Information on TRIM22

Basic details

Alt. symbols: STAF50 | GPSTAF50 | RNF94

Approved name: tripartite motif containing 22
Alt. names: tripartite motif-containing 22

Location: 11p15.4: 5689610 - 5737089 (+)
Gene type: protein_coding, 18 transcripts.

Scores: LoFtool: 0.586000 | pLI: 0.00000000 | LOEUF: 0.990

HGNC: 16379

NCBI: 10346, RefSeq: .0

Ensembl: ENSG00000132274.17

LRG_ | Status: none

OMIM: 606559

Expression | ProteinAtlas

Normal function

Dysfunction and disease

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[Gene NOT reviewed yet]

Associated conditions

Acronym Condition's_name MOI Mode_of_actionwww icon OMIM_ID No.cases
IBD32 Inflammatory bowel disease 32 ARdict. icon - 0 (0 fams)

Please mind that full curation (inclusion of all published patients) of this gene has not started yet. Please contact us if you want to volunteer.

Transcripts of TRIM22

Name ENSEMBL_ID LRG_ID CCDS_ID MANE Transcript.type Exons Canonical CDS_length REFSEQ_ID
201 ENST00000379965.8 CCDS41612 Select protein_coding 8 Yes 2888 NM_001199573,NM_006074

Published variants

Found 0 variants

Var.name Exon/Intron cDNA_pos. CDS_change Prot.change Var.type Var.class. Patients

Please mind that full curation (inclusion of all published variants) of this gene has not started yet. Please contact us if you want to volunteer.

Diagnostic pitfalls & paradigms

Considerations to take into account when analyzing this gene

Year Paradigm ⓘ PMID Notes
- Regions of Homology -
-Cryptic splicing-Unreported or not recorded in our DB.
-Uniparental disomy-Unreported or not recorded in our DB.
-Mosaicism-Unreported or not recorded in our DB.
-Incomplete penetrance-Unreported or not recorded in our DB.
-Di-/oligo-genic inheritance-Unreported or not recorded in our DB.
-Somatic reversion-Unreported or not recorded in our DB.

References linked to variants in TRIM22

ID Year Title Journal PMID Variants

Phenotypic & functional assays available?

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