Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic
Gene: TMEM260EnsemblGeneIds (GRCh38): ENSG00000070269
EnsemblGeneIds (GRCh37): ENSG00000070269
OMIM: 617449, Gene2Phenotype
TMEM260 is in 5 panels
1 review
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)
Seven unrelated families reported. Clinical features: ventricular septal defects (12/12), mostly secondary to truncus arteriosus (10/12), elevated creatinine levels (6/12), horse-shoe kidneys (1/12) and renal cysts (1/12) in patients.
Sources: Expert ReviewCreated: 3 Dec 2021, 8:49 p.m. | Last Modified: 3 Dec 2021, 8:53 p.m.
Panel Version: 0.98
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Structural heart defects and renal anomalies syndrome, MIM# 617478
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Expert Review
- Phenotypes
-
- Structural heart defects and renal anomalies syndrome, MIM# 617478
- OMIM
- 617449
- Clinvar variants
- Variants in TMEM260
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tmem260 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tmem260 has been classified as Green List (High Evidence).
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: TMEM260 were set to 28318500
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: tmem260 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)gene: TMEM260 was added gene: TMEM260 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic. Sources: Expert Review Mode of inheritance for gene: TMEM260 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TMEM260 were set to 28318500 Phenotypes for gene: TMEM260 were set to Structural heart defects and renal anomalies syndrome, MIM# 617478 Review for gene: TMEM260 was set to AMBER