Tremblay, M Woodward, T Aspelund, G Eiriksdottir, V Gudnason, TB Harris, LJ Launer, AV Smith, BD Mitchell, JR O'Connell, AR Shuldiner, J Coresh, M Li, P Freudenberger, E Hofer, H Schmidt, R Schmidt, EG Holliday, P Mitchell, JJ Wang, IH de Boer, G Li, DS Siscovick, Z Kutalik, T Corre, P Vollenweider, G Waeber, J Gupta, PA Kanetsky, SJ Hwang, M Olden, Q Yang, M de Andrade, EJ Atkinson, SL Kardia, ST Turner, JM Stafford, J Ding, Y Liu, C Barlassina, D Cusi, E Salvi, JA Staessen, PM Ridker, H Grallert, C Meisinger, M Müller-Nurasyid, BK Krämer, H Kramer, SE Rosas, IM Nolte, BW Penninx, H Snieder, M Fabiola Del Greco, A Franke, U Nöthlings, W Lieb, SJ Bakker, RT Gansevoort, P van der Harst, A Dehghan, OH Franco, A Hofman, F Rivadeneira, S Sedaghat, AG Uitterlinden, S Coassin, M Haun, B Kollerits, F Kronenberg, B Paulweber, N Aumann, K Endlich, M Pietzner, U Völker, R Rettig, V Chouraki, C Helmer, JC Lambert, M Metzger, B Stengel, T Lehtimäki, LP Lyytikäinen, O Raitakari, A Johnson, A Parsa, M Bochud, IM Heid, W Goessling, A Köttgen, WH Kao, CS Fox, CA Böger
GWAS: chronic kidney disease, GFR change 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 Kidney function decline traits. The EFO term chronic kidney disease, GFR change 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:
M Gorski, A Tin, M Garnaas, GM McMahon, AY Chu, BO Tayo, C Pattaro, A Teumer, DI Chasman, J Chalmers, P Hamet, J Tremblay, M Woodward, T Aspelund, G Eiriksdottir, V Gudnason, TB Harris, LJ Launer, AV Smith, BD Mitchell, JR O'Connell, AR Shuldiner, J Coresh, M Li, P Freudenberger, E Hofer, H Schmidt, R Schmidt, EG Holliday, P Mitchell, JJ Wang, IH de Boer, G Li, DS Siscovick, Z Kutalik, T Corre, P Vollenweider, G Waeber, J Gupta, PA Kanetsky, SJ Hwang, M Olden, Q Yang, M de Andrade, EJ Atkinson, SL Kardia, ST Turner, JM Stafford, J Ding, Y Liu, C Barlassina, D Cusi, E Salvi, JA Staessen, PM Ridker, H Grallert, C Meisinger, M Müller-Nurasyid, BK Krämer, H Kramer, SE Rosas, IM Nolte, BW Penninx, H Snieder, M Fabiola Del Greco, A Franke, U Nöthlings, W Lieb, SJ Bakker, RT Gansevoort, P van der Harst, A Dehghan, OH Franco, A Hofman, F Rivadeneira, S Sedaghat, AG Uitterlinden, S Coassin, M Haun, B Kollerits, F Kronenberg, B Paulweber, N Aumann, K Endlich, M Pietzner, U Völker, R Rettig, V Chouraki, C Helmer, JC Lambert, M Metzger, B Stengel, T Lehtimäki, LP Lyytikäinen, O Raitakari, A Johnson, A Parsa, M Bochud, IM Heid, W Goessling, A Köttgen, WH Kao, CS Fox, CA Böger
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 Kidney function decline traits. The EFO term GFR change 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:
M Gorski, A Tin, M Garnaas, GM McMahon, AY Chu, BO Tayo, C Pattaro, A Teumer, DI Chasman, J Chalmers, P Hamet, J Tremblay, M Woodward, T Aspelund, G Eiriksdottir, V Gudnason, TB Harris, LJ Launer, AV Smith, BD Mitchell, JR O'Connell, AR Shuldiner, J Coresh, M Li, P Freudenberger, E Hofer, H Schmidt, R Schmidt, EG Holliday, P Mitchell, JJ Wang, IH de Boer, G Li, DS Siscovick, Z Kutalik, T Corre, P Vollenweider, G Waeber, J Gupta, PA Kanetsky, SJ Hwang, M Olden, Q Yang, M de Andrade, EJ Atkinson, SL Kardia, ST Turner, JM Stafford, J Ding, Y Liu, C Barlassina, D Cusi, E Salvi, JA Staessen, PM Ridker, H Grallert, C Meisinger, M Müller-Nurasyid, BK Krämer, H Kramer, SE Rosas, IM Nolte, BW Penninx, H Snieder, M Fabiola Del Greco, A Franke, U Nöthlings, W Lieb, SJ Bakker, RT Gansevoort, P van der Harst, A Dehghan, OH Franco, A Hofman, F Rivadeneira, S Sedaghat, AG Uitterlinden, S Coassin, M Haun, B Kollerits, F Kronenberg, B Paulweber, N Aumann, K Endlich, M Pietzner, U Völker, R Rettig, V Chouraki, C Helmer, JC Lambert, M Metzger, B Stengel, T Lehtimäki, LP Lyytikäinen, O Raitakari, A Johnson, A Parsa, M Bochud, IM Heid, W Goessling, A Köttgen, WH Kao, CS Fox, CA Böger
Hippocampus Gene Expression Correlates for ENTRIES_CLOSED measured in BXD RI Males obtained using GeneNetwork Hippocampus Consortium M430v2 (Jun06) RMA. The ENTRIES_CLOSED measures Number of entries into closed arms of plus maze under the domain Ethanol. The correlates were thresholded at a p-value of less than 0.001.
Whole Brain Gene Expression Correlates for OF_REAR_0_5 measured in BXD RI Males obtained using INIA Brain mRNA M430 (Jun06) RMA. The OF_REAR_0_5 measures Open Field - Total rears 0-5 minutes under the domain Basal Behavior. 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 METH responses for home cage activity on Chr5 at D5Ncvs56 (28.53 Mbp , Build 37)
Description:
METH responses for home cage activity spans 3.53 - 53.53 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 alcohol preference locus on Chr5 at D5Mit11 (47.40 Mbp , Build 37)
Description:
alcohol preference locus spans 22.40 - 72.40 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 alcohol preference locus on Chr5 at D5Mit11 (47.40 Mbp , Build 37)
Description:
alcohol preference locus spans 22.40 - 72.40 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 D5Rik85 (47.40 Mbp , Build 37)
Description:
METH responses for climbing spans 22.40 - 72.40 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 Acute ethanol sensitivity on Chr5 at NA (47.40 Mbp , Build 37)
Description:
Acute ethanol sensitivity spans 22.40 - 72.40 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).
Authors:
Radcliffe RA, Bohl ML, Lowe MV, Cycowski CS, Wehner JM
None - Basal gene expression profiles between C57BL/6J, DBA/2J, 129P3/J, and SWR/J strains DNA microarray Change in gene expression Two-way analysis of variance (ANOVA). 3,457 probe sets (corresponded to 2,870 different transcripts) with significant inter-strain differences (differ by at least 1.2-fold) - False discovery rate [FDR] < 1%, , rank > 3. Such a large disparity in the mouse striatal transcriptome was estimated by comparing nine array replicates prepared per strain from all of the treatment groups. More than half of the identified probe sets exhibited markedly significant results (1,735 with rank > 7). (NIF Method ID 84.1)
Authors:
Korostynski M, Piechota M, Kaminska D, Solecki W, Przewlocki R
Genes associated with Homo sapiens that interact with the MeSH term 'Vitamin K 3' (D024483). Incorporates data from 82 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 'Cyclosporine' (D016572). Incorporates data from 1 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 'Particulate Matter' (D052638). 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 'butyraldehyde' (C018475). Incorporates data from 7 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 'Selenium Compounds' (D018036). Incorporates data from 1386 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 'Sodium Selenite' (D018038). Incorporates data from 10 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 'Phenobarbital' (D010634). Incorporates data from 15 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 'Valproic Acid' (D014635). Incorporates data from 1238 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 'pirinixic acid' (C006253). Incorporates data from 1 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 'Quercetin' (D011794). Incorporates data from 6 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
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