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Multiple Tumours

Gene: VSIG10L

Amber List (moderate evidence)
VSIG10L (V-set and immunoglobulin domain containing 10 like)
EnsemblGeneIds (GRCh38): ENSG00000186806
EnsemblGeneIds (GRCh37): ENSG00000186806
VSIG10L is in 0 panels

1 review

Sarah Leigh (Genomics England Curator)

Red List (low evidence)

Germline variant (p.S631G) segregating in affected members of large family (3 members with esophageal adenocarcinoma and 11 with Barrett esophagus). Supporting transfection and histological studies reported
Created: 9 May 2017, 7:54 a.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Familial Barrett Neoplasia

Publications

Created: 9 May 2017, 7:53 a.m.

Panel version: 1.83

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Familial Barrett Neoplasia
Clinvar variants
Variants in VSIG10L
Penetrance
Complete
Publications
Panels with this gene

History Filter Activity

9 May 2017, Gel status: 2

Gene classified by Genomics England curator

Sarah Leigh (Genomics England Curator)

This gene has been classified as Amber List (Moderate Evidence).

9 May 2017, Gel status: 0

Created

Sarah Leigh (Genomics England Curator)

VSIG10L was created by sleigh

9 May 2017, Gel status: 0

Added New Source

Sarah Leigh (Genomics England Curator)

VSIG10L was added to Multiple Tumourspanel. Sources: Literature