TSR2

TSR2 ribosome maturation factor
OMIM: 300945, ClinGen, DECIPHER

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Red TSR2 in Haematological malignancies


Level 2: Cancer susceptibility
Version 0.148

1 review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • NHS GMS
  • Curated sources
  • Expert Review Red
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, 300946

Red TSR2 in Bone Marrow Failure


Level 2: Haematological disorders
Version 2.9

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • 1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Diamond Blackfan anaemia


    Level 2: Haematological disorders
    Version 2.0

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Mandibulofacial Acrofacial dysostosis


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.9

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Mendeliome


    Version 2.588

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Pierre Robin Sequence


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.5

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Red cell disorders


    Level 2: Haematological disorders
    Version 2.4

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946

    Red TSR2 in Clefting disorders

    Level 3: Dysmorphic disorders
    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.25

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946
    • Cleft palate

    Red TSR2 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 2.7

    1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • BeginNGS
    Phenotypes
    • Diamond-Blackfan anaemia 14 with mandibulofacial dysostosis, MIM# 300946