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Intellectual disability syndromic and non-syndromic

Gene: TRIM37

Red List (low evidence)

TRIM37 (tripartite motif containing 37)
EnsemblGeneIds (GRCh38): ENSG00000108395
EnsemblGeneIds (GRCh37): ENSG00000108395
OMIM: 605073, Gene2Phenotype
TRIM37 is in 13 panels

1 review

Chirag Patel (Genetic Health Queensland)

Red List (low evidence)

No ID in this condition.
Created: 5 Dec 2019, 11:59 a.m. | Last Modified: 5 Dec 2019, 11:59 a.m.
Panel Version: 0.528

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Mulibrey nanism; OMIM #253250

History Filter Activity

11 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: trim37 has been classified as Red List (Low Evidence).

5 Dec 2019, Gel status: 1

Entity classified by Genomics England curator

Chirag Patel (Genetic Health Queensland)

Gene: trim37 has been classified as Red List (Low Evidence).

5 Dec 2019, Gel status: 3

Removed Source, Added New Source, Set mode of inheritance, Set Phenotypes

Chirag Patel (Genetic Health Queensland)

Source Genetic Health Queensland was removed from TRIM37. Source Expert list was added to TRIM37. Mode of inheritance for gene TRIM37 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TRIM37 were changed from to Mulibrey nanism; OMIM #253250

22 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: TRIM37 was added gene: TRIM37 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland Mode of inheritance for gene: TRIM37 was set to Unknown