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Generate a map
About
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Generate a map
About
Set the parameters for a new submission
Disease identifier:
Orphanet id:
HPO ids:
OR
MINERVA map ids:
ramap.elixir-luxembourg.org
asthma.uni.lu
covid19map.elixir-luxembourg.org
progeria.uni.lu
pathwaylab.elixir-luxembourg.org
pdmap.uni.lu
Enrichr db pathways:
Genome_Browser_PWMs
TRANSFAC_and_JASPAR_PWMs
Transcription_Factor_PPIs
ChEA_2013
Drug_Perturbations_from_GEO_2014
ENCODE_TF_ChIP-seq_2014
BioCarta_2013
Reactome_2013
WikiPathways_2013
Disease_Signatures_from_GEO_up_2014
KEGG_2013
TF-LOF_Expression_from_GEO
TargetScan_microRNA
PPI_Hub_Proteins
GO_Molecular_Function_2015
GeneSigDB
Chromosome_Location
Human_Gene_Atlas
Mouse_Gene_Atlas
GO_Cellular_Component_2015
GO_Biological_Process_2015
Human_Phenotype_Ontology
Epigenomics_Roadmap_HM_ChIP-seq
KEA_2013
NURSA_Human_Endogenous_Complexome
CORUM
SILAC_Phosphoproteomics
MGI_Mammalian_Phenotype_Level_3
MGI_Mammalian_Phenotype_Level_4
Old_CMAP_up
Old_CMAP_down
OMIM_Disease
OMIM_Expanded
VirusMINT
MSigDB_Computational
MSigDB_Oncogenic_Signatures
Disease_Signatures_from_GEO_down_2014
Virus_Perturbations_from_GEO_up
Virus_Perturbations_from_GEO_down
Cancer_Cell_Line_Encyclopedia
NCI-60_Cancer_Cell_Lines
Tissue_Protein_Expression_from_ProteomicsDB
Tissue_Protein_Expression_from_Human_Proteome_Map
HMDB_Metabolites
Pfam_InterPro_Domains
GO_Biological_Process_2013
GO_Cellular_Component_2013
GO_Molecular_Function_2013
Allen_Brain_Atlas_up
ENCODE_TF_ChIP-seq_2015
ENCODE_Histone_Modifications_2015
Phosphatase_Substrates_from_DEPOD
Allen_Brain_Atlas_down
ENCODE_Histone_Modifications_2013
Achilles_fitness_increase
Achilles_fitness_decrease
MGI_Mammalian_Phenotype_2013
BioCarta_2015
HumanCyc_2015
KEGG_2015
NCI-Nature_2015
Panther_2015
WikiPathways_2015
Reactome_2015
ESCAPE
HomoloGene
Disease_Perturbations_from_GEO_down
Disease_Perturbations_from_GEO_up
Drug_Perturbations_from_GEO_down
Genes_Associated_with_NIH_Grants
Drug_Perturbations_from_GEO_up
KEA_2015
Gene_Perturbations_from_GEO_up
Gene_Perturbations_from_GEO_down
ChEA_2015
dbGaP
LINCS_L1000_Chem_Pert_up
LINCS_L1000_Chem_Pert_down
GTEx_Tissue_Expression_Down
GTEx_Tissue_Expression_Up
Ligand_Perturbations_from_GEO_down
Aging_Perturbations_from_GEO_down
Aging_Perturbations_from_GEO_up
Ligand_Perturbations_from_GEO_up
MCF7_Perturbations_from_GEO_down
MCF7_Perturbations_from_GEO_up
Microbe_Perturbations_from_GEO_down
Microbe_Perturbations_from_GEO_up
LINCS_L1000_Ligand_Perturbations_down
LINCS_L1000_Ligand_Perturbations_up
L1000_Kinase_and_GPCR_Perturbations_down
L1000_Kinase_and_GPCR_Perturbations_up
Reactome_2016
KEGG_2016
WikiPathways_2016
ENCODE_and_ChEA_Consensus_TFs_from_ChIP-X
Kinase_Perturbations_from_GEO_down
Kinase_Perturbations_from_GEO_up
BioCarta_2016
HumanCyc_2016
NCI-Nature_2016
Panther_2016
DrugMatrix
ChEA_2016
huMAP
Jensen_TISSUES
RNA-Seq_Disease_Gene_and_Drug_Signatures_from_GEO
MGI_Mammalian_Phenotype_2017
Jensen_COMPARTMENTS
Jensen_DISEASES
BioPlex_2017
GO_Cellular_Component_2017
GO_Molecular_Function_2017
GO_Biological_Process_2017
GO_Cellular_Component_2017b
GO_Molecular_Function_2017b
GO_Biological_Process_2017b
ARCHS4_Tissues
ARCHS4_Cell-lines
ARCHS4_IDG_Coexp
ARCHS4_Kinases_Coexp
ARCHS4_TFs_Coexp
SysMyo_Muscle_Gene_Sets
miRTarBase_2017
TargetScan_microRNA_2017
Enrichr_Libraries_Most_Popular_Genes
Enrichr_Submissions_TF-Gene_Coocurrence
Data_Acquisition_Method_Most_Popular_Genes
DSigDB
GO_Biological_Process_2018
GO_Cellular_Component_2018
GO_Molecular_Function_2018
TF_Perturbations_Followed_by_Expression
Chromosome_Location_hg19
NIH_Funded_PIs_2017_Human_GeneRIF
NIH_Funded_PIs_2017_Human_AutoRIF
Rare_Diseases_AutoRIF_ARCHS4_Predictions
Rare_Diseases_GeneRIF_ARCHS4_Predictions
NIH_Funded_PIs_2017_AutoRIF_ARCHS4_Predictions
NIH_Funded_PIs_2017_GeneRIF_ARCHS4_Predictions
Rare_Diseases_GeneRIF_Gene_Lists
Rare_Diseases_AutoRIF_Gene_Lists
SubCell_BarCode
GWAS_Catalog_2019
WikiPathways_2019_Human
WikiPathways_2019_Mouse
TRRUST_Transcription_Factors_2019
KEGG_2019_Human
KEGG_2019_Mouse
InterPro_Domains_2019
Pfam_Domains_2019
DepMap_WG_CRISPR_Screens_Broad_CellLines_2019
DepMap_WG_CRISPR_Screens_Sanger_CellLines_2019
MGI_Mammalian_Phenotype_Level_4_2019
UK_Biobank_GWAS_v1
BioPlanet_2019
ClinVar_2019
PheWeb_2019
DisGeNET
HMS_LINCS_KinomeScan
CCLE_Proteomics_2020
ProteomicsDB_2020
lncHUB_lncRNA_Co-Expression
Virus-Host_PPI_P-HIPSTer_2020
Elsevier_Pathway_Collection
Table_Mining_of_CRISPR_Studies
COVID-19_Related_Gene_Sets
MSigDB_Hallmark_2020
Enrichr_Users_Contributed_Lists_2020
TG_GATES_2020
Allen_Brain_Atlas_10x_scRNA_2021
Descartes_Cell_Types_and_Tissue_2021
KEGG_2021_Human
WikiPathway_2021_Human
HuBMAP_ASCT_plus_B_augmented_w_RNAseq_Coexpression
GO_Biological_Process_2021
GO_Cellular_Component_2021
GO_Molecular_Function_2021
MGI_Mammalian_Phenotype_Level_4_2021
CellMarker_Augmented_2021
Orphanet_Augmented_2021
COVID-19_Related_Gene_Sets_2021
PanglaoDB_Augmented_2021
Azimuth_Cell_Types_2021
PhenGenI_Association_2021
RNAseq_Automatic_GEO_Signatures_Human_Down
RNAseq_Automatic_GEO_Signatures_Human_Up
RNAseq_Automatic_GEO_Signatures_Mouse_Down
RNAseq_Automatic_GEO_Signatures_Mouse_Up
GTEx_Aging_Signatures_2021
HDSigDB_Human_2021
HDSigDB_Mouse_2021
HuBMAP_ASCTplusB_augmented_2022
FANTOM6_lncRNA_KD_DEGs
MAGMA_Drugs_and_Diseases
PFOCR_Pathways
Tabula_Sapiens
ChEA_2022
Diabetes_Perturbations_GEO_2022
LINCS_L1000_Chem_Pert_Consensus_Sigs
LINCS_L1000_CRISPR_KO_Consensus_Sigs
Tabula_Muris
Reactome_2022
SynGO_2022
GlyGen_Glycosylated_Proteins_2022
IDG_Drug_Targets_2022
KOMP2_Mouse_Phenotypes_2022
Metabolomics_Workbench_Metabolites_2022
Proteomics_Drug_Atlas_2023
Serine_Threonine_Kinome_Atlas_2023
Disgenet max genes:
Opentarget max genes:
Max network neighbors:
E-mail of the submitter:
Submit and start the job
How to use this form?
Please select the input parameters
Click the blue button to submit the new job, and request the computing
The processing will be queued once the request reaches the servers and you will be redirected towards your query page.
Once your query is treated, the results will be available in the query page
If you'd like to restart the job, or try out different parameters, you can do it from "Submissions" tab.