Description
This panel contains genes that cause schwannomatosis or a differential diagnosis of the disorder. It is maintained by RMH.

3 reviewers

  • Andrew Fennell (Monash Genetics)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

8 Entities

4 reviewed, 6 green

List Entity Reviews Mode of inheritance Details
8 Entitiess
Green Green List (high evidence)
LZTR1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • {Schwannomatosis-2, susceptibility to} MIM#615670
Tags
Green Green List (high evidence)
NF1
0 reviews
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Neurofibromatosis, type 1 MIM#162200
Tags
Green Green List (high evidence)
NF2
0 reviews
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Neurofibromatosis, type 2 MIM#101000
Tags
Green Green List (high evidence)
PRKAR1A
0 reviews
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Carney complex, type 1 MIM#160980
Tags
Green Green List (high evidence)
SMARCB1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • {Schwannomatosis-1, susceptibility to} MIM#162091
Tags
Green Green List (high evidence)
SMARCE1
0 reviews
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • {Meningioma, familial, susceptibility to} MIM#607174
Tags
Amber Amber List (moderate evidence)
SUFU
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • {Meningioma, familial, susceptibility to} MIM#607174
  • Basal cell nevus syndrome MIM#109400
Tags
Red Red List (low evidence)
DGCR8
2 reviews
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Early-onset multinodular goiter and schwannomatosis
Tags

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