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Mendeliome

Gene: GLRX3

Red List (low evidence)

GLRX3 (glutaredoxin 3)
EnsemblGeneIds (GRCh38): ENSG00000108010
EnsemblGeneIds (GRCh37): ENSG00000108010
OMIM: 612754, Gene2Phenotype
GLRX3 is in 1 panel

1 review

Bryony Thompson (Royal Melbourne Hospital)

Red List (low evidence)

Cannot find any evidence that this gene is associated with Mendelian disease. A null zebrafish model lacked visible red blood cells in the heart, impacting heme synthesis and reduced the amount and activity of iron-dependent enzymes.
Created: 4 Feb 2021, 11:27 p.m. | Last Modified: 4 Feb 2021, 11:27 p.m.
Panel Version: 0.6216

Mode of inheritance
Unknown

Publications

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
612754
Clinvar variants
Variants in GLRX3
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: glrx3 has been classified as Red List (Low Evidence).

20 May 2022, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: GLRX3 were set to

4 Feb 2021, Gel status: 1

Entity classified by Genomics England curator

Bryony Thompson (Royal Melbourne Hospital)

Gene: glrx3 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: GLRX3 was added gene: GLRX3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: GLRX3 was set to Unknown