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Mendeliome

Gene: GC

Red List (low evidence)

GC (GC, vitamin D binding protein)
EnsemblGeneIds (GRCh38): ENSG00000145321
EnsemblGeneIds (GRCh37): ENSG00000145321
OMIM: 139200, Gene2Phenotype
GC is in 1 panel

1 review

Natalie Tan (Victorian Clinical Genetics Services)

Red List (low evidence)

Currently no evidence for Mendelian gene disease association
Created: 19 Feb 2020, 11:01 p.m. | Last Modified: 19 Feb 2020, 11:01 p.m.
Panel Version: 0.1412

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
139200
Clinvar variants
Variants in GC
Penetrance
None
Panels with this gene

History Filter Activity

19 Feb 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

19 Feb 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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