LAS1L

LAS1 like ribosome biogenesis factor
OMIM: 300964, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red LAS1L in Motor Neurone Disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert Review Red
  • Expert list
  • Melbourne Genomics Health Alliance Complex Neurology Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • congenital lethal motor neuron disease

Green LAS1L in Mendeliome


Version 2.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert Review
  • Victorian Clinical Genetics Services
Phenotypes
  • Wilson-Turner syndrome, MIM# 309585

Green LAS1L in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Genetic Health Queensland
Phenotypes
  • Wilson-Turner syndrome, MIM# 309585

Red LAS1L in Hereditary Neuropathy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review
  • Expert Review Red
  • Expert Review Green
  • Expert Review Red
  • Expert Review
Phenotypes
  • congenital lethal motor neuron disease