Hypertrophic cardiomyopathy_HCM
Gene: TULP3EnsemblGeneIds (GRCh38): ENSG00000078246
EnsemblGeneIds (GRCh37): ENSG00000078246
OMIM: 604730, Gene2Phenotype
TULP3 is in 5 panels
3 reviews
Bryony Thompson (Royal Melbourne Hospital)
Comment on list classification: Currently, only 3 adult individuals from 2 unrelated families presented with hypertrophic non-obstructive cardiomyopathy (HNCM). More evidence required for the HCM associationCreated: 22 Aug 2024, 8:24 a.m. | Last Modified: 22 Aug 2024, 8:24 a.m.
Panel Version: 0.182
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hepatorenocardiac degenerative fibrosis, MIM# 619902
Anna Ritchie (Victorian Clinical Genetics Services)
15 individuals from eight unrelated families with bi-allelic variants in TULP3 were detected. The affected individuals reported are mostly adults, in the 3rd through 7th decades of life, and presented with progressive degenerative liver fibrosis with variable fibrocystic kidney disease and hypertrophic cardiomyopathy.
The human phenotype was ecapitulated in adult zebrafish and confirmed disruption of critical ciliary cargo composition in several primary cell lines derived from affected individuals
Sources: LiteratureCreated: 5 May 2022, 1:50 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
progressive degenerative liver fibrosis with variable fibrocystic kidney disease; hypertrophic cardiomyopathy MONDO:0005045
Publications
- PMID: 35397207
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Phenotypes
-
- Hepatorenocardiac degenerative fibrosis, MIM# 619902
- OMIM
- 604730
- Clinvar variants
- Variants in TULP3
- Penetrance
- None
- Publications
-
- PMID: 35397207
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: tulp3 has been classified as Amber List (Moderate Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: TULP3 were changed from progressive degenerative liver fibrosis with variable fibrocystic kidney disease; hypertrophic cardiomyopathy MONDO:0005045 to Hepatorenocardiac degenerative fibrosis, MIM# 619902
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: tulp3 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: tulp3 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: tulp3 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Alison Yeung (Victorian Clinical Genetics Services)Gene: tulp3 has been removed from the panel.
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Anna Ritchie (Victorian Clinical Genetics Services)gene: TULP3 was added gene: TULP3 was added to Hypertrophic cardiomyopathy_HCM. Sources: Literature Mode of inheritance for gene: TULP3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TULP3 were set to PMID: 35397207 Phenotypes for gene: TULP3 were set to progressive degenerative liver fibrosis with variable fibrocystic kidney disease; hypertrophic cardiomyopathy MONDO:0005045