STARD7

StAR related lipid transfer domain containing 7
OMIM: 616712, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

No list STARD7 in Mendeliome


Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Removed
  • Expert list
Phenotypes
  • Epilepsy, familial adult myoclonic, 2, 607876
Tags
  • STR

No list STARD7 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Removed
  • Literature
Phenotypes
  • Epilepsy, familial adult myoclonic, 2, 607876
Tags
  • STR

Green STARD7_FAME2_ATTTC STR in Mendeliome


Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Epilepsy, familial adult myoclonic, 2 MIM#607876

Green STARD7_FAME2_ATTTC STR in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Epilepsy, familial adult myoclonic, 2 MIM#607876

Green STARD7_FAME2_ATTTC STR in Repeat Disorders


Version 1.0

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Epilepsy, familial adult myoclonic, 2 MIM#607876
Tags
  • adult-onset