hu.MAP 3.0: Complex View
Human Protein Complex Map
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Complex: huMAP3_03435.1
Confidence: Extremely High  
ProteinsGenename | Protein Name | Uniprot Annotation Score | Links |
---|---|---|---|
IFT140 | Intraflagellar transport protein 140 homolog (WD and tetratricopeptide repeats protein 2) | 5 | UniProt   NCBI |
IFT43 | Intraflagellar transport protein 43 homolog | 5 | UniProt   NCBI |
WDR35 | WD repeat-containing protein 35 (Intraflagellar transport protein 121 homolog) | 5 | UniProt   NCBI |
IFT122 | Intraflagellar transport protein 122 homolog (WD repeat-containing protein 10) (WD repeat-containing protein 140) | 5 | UniProt   NCBI |
WDR19 | WD repeat-containing protein 19 (Intraflagellar transport 144 homolog) | 5 | UniProt   NCBI |
IFTAP | Intraflagellar transport-associated protein (Protein HEPIS) | 3 | UniProt   NCBI |
Enrichments
Term ID | Corrected Pval | Fraction Complex Coverage | Proteins | Term Name |
---|---|---|---|---|
  GO:0030991 | 3.2413958192e-13 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | intraciliary transport particle A |
  CORUM:6585 | 4.80104919782e-12 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Intraflagellar transport complex A |
  WP:WP4532 | 6.24974716144e-12 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Intraflagellar transport proteins binding to dynein |
  GO:0035721 | 6.95001783241e-11 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | intraciliary retrograde transport |
  REAC:R-HSA-5620924 | 4.65360810562e-10 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Intraflagellar transport |
  WP:WP5234 | 1.42623518968e-09 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Bardet Biedl syndrome |
  GO:0030990 | 1.81606603046e-09 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | intraciliary transport particle |
  HP:0008905 | 4.92898512047e-09 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Rhizomelia |
  WP:WP4536 | 5.23603068389e-09 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Genes related to primary cilium development based on CRISPR |
  HP:0008873 | 4.29803835863e-08 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Disproportionate short-limb short stature |
  GO:0042073 | 4.58614910437e-08 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | intraciliary transport |
  WP:WP4803 | 5.54557903312e-08 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Ciliopathies |
  GO:0097542 | 6.58565753718e-08 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | ciliary tip |
  HP:0000774 | 9.65286586915e-08 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Narrow chest |
  HP:0003498 | 1.2126052463e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Disproportionate short stature |
  HP:0005257 | 2.27149801615e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Thoracic hypoplasia |
  REAC:R-HSA-5617833 | 3.74471976961e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Cilium Assembly |
  HP:0010306 | 5.52747893676e-07 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Short thorax |
  HP:0000691 | 6.14182442931e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Microdontia |
  HP:0009803 | 7.42377744679e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Short phalanx of finger |
  HP:0000679 | 7.46166611169e-07 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Taurodontia |
  HP:0011071 | 7.46166611169e-07 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal permanent molar morphology |
  HP:0001363 | 7.65678883854e-07 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Craniosynostosis |
  HP:0011070 | 9.00661990159e-07 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal molar morphology |
  HP:0011077 | 9.86331068136e-07 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormality of molar |
  HP:0006479 | 1.07796447757e-06 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal dental pulp morphology |
  HP:0006486 | 1.07796447757e-06 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal dental root morphology |
  HP:0000268 | 1.09377697467e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Dolichocephaly |
  HP:0000269 | 1.28021006661e-06 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Prominent occiput |
  HP:0009767 | 1.5670211959e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/Hypoplasia of the phalanges of the hand |
  HP:0000944 | 1.74155061016e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal metaphysis morphology |
  HP:0000773 | 2.21755710014e-06 | 0.666666666667 | IFT140 IFT122 WDR35 IFT43 | Short ribs |
  REAC:R-HSA-1852241 | 2.47115045635e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Organelle biogenesis and maintenance |
  HP:0009826 | 3.21680362051e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Limb undergrowth |
  HP:0008499 | 5.21207949413e-06 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | High hypermetropia |
  HP:0006482 | 5.90761647521e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal dental morphology |
  REAC:R-HSA-5610787 | 6.85992153937e-06 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Hedgehog 'off' state |
  HP:0009381 | 9.25651290097e-06 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Short finger |
  HP:0002983 | 9.52382922551e-06 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Micromelia |
  HP:0000772 | 1.11183549237e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal rib morphology |
  GO:0031503 | 1.258414027e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | protein-containing complex localization |
  REAC:R-HSA-5358351 | 1.67659998e-05 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Signaling by Hedgehog |
  HP:0006265 | 1.76739828051e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/Hypoplasia of fingers |
  GO:0010970 | 1.93005700328e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | transport along microtubule |
  HP:0011217 | 2.1709105889e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal shape of the occiput |
  HP:0009882 | 2.26206838432e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Short distal phalanx of finger |
  HP:0008070 | 2.35393522854e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Sparse hair |
  HP:0012294 | 2.35606190872e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal occipital bone morphology |
  HP:0011329 | 2.42767191814e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of cranial sutures |
  HP:0001156 | 2.50324136667e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Brachydactyly |
  HP:0001547 | 2.66001423518e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal rib cage morphology |
  HP:0009835 | 2.76156062683e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Aplasia/Hypoplasia of the distal phalanges of the hand |
  HP:0006712 | 3.21716924889e-05 | 0.666666666667 | IFT140 IFT122 WDR35 IFT43 | Aplasia/Hypoplasia of the ribs |
  HP:0004442 | 3.36277715305e-05 | 0.5 | IFT43 WDR19 IFT122 | Sagittal craniosynostosis |
  GO:0005929 | 3.40829569636e-05 | 1.0 | WDR19 IFT122 IFT43 IFT140 IFTAP WDR35 | cilium |
  GO:0099111 | 3.50374175094e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | microtubule-based transport |
  HP:0000083 | 3.51531007428e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Renal insufficiency |
  HP:0004209 | 3.66837991217e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Clinodactyly of the 5th finger |
  HP:0009179 | 3.72056880074e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Deviation of the 5th finger |
  HP:0002007 | 3.82672469355e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Frontal bossing |
  HP:0000687 | 3.86317345518e-05 | 0.666666666667 | IFT140 IFT122 WDR35 IFT43 | Widely spaced teeth |
  HP:0001159 | 3.8807016949e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Syndactyly |
  HP:0000968 | 3.92263544242e-05 | 0.5 | IFT43 IFT122 WDR35 | Ectodermal dysplasia |
  HP:0011218 | 3.99047900799e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal shape of the frontal region |
  HP:0430000 | 4.04628948337e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal frontal bone morphology |
  HP:0000973 | 4.29464917268e-05 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Cutis laxa |
  HP:0003774 | 4.29464917268e-05 | 0.666666666667 | IFT140 IFT122 WDR19 IFT43 | Stage 5 chronic kidney disease |
  HP:0001407 | 5.22168897407e-05 | 0.5 | IFT140 WDR19 IFT122 | Hepatic cysts |
  HP:0040019 | 5.30000762825e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Finger clinodactyly |
  HP:0000232 | 5.62183067184e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Everted lower lip vermilion |
  HP:0000293 | 5.80703630675e-05 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Full cheeks |
  HP:0001395 | 5.99676998675e-05 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Hepatic fibrosis |
  HP:0100259 | 5.99676998675e-05 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Postaxial polydactyly |
  HP:0000601 | 5.99676998675e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Hypotelorism |
  HP:0000766 | 6.26877314152e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal sternum morphology |
  HP:0000235 | 6.26877314152e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the fontanelles or cranial sutures |
  GO:0030705 | 6.51851913963e-05 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | cytoskeleton-dependent intracellular transport |
  HP:0008388 | 8.90924557824e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal toenail morphology |
  HP:0009832 | 9.17027073507e-05 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal distal phalanx morphology of finger |
  HP:0004207 | 0.000101662063112 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal 5th finger morphology |
  GO:0061512 | 0.000106291409046 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | protein localization to cilium |
  HP:0005927 | 0.000117817736994 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/hypoplasia involving bones of the hand |
  HP:0004097 | 0.000120475158955 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Deviation of finger |
  HP:0012472 | 0.00013813645411 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Eclabion |
  HP:0004349 | 0.000138937389081 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Reduced bone mineral density |
  HP:0009484 | 0.00015299090284 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Deviation of the hand or of fingers of the hand |
  HP:0006711 | 0.000153040914143 | 0.666666666667 | IFT140 IFT122 WDR35 IFT43 | Aplasia/Hypoplasia involving bones of the thorax |
  HP:0008067 | 0.000156947710561 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Abnormally lax or hyperextensible skin |
  HP:0006496 | 0.000164686603855 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/hypoplasia involving bones of the upper limbs |
  HP:0030084 | 0.000164686603855 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Clinodactyly |
  HP:0000090 | 0.000176135758605 | 0.5 | IFT140 WDR19 IFT43 | Nephronophthisis |
  HP:0001231 | 0.000177611776856 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal fingernail morphology |
  HP:0012622 | 0.000181977153209 | 0.666666666667 | IFT140 IFT122 WDR19 IFT43 | Chronic kidney disease |
  HP:0030799 | 0.00022859990461 | 0.5 | IFT140 IFT122 IFT43 | Scaphocephaly |
  HP:0006706 | 0.00022859990461 | 0.5 | IFT140 WDR19 IFT122 | Cystic liver disease |
  HP:0011927 | 0.000234335086831 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Short digit |
  HP:0004348 | 0.000253142887328 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of bone mineral density |
  HP:0002612 | 0.000268794104831 | 0.5 | IFT140 WDR19 WDR35 | Congenital hepatic fibrosis |
  HP:0000682 | 0.000269185172277 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal dental enamel morphology |
  HP:0000286 | 0.000286256639547 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Epicanthus |
  HP:0006101 | 0.00028733406656 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Finger syndactyly |
  HP:3000050 | 0.00036179605176 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal odontoid tissue morphology |
  HP:0045060 | 0.00039284272989 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/hypoplasia involving bones of the extremities |
  HP:0000668 | 0.000400032634721 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Hypodontia |
  HP:0005918 | 0.000432176588807 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal finger phalanx morphology |
  HP:0010647 | 0.000467390235865 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Abnormal elasticity of skin |
  HP:0012211 | 0.000474588206171 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal renal physiology |
  HP:0000178 | 0.000504080307199 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal lower lip morphology |
  HP:0011849 | 0.000542134971941 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal bone ossification |
  HP:0009815 | 0.000573995109675 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/hypoplasia of the extremities |
  HP:0004426 | 0.000605208682095 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormal cheek morphology |
  GO:0007018 | 0.000624476368572 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | microtubule-based movement |
  GO:0060271 | 0.000659970192201 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | cilium assembly |
  HP:0010442 | 0.000661105912226 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Polydactyly |
  HP:0000540 | 0.000672732345354 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Hypermetropia |
  HP:0100957 | 0.000727842944018 | 0.5 | IFT140 WDR19 IFT43 | Abnormal renal medulla morphology |
  HP:0011314 | 0.000727873953521 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal long bone morphology |
  HP:0006494 | 0.000771326645447 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Aplasia/Hypoplasia involving bones of the feet |
  GO:0044782 | 0.000939927808533 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | cilium organization |
  HP:0003330 | 0.000961121315124 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal bone structure |
  HP:0000939 | 0.000984794049706 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Osteoporosis |
  HP:0000940 | 0.00131506983485 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal diaphysis morphology |
  HP:0000767 | 0.00139398016067 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Pectus excavatum |
  HP:0011362 | 0.00145274392888 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal hair quantity |
  HP:0012440 | 0.00146741733922 | 0.5 | IFT140 WDR19 WDR35 | Abnormal biliary tract morphology |
  HP:0410042 | 0.00149218749136 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal liver morphology |
  HP:0002213 | 0.00160231496954 | 0.5 | IFT43 IFT122 WDR35 | Fine hair |
  HP:0006644 | 0.00161951205762 | 0.333333333333 | WDR35 WDR19 | Thoracic dysplasia |
  HP:0000765 | 0.00183941883667 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal thorax morphology |
  HP:0011061 | 0.00204945939855 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormality of dental structure |
  HP:0009804 | 0.00224410228317 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Tooth agenesis |
  HP:0001080 | 0.00240122360395 | 0.5 | IFT140 WDR19 WDR35 | Biliary tract abnormality |
  HP:0001162 | 0.00249319307056 | 0.5 | IFT140 WDR19 WDR35 | Postaxial hand polydactyly |
  HP:0006493 | 0.00251421996371 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Aplasia/hypoplasia involving bones of the lower limbs |
  HP:0004297 | 0.00267436793474 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormality of the biliary system |
  HP:0000164 | 0.00267809056162 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the dentition |
  HP:0002683 | 0.00275841306414 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal calvaria morphology |
  HP:0001105 | 0.00288444095262 | 0.5 | IFT140 WDR19 IFT43 | Retinal atrophy |
  HP:0006483 | 0.00339206501528 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal number of teeth |
  HP:0005922 | 0.00383825241604 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal hand morphology |
  HP:0000692 | 0.00384317259801 | 0.666666666667 | IFT140 IFT122 WDR35 IFT43 | Tooth malposition |
  HP:0000639 | 0.00394511883564 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Nystagmus |
  WP:WP4352 | 0.00400681842466 | 0.5 | IFT140 IFT122 IFT43 | Ciliary landscape |
  HP:0012547 | 0.00425698750482 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal involuntary eye movements |
  HP:0011277 | 0.00434960001953 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the urinary system physiology |
  HP:0001392 | 0.00442010530108 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the liver |
  GO:0120031 | 0.00450571144333 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | plasma membrane bounded cell projection assembly |
  HP:0000545 | 0.0046263330141 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Myopia |
  HP:0100886 | 0.00496538568106 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of globe location |
  HP:0007843 | 0.00500109820736 | 0.5 | IFT140 WDR19 IFT43 | Attenuation of retinal blood vessels |
  GO:0030031 | 0.00509483152423 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | cell projection assembly |
  HP:0012210 | 0.00517642268402 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal renal morphology |
  HP:0040070 | 0.00530098811513 | 0.666666666667 | IFT140 IFT122 WDR19 IFT43 | Abnormal upper limb bone morphology |
  HP:0001799 | 0.00593279372985 | 0.333333333333 | IFT43 IFT122 | Short nail |
  HP:0030151 | 0.00593279372985 | 0.333333333333 | IFT140 WDR35 | Cholangitis |
  HP:0000463 | 0.00680101690504 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Anteverted nares |
  HP:0002088 | 0.00686160531048 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal lung morphology |
  HP:0000290 | 0.00748705795004 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the forehead |
  HP:0004299 | 0.00776768683012 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Hernia of the abdominal wall |
  HP:0005288 | 0.0078404361426 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal nostril morphology |
  HP:0001597 | 0.0079136910806 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormality of the nail |
  HP:0010866 | 0.00798745393246 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abdominal wall defect |
  HP:0009115 | 0.00811857195519 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Aplasia/hypoplasia involving the skeleton |
  HP:0001167 | 0.00819556560378 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal finger morphology |
  HP:0001773 | 0.00857286967155 | 0.5 | IFT140 WDR19 WDR35 | Short foot |
  HP:0000159 | 0.00895634608406 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal lip morphology |
  HP:0000431 | 0.00923862134853 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Wide nasal bridge |
  HP:0004298 | 0.0107218211673 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormality of the abdominal wall |
  HP:0006703 | 0.0113637882169 | 0.5 | IFT140 WDR19 WDR35 | Aplasia/Hypoplasia of the lungs |
  HP:0002012 | 0.0113787764877 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the abdominal organs |
  HP:0001595 | 0.0120457334662 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal hair morphology |
  HP:0001382 | 0.0123751293622 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Joint hypermobility |
  HP:0000506 | 0.0138111776458 | 0.5 | IFT43 IFT122 WDR35 | Telecanthus |
  HP:0000492 | 0.0145979030629 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal eyelid morphology |
  HP:0000429 | 0.0146705398092 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormal morphology of the nasal alae |
  HP:0100790 | 0.0149045236961 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Hernia |
  HP:0004322 | 0.0155378546416 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Short stature |
  HP:0012252 | 0.0159270158081 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal respiratory system morphology |
  GO:0120025 | 0.0160788696948 | 1.0 | WDR19 IFT122 IFT43 IFT140 IFTAP WDR35 | plasma membrane bounded cell projection |
  HP:0000077 | 0.0163907734884 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the kidney |
  GO:0042995 | 0.0170600837211 | 1.0 | WDR19 IFT122 IFT43 IFT140 IFTAP WDR35 | cell projection |
  HP:0002205 | 0.0175320772209 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Recurrent respiratory infections |
  HP:0010935 | 0.0182080116735 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the upper urinary tract |
  HP:0001161 | 0.0182726158894 | 0.5 | IFT140 WDR19 WDR35 | Hand polydactyly |
  HP:0005105 | 0.0185751109679 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal nasal morphology |
  HP:0002652 | 0.0186233915395 | 0.5 | IFT140 WDR19 WDR35 | Skeletal dysplasia |
  HP:0000319 | 0.0186233915395 | 0.5 | IFT140 WDR19 WDR35 | Smooth philtrum |
  HP:0002644 | 0.0197536366037 | 0.666666666667 | IFT140 WDR19 WDR35 IFT43 | Abnormal pelvic girdle bone morphology |
  HP:0011138 | 0.0204198186076 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal skin adnexa morphology |
  HP:0000309 | 0.0209395955205 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormal midface morphology |
  HP:0002240 | 0.0212441588114 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Hepatomegaly |
  HP:0010719 | 0.0223788473695 | 0.5 | IFT43 IFT122 WDR35 | Abnormality of hair texture |
  HP:0001970 | 0.0226111656051 | 0.333333333333 | IFT122 WDR19 | Tubulointerstitial nephritis |
  HP:0009836 | 0.0226111656051 | 0.333333333333 | IFT122 WDR19 | Broad distal phalanx of finger |
  HP:0003549 | 0.0226657898986 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of connective tissue |
  HP:0011297 | 0.0228396399634 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal digit morphology |
  HP:0001760 | 0.0229269607293 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal foot morphology |
  HP:0000002 | 0.0229269607293 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of body height |
  HP:0000662 | 0.0261590153267 | 0.5 | IFT140 WDR19 IFT43 | Nyctalopia |
  HP:0030669 | 0.0286721248803 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal ocular adnexa morphology |
  HP:0001155 | 0.0291980155437 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the hand |
  HP:0000539 | 0.0297854763042 | 0.666666666667 | IFT43 IFT122 WDR19 WDR35 | Abnormality of refraction |
  HP:0032039 | 0.0302727333936 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the ocular adnexa |
  HP:0001780 | 0.0326351056455 | 0.666666666667 | IFT140 IFT122 WDR19 IFT43 | Abnormal toe morphology |
  HP:0000315 | 0.032863784458 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the orbital region |
  HP:0003271 | 0.0354575661861 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Visceromegaly |
  HP:4000059 | 0.0365652768554 | 0.5 | IFT140 WDR19 WDR35 | Abnormal lung development |
  HP:0009997 | 0.0399718389151 | 0.5 | IFT140 WDR19 WDR35 | Duplication of phalanx of hand |
  HP:0009142 | 0.0405591774535 | 0.5 | IFT140 WDR19 WDR35 | Duplication of bones involving the upper extremities |
  HP:0004275 | 0.0405591774535 | 0.5 | IFT140 WDR19 WDR35 | Duplication of hand bones |
  HP:0011947 | 0.0408888963229 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Respiratory tract infection |
  HP:0000366 | 0.0412870242376 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the nose |
  HP:0040069 | 0.0418928749121 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormal lower limb bone morphology |
  HP:0002817 | 0.0437114869583 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of the upper limb |
  HP:0040068 | 0.0445935923605 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of limb bone |
  HP:0002813 | 0.0445935923605 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormal limb bone morphology |
  HP:0001770 | 0.0454639361427 | 0.5 | IFT140 WDR19 IFT43 | Toe syndactyly |
  HP:0001737 | 0.0467604957305 | 0.333333333333 | IFT140 WDR19 | Pancreatic cysts |
  HP:0008046 | 0.0480563748242 | 0.5 | IFT140 WDR19 IFT43 | Abnormal retinal vascular morphology |
  HP:0000496 | 0.0495393048868 | 0.833333333333 | IFT140 IFT122 WDR19 WDR35 IFT43 | Abnormality of eye movement |
  HP:0001438 | 0.0497272491045 | 0.666666666667 | IFT140 IFT122 WDR19 WDR35 | Abnormal abdomen morphology |
Edges
Protein 1 | Protein 2 | Score | ProteomeHD | Evidence |
---|---|---|---|---|
 IFT43 |  WDR35 | 1.0 | 0.184           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT43 |  WDR19 | 1.0 | 0.154           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT140 |  IFT43 | 1.0 | 0.192           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT43 |  IFT122 | 1.0 | 0.224           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 WDR35 |  IFTAP | 0.999 |            | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT122 |  WDR19 | 0.999 | 0.188           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     boldt_WMM     |
 IFT43 |  IFTAP | 0.999 |            | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT140 |  IFT122 | 0.999 | 0.24           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     boldt_WMM     |
 IFT122 |  IFTAP | 0.999 |            | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 IFT140 |  IFTAP | 0.999 |            | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 WDR35 |  IFT122 | 0.998 | 0.18           | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     boldt_WMM     |
 WDR19 |  IFTAP | 0.998 |            | bioplex3_HEK293     bioplex ()     bioplex_WMM     bioplex3_WMM     boldt     bioplex3_HCT116     boldt_WMM     |
 WDR35 |  WDR19 | 0.998 | 0.208           | bioplex_WMM     bioplex3_WMM     boldt     boldt_WMM     WMM_only     |
 IFT140 |  WDR35 | 0.997 | 0.206           | bioplex_WMM     bioplex3_WMM     boldt     fraction     boldt_WMM     |
 IFT140 |  WDR19 | 0.994 | 0.262           | bioplex_WMM     bioplex3_WMM     boldt     fraction     boldt_WMM     |
Related Complexes
Genename | Complexes |
---|---|
IFT140 | huMAP3_03435.1 huMAP3_12868.1 |
IFT43 | huMAP3_03435.1 huMAP3_05176.1 huMAP3_12868.1 |
WDR35 | huMAP3_03435.1 huMAP3_12868.1 |
IFT122 | huMAP3_03435.1 huMAP3_12868.1 |
WDR19 | huMAP3_03435.1 huMAP3_12868.1 |
IFTAP | huMAP3_03435.1 huMAP3_12868.1 |