Disease table of FEINGOLD SYNDROME OMIM ID: PS164280

Gene-disease associations table

GeneAssociated with FEINGOLD SYNDROME inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
MYCNClinVar, OMIM, HUMSAVARHGNC link2p24.31PS164280
MIR17HGOMIMHGNC link13q31.31PS164280

Download the disease annotation in CSV format

Relations among genes:

Tandem repeat annotations from DGD
Cytogenetic band analysis
Transcription Factors (TF) annotation from TRRUST
TFassociated to this disease# regulated genesRegulated genes# regulated genes associated with this diseaseRegulated genes associated with this disease
MYCNYES44MCM8, MCM7, HDAC2, TP53, BIRC5, IFNG, HLA-F, MCM3, LRRN3, BMI1, SKP2, MDM2, ABCB1, MCM2, DDB1, NES, CD44, HLA-C, HLA-G, CDKN1A, TP53INP1, HLA-B, NGFR, HLA-A, CIITA, MCM6, CTSD, ABCC1, LXN, DKK3, BAX, CDK6, HLA-E, NDRG1, TH, EFNB3, ID2, MCM5, MCM10, MYCL, TERT, NTRK1, MCM4, CDKN1B0
regulated geneassociated to this disease# TFsTFs # TFs associated with this diseaseTFs associated with this disease
MYCNYES15WT1, SP1, HOXA10, GATA3, HOXA9, HDAC2, ID2, YBX1, NCOR2, MXI1, ENO1, BIN1, SP3, E2F1, PAX50
Interactions from BIOGRID - physical
Interactions from BIOGRID - genetic
Interactions from STRING
Interactions from CORUM
Interactions from CENSUS
Interactions from PDB
Interactions from manually curated literature
KEGG pathways annotation: shared terms / NET-GE enrichment (no shared terms)
REACTOME pathways annotation: shared terms / NET-GE enrichment (no shared terms)
GO - molecular function annotation: shared terms / NET-GE enrichment (no shared terms)
GO - biological process annotation: shared terms / NET-GE enrichment (no shared terms)
GO - cellular component annotation: shared terms (no NET-GE enrichment)

Shared terms

GOICNumber of genes with the same GOGenes
membrane part (GO:0044425) 0.952MIR17HG, MYCN
integral component of membrane (GO:0016021) 1.142MIR17HG, MYCN
membrane (GO:0016020) 0.682MIR17HG, MYCN
intrinsic component of membrane (GO:0031224) 1.132MIR17HG, MYCN