Kidneyome_SuperPanel_KidGen_VCGS
Gene: UMODEnsemblGeneIds (GRCh38): ENSG00000169344
EnsemblGeneIds (GRCh37): ENSG00000169344
OMIM: 191845, Gene2Phenotype
UMOD is in 13 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- Victorian Clinical Genetics Services
- KidGen_Cystic v38.1.0
- KidGen_Tubulointerstitial v38.1.0
- OMIM
- 191845
- Clinvar variants
- Variants in UMOD
- Penetrance
- None
- Panels with this gene
-
- CAKUT
- Childhood onset dystonia, chorea or related movement disorder
- Unexplained kidney failure in young people
- Likely inborn error of metabolism
- Tubulointerstitial kidney disease
- Rare multisystem ciliopathy disorders
- Renal tubulopathies
- Undiagnosed metabolic disorders
- Cystic kidney disease
- Renal ciliopathies
- Skeletal dysplasia
- Thoracic dystrophies
- Primary ciliary disorders
History Filter Activity
Added New Source, Status Update
Ivone Leong (Genomics England Curator)Source Expert Review Green was added to UMOD. Rating Changed from Red List (low evidence) to Green List (high evidence)
Added New Source, Added New Source, Status Update
Ivone Leong (Genomics England Curator)Source Expert Review Red was added to UMOD. Source Victorian Clinical Genetics Services was added to UMOD. Rating Changed from Green List (high evidence) to Red List (low evidence)
Added New Source
Ivone Leong (Genomics England Curator)Source KidGen_Cystic v38.1.0 was added to UMOD.
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: UMOD was added gene: UMOD was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: KidGen_Tubulointerstitial v38.1.0,Expert Review Green Mode of inheritance for gene: UMOD was set to Unknown