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  2. Infantile enterocolitis & monogenic inflammatory bowel disease
  3. TRIM22
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Infantile enterocolitis & monogenic inflammatory bowel disease

Gene: TRIM22

No list
TRIM22 (tripartite motif containing 22)
EnsemblGeneIds (GRCh38): ENSG00000132274
EnsemblGeneIds (GRCh37): ENSG00000132274
OMIM: 606559, Gene2Phenotype
TRIM22 is in 3 panels

1 review

Zornitza Stark (Australian Genomics)

Green List (high evidence)

Three unrelated families reported with bi-allelic variants in this gene, and very early onset IBD, some functional data.
Sources: Expert list
Created: 25 Aug 2020, 8:37 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Inflammatory bowel disease

Publications

Variants in this GENE are reported as part of current diagnostic practice

Created: 25 Aug 2020, 8:37 a.m.

Panel version: 1.16

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
Phenotypes
  • Inflammatory bowel disease
OMIM
606559
Clinvar variants
Variants in TRIM22
Penetrance
None
Publications
Panels with this gene

History Filter Activity

25 Aug 2020, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Zornitza Stark (Australian Genomics)

gene: TRIM22 was added gene: TRIM22 was added to Infantile enterocolitis & monogenic inflammatory bowel disease. Sources: Expert list Mode of inheritance for gene: TRIM22 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TRIM22 were set to 26836588 Phenotypes for gene: TRIM22 were set to Inflammatory bowel disease Review for gene: TRIM22 was set to GREEN gene: TRIM22 was marked as current diagnostic