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  2. BRIDGE_SPEED_NEURO_v2.0_20160416
  3. SLC2A10
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BRIDGE_SPEED_NEURO_v2.0_20160416

Gene: SLC2A10

Red List (low evidence)
SLC2A10 (solute carrier family 2 member 10)
EnsemblGeneIds (GRCh38): ENSG00000197496
EnsemblGeneIds (GRCh37): ENSG00000197496
OMIM: 606145, Gene2Phenotype
SLC2A10 is in 7 panels

1 review

BRIDGE consortium (NIHRBR-RD)

Green List (high evidence)

ddg2p_20141118; ddg2p_20141118_conf; ddg2p_201507; ddg2p_201507_conf; neuro_20160418_strict; Loss of function
Created: 7 Feb 2017, 4:54 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Arterial tortuosity syndrome, 208050

Variants in this GENE are reported as part of current diagnostic practice

Created: 7 Feb 2017, 4:54 p.m.

Panel version: 0.2

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • BRIDGE
Phenotypes
  • Arterial tortuosity syndrome, 208050
OMIM
606145
Clinvar variants
Variants in SLC2A10
Penetrance
Complete
Panels with this gene

History Filter Activity

7 Feb 2017, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

SLC2A10 was created by ellenmcdonagh

7 Feb 2017, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

SLC2A10 was added to BRIDGE_SPEED_NEURO_v2.0_20160416panel. Sources: BRIDGE