Structural eye disease
Gene: ALMS1
ALMS1 (ALMS1, centrosome and basal body associated protein)
EnsemblGeneIds (GRCh38): ENSG00000116127
EnsemblGeneIds (GRCh37): ENSG00000116127
OMIM: 606844, Gene2Phenotype
ALMS1 is in 24 panels
EnsemblGeneIds (GRCh38): ENSG00000116127
EnsemblGeneIds (GRCh37): ENSG00000116127
OMIM: 606844, Gene2Phenotype
ALMS1 is in 24 panels
2 reviews
Nicola Ragge (Birmingham Women's and Children's NHS Foundation Hospital Trust)
retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 19 Jun 2019, 3:32 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Alstrom syndrome; 203800
Ivone Leong (Genomics England Curator)
Submitted on behalf of Professor Nicola Ragge (Wessex and West Midlands GLH). retinal gene, can't find any evidence that it is associated with structural eye diseaseCreated: 17 Apr 2019, 3:30 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Alstrom syndrome 203800
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- NHS GMS
- Expert Review Red
- Phenotypes
-
- Alstrom syndrome 203800
- Eye Disorders
- OMIM
- 606844
- Clinvar variants
- Variants in ALMS1
- Penetrance
- None
- Panels with this gene
-
- Paediatric or syndromic cardiomyopathy
- Ophthalmological ciliopathies
- Insulin resistance (including lipodystrophy)
- Intellectual disability
- Dilated Cardiomyopathy and conduction defects
- Alstrom syndrome
- Monogenic diabetes
- Structural eye disease
- Diabetes with additional phenotypes suggestive of a monogenic aetiology
- Renal ciliopathies
- Monogenic hearing loss
- Fetal anomalies
- Severe early-onset obesity
- Childhood onset dystonia, chorea or related movement disorder
- Bardet Biedl syndrome
- Unexplained kidney failure in young people
- Ductal plate malformation
- Proteinuric renal disease
- Lipodystrophy - childhood onset
- Limb disorders
- DDG2P
- Retinal disorders
- Glaucoma (developmental)
- Rare multisystem ciliopathy disorders
History Filter Activity
17 Apr 2019, Gel status: 1
Added New Source, Set mode of inheritance, Set Phenotypes
Ivone Leong (Genomics England Curator)Source NHS GMS was added to ALMS1. Mode of inheritance for gene ALMS1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Alstrom syndrome 203800 for gene: ALMS1
3 Jan 2019, Gel status: 1
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ellen McDonagh (Genomics England Curator)gene: ALMS1 was added gene: ALMS1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ALMS1 was set to Phenotypes for gene: ALMS1 were set to Eye Disorders