SLC25A11

solute carrier family 25 member 11
OMIM: 604165, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC25A11 in Incidentalome


Version 0.430

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review
  • Literature
  • Expert Review Red
  • Literature
  • Expert Review
  • Expert list
Phenotypes
  • Paragangliomas 6, MONDO:0032767
  • Pheochromocytoma, MONDO:0008233
  • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
  • Pheochromocytoma/paraganglioma syndrome 6, MIM#618464

Red SLC25A11 in Paraganglioma_phaeochromocytoma


Level 2: Cancer Predisposition
Version 1.2

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Expert Review
  • Expert list
Phenotypes
  • Paragangliomas 6, MONDO:0032767
  • Pheochromocytoma, MONDO:0008233
  • Hereditary pheochromocytoma-paraganglioma, MONDO:0017366
  • Pheochromocytoma/paraganglioma syndrome 6, MIM#618464