This Panel is marked as Deleted
Metabolic renal disease_KidGen
Gene: RMND1
RMND1 (required for meiotic nuclear division 1 homolog)
EnsemblGeneIds (GRCh38): ENSG00000155906
EnsemblGeneIds (GRCh37): ENSG00000155906
OMIM: 614917, Gene2Phenotype
RMND1 is in 11 panels
EnsemblGeneIds (GRCh38): ENSG00000155906
EnsemblGeneIds (GRCh37): ENSG00000155906
OMIM: 614917, Gene2Phenotype
RMND1 is in 11 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- KidGen_MetabolicRenal v38.1.0
- OMIM
- 614917
- Clinvar variants
- Variants in RMND1
- Penetrance
- None
- Panels with this gene
-
- Likely inborn error of metabolism
- Intellectual disability
- Possible mitochondrial disorder - nuclear genes
- Early onset or syndromic epilepsy
- Renal tubulopathies
- Unexplained young onset end-stage renal disease - additional genes
- Undiagnosed metabolic disorders
- Fetal anomalies
- DDG2P
- Childhood onset dystonia, chorea or related movement disorder
- Mitochondrial disorders
History Filter Activity
23 Dec 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: RMND1 was added gene: RMND1 was added to Metabolic renal disease_KidGen. Sources: KidGen_MetabolicRenal v38.1.0,Expert Review Green Mode of inheritance for gene: RMND1 was set to Unknown