This Panel is marked as Deleted
Kidneyome_SuperPanel_KidGen_VCGS
Gene: ATXN10
ATXN10 (ataxin 10)
EnsemblGeneIds (GRCh38): ENSG00000130638
EnsemblGeneIds (GRCh37): ENSG00000130638
OMIM: 611150, Gene2Phenotype
ATXN10 is in 17 panels
EnsemblGeneIds (GRCh38): ENSG00000130638
EnsemblGeneIds (GRCh37): ENSG00000130638
OMIM: 611150, Gene2Phenotype
ATXN10 is in 17 panels
0 reviews
Details
- Mode of Inheritance
- Unknown
- Sources
-
- Expert Review Green
- KidGen_CilioNephronop v38.1.0
- OMIM
- 611150
- Clinvar variants
- Variants in ATXN10
- Penetrance
- None
- Panels with this gene
-
- Hereditary neuropathy or pain disorder
- Hereditary ataxia
- Ataxia and cerebellar anomalies - narrow panel
- Hereditary ataxia with onset in adulthood
- Intellectual disability
- Early onset dementia (encompassing fronto-temporal dementia and prion disease)
- Childhood onset hereditary spastic paraplegia
- Adult onset neurodegenerative disorder
- Childhood onset dystonia, chorea or related movement disorder
- Early onset dystonia
- Hereditary spastic paraplegia
- Rare multisystem ciliopathy disorders
- Adult onset hereditary spastic paraplegia
- Skeletal dysplasia
- Hereditary neuropathy
- Thoracic dystrophies
- Primary ciliary disorders
History Filter Activity
23 Dec 2019, Gel status: 3
Created, Added New Source, Set mode of inheritance
Ivone Leong (Genomics England Curator)gene: ATXN10 was added gene: ATXN10 was added to Kidneyome_SuperPanel_KidGen_VCGS. Sources: KidGen_CilioNephronop v38.1.0,Expert Review Green Mode of inheritance for gene: ATXN10 was set to Unknown