Panel 27 · Endocrine & Metabolic Endocrinology

Thyroid Dysgenesis and Dyshormonogenesis Panel

Congenital hypothyroidism due to thyroid dysgenesis or dyshormonogenesis.

Panel number
27 of 58
Clinical category
Endocrine & Metabolic Endocrinology
Genes on this panel
34
Original panel title
Tiroid Disgenezi - Dishormonogenezis Paneli
Source version
PANEL LİSTESİ V9
Requested via
Rare Disease Genomics

Gene content

34 genes

All 34 gene symbols in source order
  • DUOXA1
  • DUOX1
  • DUOX2
  • DUOXA2
  • FOXE1
  • GLI3
  • GNAS
  • HESX1
  • IGSF1
  • IRS4
  • IYD
  • KAT6B
  • LHX3
  • LHX4
  • NKX2-1
  • NKX2-5
  • OTX2
  • PAX8
  • POU1F1
  • PRKAR1A
  • PROP1
  • SECISBP2
  • SLC16A2
  • SLC26A4
  • SLC5A5
  • SOX3
  • TBL1X
  • TG
  • THRA
  • THRB
  • TPO
  • TRHR
  • TSHB
  • TSHR

Gene symbols are reproduced from the department’s current NGS panel source document (PANEL LİSTESİ V9), in source order. No symbol has been added, removed, renamed or expanded, and none has been reconciled against an earlier edition of the catalogue or against an external gene database. Panel titles, gene counts and gene content are published as confirmed by the department. Panel composition may be revised; the version in force at the time of testing applies.