hu.MAP 3.0: Complex View

Human Protein Complex Map

Complex: huMAP3_12868.1

Confidence: Medium

Genename	Protein Name	Uniprot Annotation Score	Links
IFT140	Intraflagellar transport protein 140 homolog (WD and tetratricopeptide repeats protein 2)	5	UniProt NCBI
LYSMD1	LysM and putative peptidoglycan-binding domain-containing protein 1	4	UniProt NCBI
UBA1	Ubiquitin-like modifier-activating enzyme 1 (EC 6.2.1.45) (Protein A1S9) (Ubiquitin-activating enzyme E1)	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
TUB	Tubby protein homolog	5	UniProt NCBI
IFT122	Intraflagellar transport protein 122 homolog (WD repeat-containing protein 10) (WD repeat-containing protein 140)	5	UniProt NCBI
SCO1	Protein SCO1 homolog, mitochondrial	5	UniProt NCBI
WDR19	WD repeat-containing protein 19 (Intraflagellar transport 144 homolog)	5	UniProt NCBI
ZKSCAN5	Zinc finger protein with KRAB and SCAN domains 5 (Zinc finger protein 95 homolog) (Zfp-95)	4	UniProt NCBI
TULP1	Tubby-related protein 1 (Tubby-like protein 1)	5	UniProt NCBI
TTC21B	Tetratricopeptide repeat protein 21B (TPR repeat protein 21B) (Intraflagellar transport 139 homolog)	5	UniProt NCBI
ANKRD54	Ankyrin repeat domain-containing protein 54 (Lyn-interacting ankyrin repeat protein)	3	UniProt NCBI
IFTAP	Intraflagellar transport-associated protein (Protein HEPIS)	3	UniProt NCBI
SMYD5	Histone-lysine N-trimethyltransferase SMYD5 (EC 2.1.1.372) (Protein NN8-4AG) (Retinoic acid-induced protein 15) (SET and MYND domain-containing protein 5) ([histone H4]-lysine20 N-trimethyltransferase SMYD5)	5	UniProt NCBI
TULP3	Tubby-related protein 3 (Tubby-like protein 3)	5	UniProt NCBI

Enrichments

Term ID	Corrected Pval	Fraction Complex Coverage	Proteins	Term Name
GO:0030991	1.85079984885e-14	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	intraciliary transport particle A
CORUM:6585	2.62526075648e-14	0.333333333333	TTC21B IFT140 WDR19 IFT122 WDR35	Intraflagellar transport complex A
GO:0061512	4.61166419464e-12	0.533333333333	TTC21B TULP3 TULP1 WDR19 TUB WDR35 IFT140 IFT122	protein localization to cilium
GO:0035721	3.16424989393e-11	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	intraciliary retrograde transport
WP:WP4803	9.44092746785e-11	0.533333333333	TTC21B IFT43 WDR35 TUB WDR19 TULP1 IFT140 IFT122	Ciliopathies
GO:0042073	3.02485340266e-10	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	intraciliary transport
WP:WP4536	3.35537998775e-10	0.466666666667	IFT43 TULP3 WDR35 WDR19 TTC21B IFT140 IFT122	Genes related to primary cilium development based on CRISPR
GO:0030990	1.85161938359e-09	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	intraciliary transport particle
REAC:R-HSA-5620924	1.94899182524e-09	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Intraflagellar transport
WP:WP4532	4.79047295891e-09	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Intraflagellar transport proteins binding to dynein
WP:WP5234	8.66463578774e-09	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Bardet Biedl syndrome
GO:0005929	6.62596384267e-08	0.666666666667	TTC21B IFT43 IFTAP WDR35 TUB WDR19 TULP3 TULP1 IFT140 IFT122	cilium
GO:0097542	1.47672361818e-07	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	ciliary tip
REAC:R-HSA-5610787	1.69249653805e-07	0.4	TULP3 WDR35 WDR19 IFT140 TTC21B IFT122	Hedgehog 'off' state
HP:0010306	3.87569483938e-07	0.333333333333	TTC21B IFT140 WDR19 IFT122 WDR35	Short thorax
REAC:R-HSA-5358351	6.48243574725e-07	0.4	TULP3 WDR35 WDR19 IFT140 TTC21B IFT122	Signaling by Hedgehog
HP:0000774	7.88661774334e-07	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Narrow chest
GO:0031503	8.59056257636e-07	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	protein-containing complex localization
GO:0010970	1.56395501957e-06	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	transport along microtubule
HP:0100957	1.8478861238e-06	0.333333333333	TTC21B IFT140 TULP3 WDR19 IFT43	Abnormal renal medulla morphology
HP:0005257	2.19190025924e-06	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Thoracic hypoplasia
HP:0008905	3.46225995941e-06	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Rhizomelia
GO:0099111	3.60089483813e-06	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	microtubule-based transport
REAC:R-HSA-5617833	5.87636122247e-06	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Cilium Assembly
HP:0001407	6.98715269064e-06	0.266666666667	TTC21B IFT140 IFT122 WDR19	Hepatic cysts
GO:0030705	8.56596026908e-06	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	cytoskeleton-dependent intracellular transport
HP:0002983	1.38394497849e-05	0.333333333333	TTC21B IFT140 WDR19 WDR35 IFT43	Micromelia
HP:0000944	2.47165565792e-05	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal metaphysis morphology
HP:0008873	2.96971816665e-05	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Disproportionate short-limb short stature
HP:0000090	3.6351691379e-05	0.266666666667	TTC21B IFT140 WDR19 IFT43	Nephronophthisis
GO:0120160	4.37346186898e-05	0.2	IFTAP TUB TULP3	intraciliary transport particle A binding
HP:0007843	4.73494129862e-05	0.333333333333	TULP1 IFT140 WDR19 TUB IFT43	Attenuation of retinal blood vessels
HP:0009826	5.11132822018e-05	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Limb undergrowth
HP:0006706	5.16756037585e-05	0.266666666667	TTC21B IFT140 IFT122 WDR19	Cystic liver disease
REAC:R-HSA-1852241	5.46193073928e-05	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Organelle biogenesis and maintenance
HP:0003498	8.28824189681e-05	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Disproportionate short stature
HP:0003774	9.04491962142e-05	0.333333333333	TTC21B IFT140 WDR19 IFT122 IFT43	Stage 5 chronic kidney disease
HP:0011071	9.62109054887e-05	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal permanent molar morphology
HP:0000679	9.62109054887e-05	0.266666666667	IFT43 WDR19 IFT122 WDR35	Taurodontia
HP:0011070	0.00011601701553	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal molar morphology
HP:0011077	0.000126989624977	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormality of molar
HP:0001395	0.000136938246516	0.333333333333	IFT140 WDR19 IFT122 TULP3 WDR35	Hepatic fibrosis
HP:0100259	0.000136938246516	0.333333333333	TTC21B IFT140 WDR19 WDR35 IFT43	Postaxial polydactyly
HP:0006479	0.000138718902694	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal dental pulp morphology
HP:0006486	0.000138718902694	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal dental root morphology
HP:0000269	0.000164582536196	0.266666666667	IFT43 WDR19 IFT122 WDR35	Prominent occiput
HP:0007703	0.00019414168186	0.4	IFT43 TULP1 WDR19 TUB TTC21B IFT140	Abnormality of retinal pigmentation
GO:0007018	0.000197728017861	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	microtubule-based movement
GO:0097731	0.000215823179568	0.333333333333	IFTAP TULP1 TULP3 IFT122 WDR19	9+0 non-motile cilium
HP:0000772	0.000220746387668	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal rib morphology
HP:0410042	0.000225869068025	0.533333333333	IFT43 TULP3 WDR35 WDR19 SCO1 TTC21B IFT140 IFT122	Abnormal liver morphology
HP:0000773	0.000284103610337	0.266666666667	IFT122 IFT140 WDR35 IFT43	Short ribs
GO:0044782	0.000347960435132	0.466666666667	IFT43 WDR35 TUB WDR19 TTC21B IFT140 IFT122	cilium organization
HP:0000691	0.000410582129362	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Microdontia
HP:0009803	0.000494744636089	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Short phalanx of finger
HP:0001363	0.000510009625948	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Craniosynostosis
HP:0012622	0.000541658577759	0.333333333333	TTC21B IFT140 WDR19 IFT122 IFT43	Chronic kidney disease
HP:0001156	0.000572318698163	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Brachydactyly
HP:0001547	0.000614515944976	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal rib cage morphology
HP:0008499	0.000663476346285	0.266666666667	IFT43 WDR19 IFT122 WDR35	High hypermetropia
HP:0000268	0.000724046407085	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Dolichocephaly
HP:0000662	0.000744666197971	0.333333333333	TULP1 IFT140 WDR19 TUB IFT43	Nyctalopia
GO:0097730	0.000797934456619	0.333333333333	IFTAP TULP1 TULP3 IFT122 WDR19	non-motile cilium
HP:0000083	0.000851511667566	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Renal insufficiency
HP:0001159	0.000955827342869	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Syndactyly
HP:0009767	0.00103036818808	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Aplasia/Hypoplasia of the phalanges of the hand
HP:0004442	0.00109639830438	0.2	IFT43 IFT122 WDR19	Sagittal craniosynostosis
HP:0001392	0.00120804643527	0.533333333333	IFT43 TULP3 WDR35 WDR19 SCO1 TTC21B IFT140 IFT122	Abnormality of the liver
HP:0000545	0.0012149870404	0.4	IFT43 TULP1 WDR19 TUB WDR35 IFT122	Myopia
HP:0001162	0.00126764773979	0.266666666667	TTC21B IFT140 WDR19 WDR35	Postaxial hand polydactyly
HP:0000968	0.00127834331529	0.2	IFT43 IFT122 WDR35	Ectodermal dysplasia
GO:0120025	0.0015138591657	0.666666666667	TTC21B IFT43 IFTAP WDR35 TUB WDR19 TULP3 TULP1 IFT140 IFT122	plasma membrane bounded cell projection
HP:0001105	0.00153901495334	0.266666666667	IFT140 WDR19 TUB IFT43	Retinal atrophy
GO:0042995	0.001664498933	0.666666666667	TTC21B IFT43 IFTAP WDR35 TUB WDR19 TULP3 TULP1 IFT140 IFT122	cell projection
HP:0000766	0.00167235691703	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal sternum morphology
HP:0007737	0.00168983362344	0.266666666667	TULP1 IFT140 TUB IFT43	Bone spicule pigmentation of the retina
HP:0008046	0.00203702217847	0.333333333333	TULP1 IFT140 WDR19 TUB IFT43	Abnormal retinal vascular morphology
HP:0010442	0.00265421893369	0.333333333333	TTC21B IFT140 WDR19 WDR35 IFT43	Polydactyly
HP:0000540	0.00271163932033	0.333333333333	TULP1 IFT43 WDR19 IFT122 WDR35	Hypermetropia
HP:0011217	0.0027241718837	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal shape of the occiput
HP:0009882	0.00283715894368	0.266666666667	IFT43 WDR19 IFT122 WDR35	Short distal phalanx of finger
HP:0004207	0.00293404743625	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal 5th finger morphology
HP:0012294	0.00295358855383	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal occipital bone morphology
HP:0006494	0.0032071480257	0.333333333333	TTC21B IFT140 WDR19 IFT122 WDR35	Aplasia/Hypoplasia involving bones of the feet
HP:0009835	0.00345508924633	0.266666666667	IFT43 WDR19 IFT122 WDR35	Aplasia/Hypoplasia of the distal phalanges of the hand
HP:0000546	0.00348029049205	0.333333333333	TULP1 IFT140 WDR19 TUB IFT43	Retinal degeneration
HP:0006482	0.00377145112069	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Abnormal dental morphology
HP:0006712	0.00401716707369	0.266666666667	IFT122 IFT140 WDR35 IFT43	Aplasia/Hypoplasia of the ribs
HP:0000687	0.00481190103995	0.266666666667	IFT122 IFT140 WDR35 IFT43	Widely spaced teeth
HP:0002012	0.0051296229563	0.533333333333	IFT43 TULP3 WDR35 WDR19 SCO1 TTC21B IFT140 IFT122	Abnormality of the abdominal organs
HP:0000973	0.00534141102818	0.266666666667	IFT140 WDR19 WDR35 IFT43	Cutis laxa
HP:0009381	0.00583931278594	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Short finger
HP:0001773	0.00652851933941	0.266666666667	TTC21B IFT140 WDR19 WDR35	Short foot
HP:0000232	0.00696446920409	0.266666666667	IFT43 WDR19 IFT122 WDR35	Everted lower lip vermilion
HP:0000293	0.00719034985144	0.266666666667	IFT140 WDR19 IFT122 WDR35	Full cheeks
HP:0030799	0.00739493145726	0.2	IFT140 IFT122 IFT43	Scaphocephaly
HP:0000601	0.00742160924832	0.266666666667	IFT43 WDR19 IFT122 WDR35	Hypotelorism
HP:0011927	0.00770942261108	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Short digit
HP:0000479	0.00774947503091	0.466666666667	IFT43 TULP1 WDR19 TUB TTC21B IFT140 IFT122	Abnormal retinal morphology
HP:0002612	0.00868713170593	0.2	IFT140 WDR19 WDR35	Congenital hepatic fibrosis
GO:0060271	0.00892718765068	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	cilium assembly
HP:0000556	0.00915441900189	0.333333333333	TULP1 IFT140 WDR19 TUB IFT122	Retinal dystrophy
GO:0033365	0.00915712934984	0.533333333333	TTC21B TULP3 TULP1 WDR19 TUB WDR35 IFT140 IFT122	protein localization to organelle
HP:0006703	0.00947525460656	0.266666666667	TTC21B IFT140 WDR19 WDR35	Aplasia/Hypoplasia of the lungs
HP:0000119	0.00991857352522	0.666666666667	TTC21B IFT43 TULP3 WDR35 TUB IFT122 TULP1 IFT140 WDR19 SCO1	Abnormality of the genitourinary system
HP:0006265	0.0109371126609	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Aplasia/Hypoplasia of fingers
HP:0008388	0.0109554160497	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal toenail morphology
HP:0002240	0.0112610916338	0.4	TULP3 WDR35 WDR19 IFT122 IFT140 SCO1	Hepatomegaly
HP:0009832	0.0112708127877	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal distal phalanx morphology of finger
HP:0006493	0.0135880830026	0.333333333333	TTC21B IFT140 WDR19 IFT122 WDR35	Aplasia/hypoplasia involving bones of the lower limbs
HP:0045060	0.0139657178751	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Aplasia/hypoplasia involving bones of the extremities
HP:0008047	0.0142165704763	0.333333333333	TULP1 IFT140 WDR19 TUB IFT43	Abnormality of the vasculature of the eye
HP:0008070	0.0144310537755	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Sparse hair
HP:0004297	0.0146480661571	0.333333333333	IFT140 WDR19 IFT122 TULP3 WDR35	Abnormality of the biliary system
HP:0011329	0.0148676289874	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Abnormality of cranial sutures
HP:0005918	0.0155805123112	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal finger phalanx morphology
HP:0000639	0.0157135800556	0.466666666667	IFT43 WDR35 TUB WDR19 TULP1 IFT140 IFT122	Nystagmus
HP:0006644	0.0163481858886	0.133333333333	WDR35 WDR19	Thoracic dysplasia
HP:0032948	0.0163481858886	0.133333333333	TULP3 WDR19	Renal interstitial fibrosis
HP:0012472	0.0168522425975	0.266666666667	IFT43 WDR19 IFT122 WDR35	Eclabion
HP:0012211	0.0173441574134	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal renal physiology
HP:0012547	0.0173795322389	0.466666666667	IFT43 WDR35 TUB WDR19 TULP1 IFT140 IFT122	Abnormal involuntary eye movements
HP:0001161	0.0177264239099	0.266666666667	TTC21B IFT140 WDR19 WDR35	Hand polydactyly
HP:0011277	0.0178817473083	0.466666666667	IFT43 WDR35 WDR19 SCO1 TTC21B IFT140 IFT122	Abnormality of the urinary system physiology
HP:0002652	0.018175843844	0.266666666667	TTC21B IFT140 WDR19 WDR35	Skeletal dysplasia
HP:0000539	0.0183725435659	0.4	IFT43 TULP1 WDR19 TUB WDR35 IFT122	Abnormality of refraction
HP:0006711	0.0186336136568	0.266666666667	IFT122 IFT140 WDR35 IFT43	Aplasia/Hypoplasia involving bones of the thorax
HP:0008067	0.0190998317058	0.266666666667	IFT140 WDR19 WDR35 IFT43	Abnormally lax or hyperextensible skin
HP:0000580	0.0195745968169	0.266666666667	TULP1 IFT140 TUB IFT43	Pigmentary retinopathy
HP:0009815	0.02155866366	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Aplasia/hypoplasia of the extremities
HP:0001231	0.0215611206796	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal fingernail morphology
HP:0004209	0.022140978532	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Clinodactyly of the 5th finger
HP:0009179	0.0224442795813	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Deviation of the 5th finger
HP:0012210	0.0225072613653	0.466666666667	IFT43 TULP3 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal renal morphology
HP:0002007	0.0230606303005	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Frontal bossing
HP:0032581	0.0233605712246	0.2	TULP3 IFT122 WDR19	Abnormal renal insterstitial morphology
HP:0003271	0.0236334149928	0.4	TULP3 WDR35 WDR19 IFT122 IFT140 SCO1	Visceromegaly
HP:0000007	0.0237771974468	0.666666666667	TTC21B IFT43 TULP3 WDR35 TUB IFT122 TULP1 IFT140 WDR19 SCO1	Autosomal recessive inheritance
HP:0011218	0.0240099001657	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Abnormal shape of the frontal region
HP:0430000	0.0243330218246	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Abnormal frontal bone morphology
HP:0011314	0.0282702311288	0.4	IFT43 WDR35 WDR19 TTC21B IFT140 IFT122	Abnormal long bone morphology
HP:0040019	0.0315419930105	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Finger clinodactyly
HP:0000682	0.0323876617037	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal dental enamel morphology
HP:0006101	0.0345199547462	0.266666666667	IFT43 WDR19 IFT122 WDR35	Finger syndactyly
HP:0000235	0.0370553619006	0.333333333333	IFT122 IFT140 WDR19 WDR35 IFT43	Abnormality of the fontanelles or cranial sutures
HP:0001830	0.037193117608	0.2	IFT140 WDR19 TTC21B	Postaxial foot polydactyly
HP:0001438	0.0384661626611	0.4	TULP3 WDR35 WDR19 IFT122 IFT140 SCO1	Abnormal abdomen morphology
HP:3000050	0.0432294948784	0.266666666667	IFT43 WDR19 IFT122 WDR35	Abnormal odontoid tissue morphology
HP:4000059	0.0440940896345	0.266666666667	TTC21B IFT140 WDR19 WDR35	Abnormal lung development
HP:0012440	0.0467938914103	0.2	IFT140 WDR19 WDR35	Abnormal biliary tract morphology
HP:0000668	0.0476799439421	0.266666666667	IFT43 WDR19 IFT122 WDR35	Hypodontia
HP:0009997	0.0495509857294	0.266666666667	TTC21B IFT140 WDR19 WDR35	Duplication of phalanx of hand
HP:0000543	0.0495509857294	0.266666666667	TULP1 IFT140 TUB IFT43	Optic disc pallor

Edges

Protein 1	Protein 2	Score	ProteomeHD
IFT43	WDR35	1.0	0.184
IFT43	WDR19	1.0	0.154
IFT140	IFT43	1.0	0.192
IFT43	IFT122	1.0	0.224
TTC21B	IFT43	1.0	0.166
WDR35	IFTAP	0.999
IFT122	WDR19	0.999	0.188
IFT43	IFTAP	0.999
IFT140	IFT122	0.999	0.24
IFT122	IFTAP	0.999
TTC21B	TULP3	0.999	0.174
WDR19	TULP3	0.999	0.157454545455
IFT140	IFTAP	0.999
WDR35	TULP3	0.999	0.212
WDR35	IFT122	0.998	0.18
ANKRD54	TULP3	0.998	0.106
IFT122	TULP3	0.998	0.179111111111
WDR19	IFTAP	0.998
WDR35	WDR19	0.998	0.208
IFT140	TULP3	0.998	0.126
TULP1	TULP3	0.997
IFT140	WDR35	0.997	0.206
IFT43	ZKSCAN5	0.995
IFT140	WDR19	0.994	0.262
LYSMD1	TULP3	0.994	0.092
IFT43	TULP3	0.983	0.16
TUB	TULP3	0.98
TTC21B	WDR35	0.931	0.324
TTC21B	WDR19	0.925	0.278
SMYD5	TUB	0.903
TTC21B	IFT122	0.902	0.286
IFTAP	ZKSCAN5	0.902
TTC21B	IFT140	0.899	0.232
TTC21B	ZKSCAN5	0.883
TTC21B	IFTAP	0.848
WDR35	ZKSCAN5	0.848
ANKRD54	TUB	0.848
WDR19	SCO1	0.846	0.0841827411168
TTC21B	SCO1	0.846	0.098
TTC21B	UBA1	0.846	0.094
WDR35	SCO1	0.811	0.142
WDR19	ZKSCAN5	0.696
IFT43	SCO1	0.678	0.028
ANKRD54	TTC21B	0.581	0.12
ANKRD54	WDR35	0.581	0.15
ANKRD54	WDR19	0.57	0.078
LYSMD1	TULP1	0.557
TTC21B	LYSMD1	0.543	0.146
WDR35	LYSMD1	0.543	0.138
WDR35	TULP1	0.543
TTC21B	TULP1	0.543
IFTAP	TULP3	0.502
LYSMD1	TUB	0.487
TUB	TULP1	0.487
WDR19	TULP1	0.35
WDR19	LYSMD1	0.35	0.118
ANKRD54	LYSMD1	0.35	0.104
ANKRD54	IFT43	0.346	0.118
ANKRD54	TULP1	0.305
IFT122	ZKSCAN5	0.262
IFT140	TUB	0.233
WDR19	TUB	0.213
IFT43	LYSMD1	0.2	0.261
IFT43	TULP1	0.2
TTC21B	TUB	0.172
IFT140	TULP1	0.164
WDR35	TUB	0.164
IFT140	LYSMD1	0.164	0.086
ANKRD54	IFT122	0.142	0.06
IFT122	SCO1	0.141	0.14
IFT122	TUB	0.141
IFT122	LYSMD1	0.138	0.104
IFT122	TULP1	0.138
ZKSCAN5	TULP3	0.131
ANKRD54	IFT140	0.122	0.092
IFT140	ZKSCAN5	0.116
ANKRD54	SCO1	0.093	0.018
IFT140	SCO1	0.059	0.118
IFT43	TUB	0.048
SCO1	TUB	0.029
SMYD5	SCO1	0.025	0.018
WDR35	UBA1	0.023	0.192
WDR19	UBA1	0.011	0.132
ANKRD54	UBA1	0.008	0.202
SCO1	UBA1	0.007	0.112
SCO1	TULP3	0.007	0.202
SMYD5	UBA1	0.007	0.108
IFTAP	UBA1	0.007
IFT140	UBA1	0.005	0.196
TUB	UBA1	0.005
IFT122	UBA1	0.002	0.2
IFT43	UBA1	0.002	0.112
TULP3	UBA1	0.001	0.142

Related Complexes

Genename	Complexes
IFT140	huMAP3_03435.1 huMAP3_12868.1
LYSMD1	huMAP3_04948.1 huMAP3_08110.1 huMAP3_11707.1 huMAP3_12868.1 huMAP3_14418.1
UBA1	huMAP3_11939.1 huMAP3_12868.1 huMAP3_14980.1 huMAP3_15101.1
IFT43	huMAP3_03435.1 huMAP3_05176.1 huMAP3_12868.1
WDR35	huMAP3_03435.1 huMAP3_12868.1
TUB	huMAP3_04948.1 huMAP3_08110.1 huMAP3_11707.1 huMAP3_11900.1 huMAP3_12868.1 huMAP3_14418.1 huMAP3_15139.1
IFT122	huMAP3_03435.1 huMAP3_12868.1
SCO1	huMAP3_04170.1 huMAP3_09908.1 huMAP3_12868.1
WDR19	huMAP3_03435.1 huMAP3_12868.1
ZKSCAN5	huMAP3_04361.1 huMAP3_05176.1 huMAP3_06984.1 huMAP3_08576.1 huMAP3_10438.1 huMAP3_12868.1 huMAP3_14807.1
TULP1	huMAP3_04948.1 huMAP3_08110.1 huMAP3_11707.1 huMAP3_12868.1 huMAP3_14418.1
TTC21B	huMAP3_03200.1 huMAP3_05604.1 huMAP3_05723.1 huMAP3_09727.1 huMAP3_10816.1 huMAP3_11939.1 huMAP3_12868.1 huMAP3_14980.1
ANKRD54	huMAP3_01274.1 huMAP3_05643.1 huMAP3_06731.1 huMAP3_10539.1 huMAP3_11707.1 huMAP3_12868.1 huMAP3_14418.1 huMAP3_14607.1 huMAP3_15139.1
IFTAP	huMAP3_03435.1 huMAP3_12868.1
SMYD5	huMAP3_02963.1 huMAP3_03143.1 huMAP3_05542.1 huMAP3_08350.1 huMAP3_10047.1 huMAP3_11707.1 huMAP3_11900.1 huMAP3_12868.1 huMAP3_14418.1 huMAP3_15139.1
TULP3	huMAP3_04948.1 huMAP3_08110.1 huMAP3_11707.1 huMAP3_12868.1 huMAP3_14418.1

hu.MAP 3.0: Complex View

Search for a protein

Complex: huMAP3_12868.1