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  2. GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH
  3. DCAF10
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GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH

Gene: DCAF10

Red List (low evidence)
DCAF10 (DDB1 and CUL4 associated factor 10)
EnsemblGeneIds (GRCh38): ENSG00000122741
EnsemblGeneIds (GRCh37): ENSG00000122741
DCAF10 is in 3 panels

1 review

Emily Jones (North Bristol NHS Trust)

Red List (low evidence)

Not on OMIM. Unable to find any reference to disease assciation of literature search.
Created: 9 Jul 2019, 3:59 p.m. | Last Modified: 9 Jul 2019, 3:59 p.m.
Panel Version: 0.10
Created: 9 Jul 2019, 3:59 p.m.
Last Modified: 9 Jul 2019, 3:59 p.m.
Panel version: 0.10

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • South West GLH
Clinvar variants
Variants in DCAF10
Penetrance
None
Panels with this gene

History Filter Activity

9 Jul 2019, Gel status: 1

Set mode of inheritance

Louise Daugherty (Genomics England Curator)

Mode of inheritance for gene DCAF10 was changed from to BIALLELIC, autosomal or pseudoautosomal

2 Apr 2019, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

Source Expert Review Red was added to DCAF10.

2 Apr 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: DCAF10 was added gene: DCAF10 was added to GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH. Sources: South West GLH Mode of inheritance for gene: DCAF10 was set to