Description
This panel was developed and is maintained by VCGS. It contains conditions caused by defects in the motile cilia, primarily those presenting with respiratory phenotypes. It also contains a small number of other genes that cause conditions with significant phenotypic overlap.

This panel has been compared against the Genomics England PanelApp 'Respiratory Ciliopathies including non-CF bronchiectasis' panel V1.3, with all discrepancies resolved and reciprocal feedback provided to Genomics England.

12 reviewers

  • Sebastian Lunke (Victorian Clinical Genetics Services)

  • Alison Yeung (Victorian Clinical Genetics Services)

  • Belinda Chong (Victorian Clinical Genetics Services)

  • Teresa Zhao (Victorian Clinical Genetics Services)

  • Chirag Patel (Genetic Health Queensland)

  • Achchuthan Shanmugasundram (Genomics England)

  • Ain Roesley (Victorian Clinical Genetics Services)

  • Elena Savva (Victorian Clinical Genetics Services)

  • Crystle Lee (Victorian Clinical Genetics Services)

  • Sangavi Sivagnanasundram (Melbourne Health)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

  • Chern Lim (Victorian Clinical Genetics Services)

74 Entities

74 reviewed, 50 green

List Entity Reviews Mode of inheritance Details
74 Entitiess
Green Green List (high evidence)
AGR2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Recurrent respiratory infections and failure to thrive with or without diarrhea (RIFTD), MIM#620233
Tags
Green Green List (high evidence)
ARMC4
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 23, MIM# 615451
Tags
  • new gene name
Green Green List (high evidence)
C11orf70
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Ciliary dyskinesia, primary, 38 618063
Tags
  • new gene name
Green Green List (high evidence)
C21orf59
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 26, MIM# 615500
Tags
  • founder
  • new gene name
Green Green List (high evidence)
CCDC103
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 17, MIM# 614679
Tags
  • founder
Green Green List (high evidence)
CCDC114
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 20, MIM# 615067
Tags
  • new gene name
Green Green List (high evidence)
CCDC151
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 30, MIM# 616037
Tags
  • new gene name
Green Green List (high evidence)
CCDC39
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 14, MIM# 613807
Tags
Green Green List (high evidence)
CCDC40
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 15, MIM#613808
Tags
Green Green List (high evidence)
CCDC65
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 27, MIM# 615504
Tags
  • founder
Green Green List (high evidence)
CCNO
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 29, MIM# 615872
Tags
Green Green List (high evidence)
CFAP43
2 reviews
1 green
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Hydrocephalus, normal pressure, 1 236690
  • Spermatogenic failure 19 617592
Tags
Green Green List (high evidence)
CFAP53
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Heterotaxy, visceral, 6, autosomal recessive 614779
Tags
Green Green List (high evidence)
CFTR
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Cystic fibrosis
  • bronchiectasis
Tags
Green Green List (high evidence)
DAW1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Primary ciliary dyskinesia, with or without heterotaxy, MIM#620570
Tags
Green Green List (high evidence)
DNAAF1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 13, MIM# 613193
Tags
Green Green List (high evidence)
DNAAF2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 10, MIM# 612518
Tags
Green Green List (high evidence)
DNAAF3
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 2, MIM# 606763
Tags
Green Green List (high evidence)
DNAAF4
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 25, MIM# 615482
Tags
  • founder
  • SV/CNV
Green Green List (high evidence)
DNAAF5
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 18, MIM# 614874
Tags
Green Green List (high evidence)
DNAH11
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 7, with or without situs inversus, MIM#611884
Tags
Green Green List (high evidence)
DNAH5
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 3, with or without situs inversus (MIM #608644)
Tags
Green Green List (high evidence)
DNAH7
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Primary ciliary dyskinesia, MONDO:0016575, DNAH7-related
Tags
Green Green List (high evidence)
DNAH9
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 40, MIM# 618300
Tags
Green Green List (high evidence)
DNAI1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 1, with or without situs inversus, MIM# 244400
Tags
Green Green List (high evidence)
DNAI2
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 9, with or without situs inversus, MIM# 612444
Tags
Green Green List (high evidence)
DNAJB13
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 34 617091
Tags
Green Green List (high evidence)
DRC1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 21, MIM# 615294
Tags
  • SV/CNV
Green Green List (high evidence)
EFCAB1
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 53, MIM# 620642
Tags
  • new gene name
Green Green List (high evidence)
FOXJ1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 43, MIM# 618699
  • hydrocephalus
  • chronic destructive airway disease
  • randomization of left/right body asymmetry
Tags
Green Green List (high evidence)
GAS8
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 33, mIM# 616726
Tags
Green Green List (high evidence)
HYDIN
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 5 (MIM#608647)
Tags
Green Green List (high evidence)
LRRC56
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Ciliary dyskinesia, primary, 39 618254
Tags
Green Green List (high evidence)
LRRC6
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 19, MIM# 614935
Tags
Green Green List (high evidence)
MCIDAS
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 42 (MIM#618695)
Tags
Green Green List (high evidence)
NEK10
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Ciliary dyskinesia, primary, 44, MIM# 618781
  • Bronchiectasis
Tags
Green Green List (high evidence)
OFD1
2 reviews
2 green
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Joubert syndrome 10, MIM 300804
  • Orofaciodigital syndrome I, MIM 311200
  • Simpson-Golabi-Behmel syndrome, type 2, MIM 300209
  • Primary ciliary dyskinesia
Tags
Green Green List (high evidence)
PIH1D3
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 36, X-linked (MIM#300991)
Tags
Green Green List (high evidence)
RPGR
1 review
1 green
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Retinitis pigmentosa, X-linked, and sinorespiratory infections, with or without deafness, MIM# 300455
Tags
Green Green List (high evidence)
RSPH1
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 24 (MIM#615481)
Tags
Green Green List (high evidence)
RSPH3
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 32 (MIM#616481)
Tags
Green Green List (high evidence)
RSPH4A
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 11 (MIM#612649)
Tags
Green Green List (high evidence)
RSPH9
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 12 (MIM#612650)
Tags
Green Green List (high evidence)
SCNN1G
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Bronchiectasis with or without elevated sweat chloride 3, MIM# 613071
Tags
Green Green List (high evidence)
SPAG1
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 28 (MIM#615505)
Tags
Green Green List (high evidence)
TP73
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 47, and lissencephaly, MIM#619466
Tags
Green Green List (high evidence)
TTC12
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ciliary dyskinesia
Tags
Green Green List (high evidence)
TTC25
3 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review
  • Expert Review Green
Phenotypes
  • Ciliary dyskinesia, primary, 35 (MIM#617092)
Tags
  • new gene name
Green Green List (high evidence)
TUBB4B
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Primary ciliary dyskinesia, MONDO:0016575, TUBB4B-related
Tags
Green Green List (high evidence)
ZMYND10
2 reviews
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 22, MIM#615444
Tags
Amber Amber List (moderate evidence)
CFAP57
2 reviews
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Van der Woude Syndrome
  • Primary ciliary dyskinesia
Tags
Amber Amber List (moderate evidence)
CFAP74
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Primary ciliary dyskinesia
  • infertility
Tags
Amber Amber List (moderate evidence)
DNAH1
2 reviews
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • ?Ciliary dyskinesia, primary, 37 617577
  • Spermatogenic failure 18 617576
Tags
Amber Amber List (moderate evidence)
DNAH6
2 reviews
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Heterotaxy, Azoospermia
Tags
Amber Amber List (moderate evidence)
DNAH8
2 reviews
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Spermatogenic failure 46, MIM#619095
  • Asthenozoospermia
  • primary ciliary dyskinesia
Tags
Amber Amber List (moderate evidence)
DNAL1
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 16, MIM# 614017
Tags
  • founder
Amber Amber List (moderate evidence)
GAS2L2
2 reviews
1 green 1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 41 (MIM # 618449)
Tags
Amber Amber List (moderate evidence)
NFKB1
2 reviews
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Immunodeficiency, common variable, 12 616576
Tags
Amber Amber List (moderate evidence)
NFKB2
2 reviews
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Immunodeficiency, common variable, 10 615577
Tags
Amber Amber List (moderate evidence)
NME5
3 reviews
1 green 1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Primary ciliary dyskinesia
Tags
Amber Amber List (moderate evidence)
PIK3CD
2 reviews
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Immunodeficiency 14 615513
Tags
Amber Amber List (moderate evidence)
PIK3R1
2 reviews
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • ?Agammaglobulinemia 7, autosomal recessive 615214
  • Immunodeficiency 36 616005
  • SHORT syndrome 269880
Tags
Amber Amber List (moderate evidence)
SCNN1A
2 reviews
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review
  • Expert Review Amber
Phenotypes
  • Bronchiectasis with or without elevated sweat chloride 2 (MIM#613021)
  • MONDO:0013087
Tags
Amber Amber List (moderate evidence)
SCNN1B
2 reviews
1 green
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review
  • Expert Review Amber
Phenotypes
  • Bronchiectasis with or without elevated sweat chloride 1 (MIM#211400)
Tags
Amber Amber List (moderate evidence)
SPEF2
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Spermatogenic failure 43, MIM#618751
  • Primary ciliary dyskinesia-like phenotype
Tags
Red Red List (low evidence)
AKNA
2 reviews
2 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Primary ciliary dyskinesia, MONDO:0016575, AKNA-related
Tags
Red Red List (low evidence)
BRWD1
2 reviews
1 green 1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ciliary dyskinesia, primary, 51, MIM# 620438
Tags
  • disputed
Red Red List (low evidence)
CFAP221
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Primary ciliary dyskinesia
Tags
Red Red List (low evidence)
CFAP54
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hydrocephalus, male infertility, mucus accumulation
Tags
Red Red List (low evidence)
GOLGA3
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Primary ciliary dyskinesia
Tags
Red Red List (low evidence)
ITCH
2 reviews
2 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Autoimmune disease, multisystem, with facial dysmorphism 613385
  • primary ciliary dyskinesia
Tags
Red Red List (low evidence)
NME8
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Ciliary dyskinesia, primary, 6, MIM# 610852
Tags
Red Red List (low evidence)
STK36
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Red
Phenotypes
  • Ciliary dyskinesia, primary, 46, MIM# 619436
Tags
No list No list
DNAH17
1 review
1 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
Phenotypes
  • spermatogenic failure 39 (MONDO:0032845)
Tags

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