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Mendeliome

Gene: ORMDL3

Red List (low evidence)

ORMDL3 (ORMDL sphingolipid biosynthesis regulator 3)
EnsemblGeneIds (GRCh38): ENSG00000172057
EnsemblGeneIds (GRCh37): ENSG00000172057
OMIM: 610075, Gene2Phenotype
ORMDL3 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Associated with susceptibility to asthma, cannot find link to Mendelian disease.
Created: 20 Jul 2020, 4:50 a.m. | Last Modified: 20 Jul 2020, 4:50 a.m.
Panel Version: 0.3412

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
610075
Clinvar variants
Variants in ORMDL3
Penetrance
None
Panels with this gene

History Filter Activity

20 Jul 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ormdl3 has been classified as Red List (Low Evidence).

20 Jul 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ormdl3 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: ORMDL3 was added gene: ORMDL3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ORMDL3 was set to Unknown