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  2. Kidneyome_SuperPanel_KidGen_VCGS
  3. APOL1
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Kidneyome_SuperPanel_KidGen_VCGS

Gene: APOL1

Amber List (moderate evidence)
APOL1 (apolipoprotein L1)
EnsemblGeneIds (GRCh38): ENSG00000100342
EnsemblGeneIds (GRCh37): ENSG00000100342
OMIM: 603743, Gene2Phenotype
APOL1 is in 5 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Amber
Phenotypes
  • {Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551
OMIM
603743
Clinvar variants
Variants in APOL1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

24 Dec 2019, Gel status: 2

Set Phenotypes

Ivone Leong (Genomics England Curator)

Added phenotypes {Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551 for gene: APOL1

23 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: APOL1 was added gene: APOL1 was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: Expert Review Amber,Victorian Clinical Genetics Services Mode of inheritance for gene: APOL1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: APOL1 were set to 20635188; 20647424; 24206458 Phenotypes for gene: APOL1 were set to {Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551