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|autocollapse}}}

| listclass = hlist

| group1 = (1) Basic domains

| list1 = {{Navbox|child

| group1 = 1.2

| list1 =

• Feingold syndrome
• Saethre–Chotzen syndrome

| group2 = 1.3

| list2 =

• Tietz syndrome

}}

| 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 =

• Barakat syndrome
• Tricho–rhino–phalangeal syndrome

| 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 =

• Autoimmune polyendocrine syndrome type 1

}}

| 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 =

• IRF6
• Van der Woude syndrome
• Popliteal pterygium syndrome

}}

| group4 = (4) β-Scaffold factors
with minor groove contacts

| list4 = {{Navbox|child

| group1 = 4.2

| list1 =

• Hyperimmunoglobulin E syndrome

| group2 = 4.3

| list2 =

• Holt–Oram syndrome
• Li–Fraumeni syndrome
• Ulnar–mammary syndrome

| 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 =

• Cleidocranial dysostosis

}}

| group5 = (0) Other transcription factors

| list5 = {{Navbox|child

| group1 = 0.6

| list1 =

• Kabuki syndrome

}}

| 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 =

• CREBBP
• Rubinstein–Taybi syndrome

| group2 = Corepressor:

| list2 =

• HR (Atrichia with papular lesions)

}}

}}

{{collapsible option}}

Category:Transcription factor deficiencies

Category:Genetic disease and disorder templates by mechanism