Leukodystrophy Victorian Clinical Genetics Services
Gene: COL4A1EnsemblGeneIds (GRCh38): ENSG00000187498
EnsemblGeneIds (GRCh37): ENSG00000187498
OMIM: 120130, Gene2Phenotype
COL4A1 is in 25 panels
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Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 120130
- Clinvar variants
- Variants in COL4A1
- Penetrance
- None
- Panels with this gene
-
- Adult onset neurodegenerative disorder
- DDG2P
- Proteinuric renal disease
- Thoracic aortic aneurysm or dissection
- Haematuria
- Bilateral congenital or childhood onset cataracts
- Familial cerebral small vessel disease
- White matter disorders and cerebral calcification - narrow panel
- Glaucoma (developmental)
- Arthrogryposis
- Malformations of cortical development
- Congenital muscular dystrophy
- Structural eye disease
- Early onset or syndromic epilepsy
- Fetal anomalies
- Retinal disorders
- Anophthalmia or microphthalmia
- Thoracic aortic aneurysm or dissection (GMS)
- Intracerebral calcification disorders
- Cystic kidney disease
- Inherited white matter disorders
- Cerebral vascular malformations
- Adult onset leukodystrophy
- Intellectual disability
- Hydrocephalus
History Filter Activity
Added New Source
Sarah Leigh (Genomics England Curator)COL4A1 was added to Leukodystrophy Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
Created
Sarah Leigh (Genomics England Curator)COL4A1 was created by Sarah Leigh