1. Panels
  2. Incidentalome_PREGEN_DRAFT
  3. TRIM33
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Incidentalome_PREGEN_DRAFT

Gene: TRIM33

Red List (low evidence)
TRIM33 (tripartite motif containing 33)
EnsemblGeneIds (GRCh38): ENSG00000197323
EnsemblGeneIds (GRCh37): ENSG00000197323
OMIM: 605769, Gene2Phenotype
TRIM33 is in 2 panels

1 review

Tony Roscioli (New South Wales Health Pathology)

Red List (low evidence)

Comment on list classification: Not a clear cause of a Mendelian disorder and so should be removed from the incidentalome gene panel
Created: 7 Jan 2021, 1:17 a.m. | Last Modified: 7 Jan 2021, 1:17 a.m.
Panel Version: 0.11
Not a clear cause of a Mendelian disorder - should be removed from the incidentalome panel
Created: 7 Jan 2021, 1:16 a.m. | Last Modified: 7 Jan 2021, 1:16 a.m.
Panel Version: 0.10
Created: 7 Jan 2021, 1:16 a.m.
Last Modified: 7 Jan 2021, 1:16 a.m.
Panel version: 0.10

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • NSW Health Pathology
OMIM
605769
Clinvar variants
Variants in TRIM33
Penetrance
None
Panels with this gene

History Filter Activity

7 Jan 2021, Gel status: 1

Entity classified by Genomics England curator

Tony Roscioli (New South Wales Health Pathology)

Gene: trim33 has been classified as Red List (Low Evidence).

9 Nov 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: TRIM33 was added gene: TRIM33 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: TRIM33 was set to Unknown