Disease table of SMITH-MCCORT DYSPLASIA OMIM ID: PS607326
Gene-disease associations table
Gene | Associated with SMITH-MCCORT DYSPLASIA in | Link to HGNC | Cytogenetic band | Number of associated diseases | Associated diseases |
DYM | ClinVar, OMIM, HUMSAVAR | HGNC link | 18q21.1 | 2 | 223800, PS607326 |
RAB33B | ClinVar, OMIM, HUMSAVAR | HGNC link | 4q31.1 | 1 | PS607326 |
Download the disease annotation in CSV format
Relations among genes:
Tandem repeat annotations from DGD
Cytogenetic band analysis
Transcription Factors (TF) annotation from TRRUST
Interactions from BIOGRID - physical
Interactions from BIOGRID - genetic
Interactions from STRING
Gene1 | Gene2 | Direct Interaction | Interaction mode | Number of shared interactors | Shared genes in interaction |
DYM | RAB33B | Yes | binding, expression | 0 | |
Direct interactions graph
Interactions graph (direct and indirect interactions, when direct are not available)
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 (no NET-GE enrichment)
Shared terms
GO - biological process annotation: shared terms (no NET-GE enrichment)
Shared terms
GO - cellular component annotation: shared terms / NET-GE enrichment
Shared terms
NET-GE enrichment