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Mendeliome

Gene: APOC4-APOC2

Red List (low evidence)

APOC4-APOC2 (APOC4-APOC2 readthrough (NMD candidate))
EnsemblGeneIds (GRCh38): ENSG00000224916
EnsemblGeneIds (GRCh37): ENSG00000224916
APOC4-APOC2 is in 1 panel

1 review

Elena Savva (Victorian Clinical Genetics Services)

Red List (low evidence)

No association to Mendelian disease

PMID: 31034468 - single paper reported this readthrough event, describes a GWAS study associating the locus low-density lipoprotein (LDL)
Created: 6 May 2022, 5:01 a.m. | Last Modified: 6 May 2022, 5:01 a.m.
Panel Version: 0.13871

Publications

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Clinvar variants
Variants in APOC4-APOC2
Penetrance
None
Publications
Panels with this gene

History Filter Activity

6 May 2022, Gel status: 1

Entity classified by Genomics England curator

Elena Savva (Victorian Clinical Genetics Services)

Gene: apoc4-apoc2 has been classified as Red List (Low Evidence).

6 May 2022, Gel status: 1

Set publications

Elena Savva (Victorian Clinical Genetics Services)

Publications for gene: APOC4-APOC2 were set to

6 May 2022, Gel status: 1

Entity classified by Genomics England curator

Elena Savva (Victorian Clinical Genetics Services)

Gene: apoc4-apoc2 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: APOC4-APOC2 was added gene: APOC4-APOC2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: APOC4-APOC2 was set to Unknown