1. Panels
  2. Proteinuria
  3. MYO1E
STRs in panel
Prev Next
Regions in panel
Prev Next

Proteinuria

Gene: MYO1E

Green List (high evidence)
MYO1E (myosin IE)
EnsemblGeneIds (GRCh38): ENSG00000157483
EnsemblGeneIds (GRCh37): ENSG00000157483
OMIM: 601479, Gene2Phenotype
MYO1E is in 4 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

At least 3 unrelated families and functional data.
Created: 14 May 2022, 3:17 a.m. | Last Modified: 14 May 2022, 3:17 a.m.
Panel Version: 0.197

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Glomerulosclerosis, focal segmental, 6, MIM# 614131

Publications

Created: 14 May 2022, 3:17 a.m.
Last Modified: 14 May 2022, 3:17 a.m.
Panel version: 0.197

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Glomerulosclerosis, focal segmental, 6, MIM# 614131
OMIM
601479
Clinvar variants
Variants in MYO1E
Penetrance
None
Publications
Panels with this gene

History Filter Activity

14 May 2022, Gel status: 3

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: myo1e has been classified as Green List (High Evidence).

14 May 2022, Gel status: 3

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: MYO1E were changed from to Glomerulosclerosis, focal segmental, 6, MIM# 614131

14 May 2022, Gel status: 3

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: MYO1E were set to

14 May 2022, Gel status: 3

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: MYO1E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: MYO1E was added gene: MYO1E was added to Nephrotic Syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: MYO1E was set to Unknown