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Mendeliome

Gene: DECR1

Red List (low evidence)

DECR1 (2,4-dienoyl-CoA reductase 1)
EnsemblGeneIds (GRCh38): ENSG00000104325
EnsemblGeneIds (GRCh37): ENSG00000104325
OMIM: 222745, Gene2Phenotype
DECR1 is in 3 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence for Mendelian disease association.
Created: 6 May 2022, 8:21 a.m. | Last Modified: 6 May 2022, 8:21 a.m.
Panel Version: 0.13907

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
222745
Clinvar variants
Variants in DECR1
Penetrance
None
Panels with this gene

History Filter Activity

6 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: decr1 has been classified as Red List (Low Evidence).

6 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: decr1 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: DECR1 was added gene: DECR1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: DECR1 was set to Unknown