PRDM13

PR/SET domain 13
OMIM: 616741, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green PRDM13 in Cerebellar and Pontocerebellar Hypoplasia


Level 2: Neurology and neurodevelopmental disorders
Version 1.65

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pontocerebellar hypoplasia, type 17, MIM# 619909
  • Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761

Amber PRDM13 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761
Tags
  • founder

Green PRDM13 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Chorioretinal atrophy, progressive bifocal, MIM# 600790
  • Pontocerebellar hypoplasia, type 17, MIM# 619909
  • Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 61976
Tags
  • SV/CNV
  • 5'UTR
  • founder

Green PRDM13 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pontocerebellar hypoplasia, type 17, MIM# 619909
  • Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761
Tags
  • founder

Green PRDM13 in Macular Dystrophy/Stargardt Disease


Level 2: Ophthalmological disorders
Version 0.45

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Macular dystrophy, North Carolina type, MIM#136550
    • Retinal dystrophy
    • Chorioretinal atrophy, progressive bifocal, MIM# 600790
    Tags
    • SV/CNV
    • 5'UTR