Template:Transcription factor and coregulator deficiencies
{{Navbox
| name = Transcription factor and coregulator deficiencies
| title = Genetic disorders relating to deficiencies of transcription factor or coregulators
| state = {{{state
| listclass = hlist
| group1 = (1) Basic domains
| list1 = {{Navbox|child
| group1 = 1.2
| list1 =
| group2 = 1.3
| list2 =
}}
| group2 = (2) Zinc finger
DNA-binding domains
| list2 = {{Navbox|child
| group1 = 2.1
| list1 =
- (Intracellular receptor): Thyroid hormone resistance
- Androgen insensitivity syndrome
- PAIS
- MAIS
- CAIS
- Kennedy's disease
- PHA1AD pseudohypoaldosteronism
- Estrogen insensitivity syndrome
- X-linked adrenal hypoplasia congenita
- MODY 1
- Familial partial lipodystrophy 3
- SF1 XY gonadal dysgenesis
| group2 = 2.2
| list2 =
| group3 = 2.3
| list3 =
- Greig cephalopolysyndactyly syndrome/Pallister–Hall syndrome
- Denys–Drash syndrome
- Duane-radial ray syndrome
- MODY 7
- MRX 89
- Townes–Brocks syndrome
- Acrocallosal syndrome
- Myotonic dystrophy 2
| group4 = 2.5
| list4 =
}}
| group3 = (3) Helix-turn-helix domains
| list3 = {{Navbox|child
| group1 = 3.1
| list1 =
- ARX
- Ohtahara syndrome
- Lissencephaly X2
- MNX1
- Currarino syndrome
- HOXD13
- SPD1 synpolydactyly
- PDX1
- MODY 4
- LMX1B
- Nail–patella syndrome
- MSX1
- Tooth and nail syndrome
- OFC5
- PITX2
- Axenfeld syndrome 1
- POU4F3
- DFNA15
- POU3F4
- DFNX2
- ZEB1
- Posterior polymorphous corneal dystrophy
- Fuchs' dystrophy 3
- ZEB2
- Mowat–Wilson syndrome
| group2 = 3.2
| list2 =
- PAX2
- Papillorenal syndrome
- PAX3
- Waardenburg syndrome 1&3
- PAX4
- MODY 9
- PAX6
- Gillespie syndrome
- Coloboma of optic nerve
- PAX8
- Congenital hypothyroidism 2
- PAX9
- STHAG3
| group3 = 3.3
| list3 =
- FOXC1
- Axenfeld syndrome 3
- Iridogoniodysgenesis, dominant type
- FOXC2
- Lymphedema–distichiasis syndrome
- FOXE1
- Bamforth–Lazarus syndrome
- FOXE3
- Anterior segment mesenchymal dysgenesis
- FOXF1
- ACD/MPV
- FOXI1
- Enlarged vestibular aqueduct
- FOXL2
- Premature ovarian failure 3
- FOXP3
- IPEX
| group4 = 3.5
| list4 =
}}
| group4 = (4) β-Scaffold factors
with minor groove contacts
| list4 = {{Navbox|child
| group1 = 4.2
| list1 =
| group2 = 4.3
| list2 =
| group3 = 4.7
| list3 =
- Campomelic dysplasia
- MODY 3
- MODY 5
- SF1
- SRY XY gonadal dysgenesis
- Premature ovarian failure 7
- SOX10
- Waardenburg syndrome 4c
- Yemenite deaf-blind hypopigmentation syndrome
| group4 = 4.11
| list4 =
}}
| group5 = (0) Other transcription factors
| list5 = {{Navbox|child
| group1 = 0.6
| list1 =
}}
| group6 = Ungrouped
| list6 =
- TCF4
- Pitt–Hopkins syndrome
- ZFP57
- TNDM1
- TP63
- Rapp–Hodgkin syndrome/Hay–Wells syndrome/Ectrodactyly–ectodermal dysplasia–cleft syndrome 3/Limb–mammary syndrome/OFC8
| group7 = Transcription coregulators
| list7 = {{Navbox|child
| group1 = Coactivator:
| list1 =
| group2 = Corepressor:
| list2 =
}}
}}
{{collapsible option}}
Category:Transcription factor deficiencies
Category:Genetic disease and disorder templates by mechanism