Ciliopathies (Homo sapiens)

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1(3) BrainOuter dynein arm,inner dynein armBasal bodyPlasma membraneCiliopathy proteins:Motility apparatus (1),(10)Motile cilium structureCentral pair(1) Cilia motility, respiratory, brain,heart, organ placement, spermOther: cytosol, Golgi, nucleus, etc.Disease groups: (1),(2),(3),(4),(5),(6),(7),(8)Cilium tip Disease groups: (2),(3),(8)INV compartment Disease groups: (2),(5)Transcription factorDisease groups: (3),(4)Centriole or basal bodyDisease groups: (2),(3),(4),(5),(6),(7),(8),(9),(10)Axoneme and signallingDisease groups: (2),(3),(4),(5),(6),(7),(8),(9),(10)GeneProductGeneProductGeneProductGeneProductGLI2ADCY6ANKS3DCDC2EFHC1C21orf2C2orf71CNGB1CNGA1CEP41ANKS6PKD1PKD2SMOPIK3R4OCRLNEK1LCA5IQCB1INPP5EICKGPR161FLCNUSP9XSDCCAG8RAB23PKHD1PKD1L1CEP104ADCY6GLI3NEK8SUFUKIF7CRXNPHP3INVSEVC2EVCZIC2ALMS1AK7XPNPEP3TBC1D32POMGNT1PIK3R4GLIS2GALNT11DDX59ZNF423Primary ciliary dyskinesia (PCD)Bardet-Biedl syndrome (BBS)Primary ciliary dyskinesia (PCD)Carpenter syndrome (CRPT)Hydrolethalus syndrome (HLS)OMIM:135150 Birt-Hogg-Dube syndromeHoloprosencephaly (HPE)Senior-Loken syndrome (SLSN)OMIM:146510 Pallister-Hall syndrome (PHS)MORM syndromeMeckel syndrome (MKS)Oculocerebrorenal syndrome (OCRL)Hydrolethalus syndrome (HLS)OMIM:309000 Lowe syndrome (OCRL)Joubert syndrome (JBTS)(2) Multi-systemic (primary cilia),brain, kidney, skeleton, eyesOMIM:107200 Anosmia, isolated congenitalPolycystic kidney disease (PKD)Nephronophthisis (NPHP)Retinitis pigmentosa (RP)Cone-rod dysrtophy (CRD)OMIM:155255 MedulloblastomaLeber congenital amaurosis (LCA)OMIM:254770 Juvenile myoclonic epilepsy (JME)(4) Eyes(5) Kidney(6) NoseHearing lossShort-rib thoracic dysplasia (SRTD)Orofaciodigital syndrome (OFD)Jeune asphyxiating thoracic dystrophy (JATD)OMIM:175700 Grieg cephalopolysyndactyly syndromeOMIM:225500 Ellis-van Creveld syndrome (EVC)Situs inversus, heterotaxyCongenital heart disease (CHD)(7) Organ placement, heart(8) Skeleton(9) Ears(10) VariousLethal congenital contracture syndrome (LCCS)Polycystic kidney disease and hepatic diseasePituitary stalk interruption syndrome (PSIS)Male infertilityGeneProductGeneProductGeneProductTULP1OFD1KIAA0556INTUFLCNPLK4PIBF1OCRLNME7HYLS1C21orf2C2CD3CEP104CEP78NEK2KIZFAM161ACSPP1CEP120CEP41CEP19CENPFARL2BPCFAP52NEK9ATXN10CC2D2AOFD1WDPCPTTLL5TOPORSCEP83TUBTAPT1RP2KIAA0586RAB28POC1APOC1BDistal appendageDisease groups: (2),(4),(5),(8),(10)CEP164TTBK2SCLT1Subdistal appendageDisease groups: (2)Transition zoneDisease groups: (1),(2),(4),(5),(8)CEP290CFAP53CCDC28BKIAA0753BBS4TMEM237TMEM231TMEM216TMEM138TMEM107TMEM67TCTN2TMEM17TCTN1SPATA7SDCCAG8RPGRIP1LIQCB1RPGRIP1RP1L1C5orf42TCTN3RP1NPHP4CEP290NPHP1MKS1CC2D2ALCA5B9D2B9D1AHI1Centriolar satellitesDisease groups: (1),(2),(4),(5),(7),(8)Unclear or various localizationDisease groups: (2),(4),(5),(7),(8),(10)RSPH1GAS8LRRC6NME9MCIDASDNAL1DNAAF4CCDC151DNAAF5DNAI2CCNODNAH6DNAJB13PIH1D3CCDC40HYDINCCDC103DNAH11ARMC4ZMYND10TTC25DRC1SPAG1RSPH3CCDC114CCDC39CCDC65DNAAF5RSPH4ARSPH9DNAAF1C21orf59DNAI1DNAAF2DNAAF3Nexin-dynein regulatory complexRadial spokeCytoplasmRegulation of centrioles and transcription in multiciliated cellsNon-motile cilium structureIFT subcomplex B Disease groups: (2),(4),(5),(8)IFT cilia regulators Disease groups: (2),(4),(8)IFT dynein subunits Disease groups: (8)LIFT Disease groups: (2),(4)WDR60UNC119IFT172ARL3BBS2TTC21BWDR34CCNQWDR19DYNC2LI1IFT27BBS10CEP290MKS1BBS12MAKSDCCAG8ARL6BBS7BBIP1IFT43LZTFL1IFT122MKKSWDR35BBS4ICKC8orf37TRAF3IP1DYNC2H1IFT57BBS1RP2BBS5TCTEX1D2IFT81TTC8IFT80BBS9WDPCPTRIM32CLUAP1PDE6DIFT52ARL13BIFT140IFT kinesin subunitsNo known associations with ciliopathiesIFT subcomplex ADisease groups: (2),(4),(5),(8)BBS proteinsBBSome (IFT-associated) Disease groups: (2),(4)BBSome regulators Disease groups: (2),(4),(5),(8)Plasma membraneBasal bodyGeneProduct


Description

Incomplete pathway Taken from Genes and molecular pathways underpinning ciliopathies by Jeremy F. Reiter and Michel R. Leroux [1].

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Ontology Terms

 

Bibliography

  1. Reiter JF, Leroux MR; ''Genes and molecular pathways underpinning ciliopathies.''; Nat Rev Mol Cell Biol, 2017 PubMed Europe PMC Scholia

History

View all...
CompareRevisionActionTimeUserComment
128947view12:20, 24 February 2024EweitzSoften disease colors
128942view01:26, 24 February 2024EweitzFix typo, add conventional space
128941view01:24, 24 February 2024EweitzFix typo, remove duplicate disease node
128940view01:22, 24 February 2024EweitzOntology Term : 'infertility' added !
128939view01:22, 24 February 2024EweitzOntology Term : 'male infertility' added !
128938view01:22, 24 February 2024EweitzOntology Term : 'lethal congenital contracture syndrome' added !
128937view01:21, 24 February 2024EweitzOntology Term : 'Birt-Hogg-Dube syndrome' added !
128936view01:21, 24 February 2024EweitzOntology Term : 'sensorineural hearing loss' added !
128935view01:19, 24 February 2024EweitzOntology Term : 'orofaciodigital syndrome' added !
128934view01:19, 24 February 2024EweitzOntology Term : 'asphyxiating thoracic dystrophy' added !
128933view01:19, 24 February 2024EweitzOntology Term : 'Greig cephalopolysyndactyly syndrome' added !
128932view01:18, 24 February 2024EweitzOntology Term : 'Ellis-Van Creveld syndrome' added !
128931view01:17, 24 February 2024EweitzOntology Term : 'congenital heart disease' added !
128930view01:16, 24 February 2024EweitzOntology Term : 'polycystic kidney disease' added !
128929view01:16, 24 February 2024EweitzOntology Term : 'nephronophthisis' added !
128928view01:16, 24 February 2024EweitzOntology Term : 'retinitis pigmentosa' added !
128927view01:15, 24 February 2024EweitzOntology Term : 'cone-rod dystrophy' added !
128926view01:15, 24 February 2024EweitzOntology Term : 'Leber congenital amaurosis' added !
128925view01:15, 24 February 2024EweitzOntology Term : 'medulloblastoma' added !
128924view01:14, 24 February 2024EweitzOntology Term : 'juvenile myoclonic epilepsy' added !
128923view01:14, 24 February 2024EweitzOntology Term : 'holoprosencephaly' added !
128922view01:14, 24 February 2024EweitzOntology Term : 'Senior-Loken syndrome' added !
128921view01:13, 24 February 2024EweitzOntology Term : 'Pallister-Hall syndrome' added !
128920view01:13, 24 February 2024EweitzOntology Term : 'Meckel syndrome' added !
128919view01:12, 24 February 2024EweitzOntology Term : 'oculocerebrorenal syndrome' added !
128918view01:11, 24 February 2024EweitzOntology Term : 'Joubert syndrome' added !
128917view01:11, 24 February 2024EweitzOntology Term : 'hydrolethalus syndrome' added !
128916view01:11, 24 February 2024EweitzOntology Term : 'Carpenter syndrome' added !
128915view01:10, 24 February 2024EweitzOntology Term : 'Bardet-Biedl syndrome' added !
128914view01:10, 24 February 2024EweitzOntology Term : 'primary ciliary dyskinesia' added !
128230view13:36, 29 January 2024EweitzSoften disease color
110008view18:16, 12 April 2020AlexanderPicoOntology Term : 'disease pathway' added !
110007view18:05, 12 April 2020AlexanderPicoModified description
110006view17:59, 12 April 2020AlexanderPicochanged interactions into graphical lines; removed stray gene produce nodes
109918view17:03, 6 April 2020KhanspersOntology Term : 'ciliopathy' added !
109093view04:45, 17 February 2020RleeDownsized diagram 3
109089view02:16, 17 February 2020RleeUpdated graphics: added disease gropu boxes and added shapes to 3rd diagram
109088view00:48, 17 February 2020RleeImproved graphic: added colour to GeneProduct nodes
109028view04:55, 14 February 2020RleeMade semi-circles (arcs) transparent, graphical improvement.
109027view04:53, 14 February 2020RleeMade semi-circles (arcs) transparent.
109026view04:51, 14 February 2020RleeUpdated diagrams.
109025view04:43, 14 February 2020RleeUpdated diagrams.
109020view03:23, 14 February 2020RleeUpdated diagrams.
109019view02:59, 14 February 2020RleeUpdated diagrams.
109016view02:26, 14 February 2020RleeUpdated diagrams.
109015view02:05, 14 February 2020RleeModified description
109014view00:09, 14 February 2020RleeModified description
109013view00:01, 14 February 2020RleeModified description
109012view23:59, 13 February 2020RleeNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
ADCY6GeneProductENSG00000174233 (Ensembl)
AHI1GeneProductENSG00000135541 (Ensembl)
AK7GeneProductENSG00000140057 (Ensembl)
ALMS1GeneProductENSG00000116127 (Ensembl)
ANKS3GeneProductENSG00000168096 (Ensembl)
ANKS6GeneProductENSG00000165138 (Ensembl)
ARL13BGeneProductENSG00000169379 (Ensembl)
ARL2BPGeneProductENSG00000102931 (Ensembl)
ARL3GeneProductENSG00000138175 (Ensembl)
ARL6GeneProductENSG00000113966 (Ensembl)
ARMC4GeneProductENSG00000169126 (Ensembl)
ATXN10GeneProductENSG00000130638 (Ensembl)
B9D1GeneProductENSG00000108641 (Ensembl)
B9D2GeneProductENSG00000123810 (Ensembl)
BBIP1GeneProductENSG00000214413 (Ensembl)
BBS10GeneProductENSG00000179941 (Ensembl)
BBS12GeneProductENSG00000181004 (Ensembl)
BBS1GeneProductENSG00000174483 (Ensembl)
BBS2GeneProductENSG00000125124 (Ensembl)
BBS4GeneProductENSG00000140463 (Ensembl)
BBS5GeneProductENSG00000163093 (Ensembl)
BBS7GeneProductENSG00000138686 (Ensembl)
BBS9GeneProductENSG00000122507 (Ensembl)
C21orf2GeneProductENSG00000160226 (Ensembl)
C21orf59GeneProductENSG00000159079 (Ensembl)
C2CD3GeneProductENSG00000168014 (Ensembl)
C2orf71GeneProductENSG00000179270 (Ensembl)
C5orf42GeneProductENSG00000197603 (Ensembl)
C8orf37GeneProductENSG00000156172 (Ensembl)
CC2D2AGeneProductENSG00000048342 (Ensembl)
CCDC103GeneProductENSG00000167131 (Ensembl)
CCDC114GeneProductENSG00000105479 (Ensembl)
CCDC151GeneProductENSG00000198003 (Ensembl)
CCDC28BGeneProductENSG00000160050 (Ensembl)
CCDC39GeneProductENSG00000284862 (Ensembl)
CCDC40GeneProductENSG00000141519 (Ensembl)
CCDC65GeneProductENSG00000139537 (Ensembl)
CCNOGeneProductENSG00000152669 (Ensembl)
CCNQGeneProductENSG00000262919 (Ensembl)
CENPFGeneProductENSG00000117724 (Ensembl)
CEP104GeneProductENSG00000116198 (Ensembl)
CEP120GeneProductENSG00000168944 (Ensembl)
CEP164GeneProductENSG00000110274 (Ensembl)
CEP19GeneProductENSG00000174007 (Ensembl)
CEP290GeneProductENSG00000198707 (Ensembl)
CEP41GeneProductENSG00000106477 (Ensembl)
CEP78GeneProductENSG00000148019 (Ensembl)
CEP83GeneProductENSG00000173588 (Ensembl)
CFAP52GeneProductENSG00000166596 (Ensembl)
CFAP53GeneProductENSG00000172361 (Ensembl)
CLUAP1GeneProductENSG00000103351 (Ensembl)
CNGA1GeneProductENSG00000198515 (Ensembl)
CNGB1GeneProductENSG00000070729 (Ensembl)
CRXGeneProductENSG00000105392 (Ensembl)
CSPP1GeneProductENSG00000104218 (Ensembl)
DCDC2GeneProductENSG00000146038 (Ensembl)
DDX59GeneProductENSG00000118197 (Ensembl)
DNAAF1GeneProductENSG00000154099 (Ensembl)
DNAAF2GeneProductENSG00000165506 (Ensembl)
DNAAF3GeneProductENSG00000167646 (Ensembl)
DNAAF4GeneProductENSG00000256061 (Ensembl)
DNAAF5GeneProductENSG00000164818 (Ensembl)
DNAH11GeneProductENSG00000105877 (Ensembl)
DNAH6GeneProductENSG00000115423 (Ensembl)
DNAI1GeneProductENSG00000122735 (Ensembl)
DNAI2GeneProductENSG00000171595 (Ensembl)
DNAJB13GeneProductENSG00000187726 (Ensembl)
DNAL1GeneProductENSG00000119661 (Ensembl)
DRC1GeneProductENSG00000157856 (Ensembl)
DYNC2H1GeneProductENSG00000187240 (Ensembl)
DYNC2LI1GeneProductENSG00000138036 (Ensembl)
EFHC1GeneProductENSG00000096093 (Ensembl)
EVC2GeneProductENSG00000173040 (Ensembl)
EVCGeneProductENSG00000072840 (Ensembl)
FAM161AGeneProductENSG00000170264 (Ensembl)
FLCNGeneProductENSG00000154803 (Ensembl)
GALNT11GeneProductENSG00000178234 (Ensembl)
GAS8GeneProductENSG00000141013 (Ensembl)
GLI2GeneProductENSG00000074047 (Ensembl)
GLI3GeneProductENSG00000106571 (Ensembl)
GLIS2GeneProductENSG00000126603 (Ensembl)
GPR161GeneProductENSG00000143147 (Ensembl)
GeneProductGeneProduct
HYDINGeneProductENSG00000157423 (Ensembl)
HYLS1GeneProductENSG00000198331 (Ensembl)
ICKGeneProductENSG00000112144 (Ensembl)
IFT122GeneProductENSG00000163913 (Ensembl)
IFT140GeneProductENSG00000187535 (Ensembl)
IFT172GeneProductENSG00000138002 (Ensembl)
IFT27GeneProductENSG00000100360 (Ensembl)
IFT43GeneProductENSG00000119650 (Ensembl)
IFT52GeneProductENSG00000101052 (Ensembl)
IFT57GeneProductENSG00000114446 (Ensembl)
IFT80GeneProductENSG00000068885 (Ensembl)
IFT81GeneProductENSG00000122970 (Ensembl)
INPP5EGeneProductENSG00000148384 (Ensembl)
INTUGeneProductENSG00000164066 (Ensembl)
INVSGeneProductENSG00000119509 (Ensembl)
IQCB1GeneProductENSG00000173226 (Ensembl)
KIAA0556GeneProductENSG00000047578 (Ensembl)
KIAA0586GeneProductENSG00000100578 (Ensembl)
KIAA0753GeneProductENSG00000198920 (Ensembl)
KIF7GeneProductENSG00000166813 (Ensembl)
KIZGeneProductENSG00000088970 (Ensembl)
LCA5GeneProductENSG00000135338 (Ensembl)
LRRC6GeneProductENSG00000129295 (Ensembl)
LZTFL1GeneProductENSG00000163818 (Ensembl)
MAKGeneProductENSG00000111837 (Ensembl)
MCIDASGeneProductENSG00000234602 (Ensembl)
MKKSGeneProductENSG00000125863 (Ensembl)
MKS1GeneProductENSG00000011143 (Ensembl)
NEK1GeneProductENSG00000137601 (Ensembl)
NEK2GeneProductENSG00000117650 (Ensembl)
NEK8GeneProductENSG00000160602 (Ensembl)
NEK9GeneProductENSG00000119638 (Ensembl)
NME7GeneProductENSG00000143156 (Ensembl)
NME9GeneProductENSG00000181322 (Ensembl)
NPHP1GeneProductENSG00000144061 (Ensembl)
NPHP3GeneProductENSG00000113971 (Ensembl)
NPHP4GeneProductENSG00000131697 (Ensembl)
OCRLGeneProductENSG00000122126 (Ensembl)
OFD1GeneProductENSG00000046651 (Ensembl)
PDE6DGeneProductENSG00000156973 (Ensembl)
PIBF1GeneProductENSG00000083535 (Ensembl)
PIH1D3GeneProductENSG00000080572 (Ensembl)
PIK3R4GeneProductENSG00000196455 (Ensembl)
PKD1GeneProductENSG00000008710 (Ensembl)
PKD1L1GeneProductENSG00000158683 (Ensembl)
PKD2GeneProductENSG00000118762 (Ensembl)
PKHD1GeneProductENSG00000170927 (Ensembl)
PLK4GeneProductENSG00000142731 (Ensembl)
POC1AGeneProductENSG00000164087 (Ensembl)
POC1BGeneProductENSG00000139323 (Ensembl)
POMGNT1GeneProductENSG00000085998 (Ensembl)
RAB23GeneProductENSG00000112210 (Ensembl)
RAB28GeneProductENSG00000157869 (Ensembl)
RP1GeneProductENSG00000104237 (Ensembl)
RP1L1GeneProductENSG00000183638 (Ensembl)
RP2GeneProductENSG00000102218 (Ensembl)
RPGRIP1GeneProductENSG00000092200 (Ensembl)
RPGRIP1LGeneProductENSG00000103494 (Ensembl)
RSPH1GeneProductENSG00000160188 (Ensembl)
RSPH3GeneProductENSG00000130363 (Ensembl)
RSPH4AGeneProductENSG00000111834 (Ensembl)
RSPH9GeneProductENSG00000172426 (Ensembl)
SCLT1GeneProductENSG00000151466 (Ensembl)
SDCCAG8GeneProductENSG00000054282 (Ensembl)
SMOGeneProductENSG00000128602 (Ensembl)
SPAG1GeneProductENSG00000104450 (Ensembl)
SPATA7GeneProductENSG00000042317 (Ensembl)
SUFUGeneProductENSG00000107882 (Ensembl)
TAPT1GeneProductENSG00000169762 (Ensembl)
TBC1D32GeneProductENSG00000146350 (Ensembl)
TCTEX1D2GeneProductENSG00000213123 (Ensembl)
TCTN1GeneProductENSG00000204852 (Ensembl)
TCTN2GeneProductENSG00000168778 (Ensembl)
TCTN3GeneProductENSG00000119977 (Ensembl)
TMEM107GeneProductENSG00000179029 (Ensembl)
TMEM138GeneProductENSG00000149483 (Ensembl)
TMEM17GeneProductENSG00000186889 (Ensembl)
TMEM216GeneProductENSG00000187049 (Ensembl)
TMEM231GeneProductENSG00000205084 (Ensembl)
TMEM237GeneProductENSG00000155755 (Ensembl)
TMEM67GeneProductENSG00000164953 (Ensembl)
TOPORSGeneProductENSG00000197579 (Ensembl)
TRAF3IP1GeneProductENSG00000204104 (Ensembl)
TRIM32GeneProductENSG00000119401 (Ensembl)
TTBK2GeneProductENSG00000128881 (Ensembl)
TTC21BGeneProductENSG00000123607 (Ensembl)
TTC25GeneProductENSG00000204815 (Ensembl)
TTC8GeneProductENSG00000165533 (Ensembl)
TTLL5GeneProductENSG00000119685 (Ensembl)
TUBGeneProductENSG00000166402 (Ensembl)
TULP1GeneProductENSG00000112041 (Ensembl)
UNC119GeneProductENSG00000109103 (Ensembl)
USP9XGeneProductENSG00000124486 (Ensembl)
WDPCPGeneProductENSG00000143951 (Ensembl)
WDR19GeneProductENSG00000157796 (Ensembl)
WDR34GeneProductENSG00000119333 (Ensembl)
WDR35GeneProductENSG00000118965 (Ensembl)
WDR60GeneProductENSG00000126870 (Ensembl)
XPNPEP3GeneProductENSG00000196236 (Ensembl)
ZIC2GeneProductENSG00000043355 (Ensembl)
ZMYND10GeneProductENSG00000004838 (Ensembl)
ZNF423GeneProductENSG00000102935 (Ensembl)

Annotated Interactions

No annotated interactions

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