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  3. ARHGAP24
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Proteinuria

Gene: ARHGAP24

Red List (low evidence)
ARHGAP24 (Rho GTPase activating protein 24)
EnsemblGeneIds (GRCh38): ENSG00000138639
EnsemblGeneIds (GRCh37): ENSG00000138639
OMIM: 610586, Gene2Phenotype
ARHGAP24 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

One family reported initially; variant is present in >100 individuals in gnomad, and also in one individual in homozygous state.
Created: 9 Jan 2020, 3:26 a.m. | Last Modified: 9 Jan 2020, 3:26 a.m.
Panel Version: 0.69

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
FSGS, MONDO:0005363, ARHGAP24-related

Publications

Created: 9 Jan 2020, 3:26 a.m.
Last Modified: 9 Jan 2020, 3:26 a.m.
Panel version: 0.220

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • FSGS, MONDO:0005363, ARHGAP24-related
OMIM
610586
Clinvar variants
Variants in ARHGAP24
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Sep 2023, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: ARHGAP24 were changed from FSGS to FSGS, MONDO:0005363, ARHGAP24-related

9 Jan 2020, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: ARHGAP24 were set to 21911940

9 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: arhgap24 has been classified as Red List (Low Evidence).

9 Jan 2020, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: ARHGAP24 were changed from to FSGS

9 Jan 2020, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: ARHGAP24 were set to

9 Jan 2020, Gel status: 1

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: ARHGAP24 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

9 Jan 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: arhgap24 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ARHGAP24 was added gene: ARHGAP24 was added to Nephrotic Syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ARHGAP24 was set to Unknown