hu.MAP 3.0: Complex View
Human Protein Complex Map
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Complex: huMAP3_09871.1
Complex Portal: CPX-20290
Confidence: Moderate High  
ProteinsGenename | Protein Name | Uniprot Annotation Score | Links |
---|---|---|---|
CLEC4G | C-type lectin domain family 4 member G (Liver and lymph node sinusoidal endothelial cell C-type lectin) (LSECtin) | 5 | UniProt   NCBI |
AP4S1 | AP-4 complex subunit sigma-1 (AP-4 adaptor complex subunit sigma-1) (Adaptor-related protein complex 4 subunit sigma-1) (Sigma-1 subunit of AP-4) (Sigma-4-adaptin) (Sigma4-adaptin) | 5 | UniProt   NCBI |
TEPSIN | AP-4 complex accessory subunit Tepsin (ENTH domain-containing protein 2) (Epsin for AP-4) (Tetra-epsin) | 5 | UniProt   NCBI |
AP4M1 | AP-4 complex subunit mu-1 (AP-4 adaptor complex mu subunit) (Adaptor-related protein complex 4 subunit mu-1) (Mu subunit of AP-4) (Mu-adaptin-related protein 2) (mu-ARP2) (Mu4-adaptin) (mu4) | 5 | UniProt   NCBI |
DISC1 | Disrupted in schizophrenia 1 protein | 5 | UniProt   NCBI |
AP4E1 | AP-4 complex subunit epsilon-1 (AP-4 adaptor complex subunit epsilon) (Adaptor-related protein complex 4 subunit epsilon-1) (Epsilon subunit of AP-4) (Epsilon-adaptin) | 5 | UniProt   NCBI |
AP4B1 | AP-4 complex subunit beta-1 (AP-4 adaptor complex subunit beta) (Adaptor-related protein complex 4 subunit beta-1) (Beta subunit of AP-4) (Beta4-adaptin) | 5 | UniProt   NCBI |
Enrichments
Term ID | Corrected Pval | Fraction Complex Coverage | Proteins | Term Name |
---|---|---|---|---|
  CORUM:67 | 1.92263483365e-12 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | AP4 adaptor complex |
  GO:0030124 | 9.2094208532e-10 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | AP-4 adaptor complex |
  HP:5200020 | 3.27469978519e-09 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal interest in others |
  HP:0100962 | 3.27469978519e-09 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Shyness |
  HP:0008807 | 7.54279269726e-08 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Acetabular dysplasia |
  HP:0002464 | 9.31603571786e-08 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Spastic dysarthria |
  HP:0010803 | 1.13843939746e-07 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Everted upper lip vermilion |
  REAC:R-HSA-432720 | 1.4537101986e-07 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Lysosome Vesicle Biogenesis |
  HP:0007020 | 3.18339843159e-07 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Progressive spastic paraplegia |
  HP:0002816 | 6.3569022244e-07 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Genu recurvatum |
  HP:0002761 | 1.02533089038e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Generalized joint hypermobility |
  HP:0025502 | 1.02533089038e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Overweight |
  HP:0010500 | 1.14576950689e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Hyperextensibility of the knee |
  HP:0000297 | 1.9140162808e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Facial hypotonia |
  REAC:R-HSA-199992 | 3.23754553505e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | trans-Golgi Network Vesicle Budding |
  KEGG:04142 | 8.55799606515e-06 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Lysosome |
  GO:0032588 | 8.70757470934e-06 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 TEPSIN | trans-Golgi network membrane |
  GO:0031904 | 1.37183898061e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | endosome lumen |
  HP:0003170 | 1.97903117197e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal acetabulum morphology |
  HP:0034670 | 2.08712710555e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal knee physiology |
  GO:0030119 | 4.7975405982e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | AP-type membrane coat adaptor complex |
  HP:0002307 | 5.32614804607e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Drooling |
  HP:0000646 | 5.78468462937e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Amblyopia |
  HP:0001258 | 6.52705278452e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Spastic paraplegia |
  HP:0003781 | 7.33846660766e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Excessive salivation |
  HP:0002515 | 7.91979887457e-05 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Waddling gait |
  HP:0002518 | 0.000163150863658 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal periventricular white matter morphology |
  HP:0010550 | 0.000163150863658 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Paraplegia |
  HP:0012433 | 0.000240770135857 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal social behavior |
  HP:0000341 | 0.00032558864022 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Narrow forehead |
  HP:0012472 | 0.000352162394999 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Eclabion |
  HP:0100755 | 0.000522210892215 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of salivation |
  HP:0002465 | 0.000534555922747 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Poor speech |
  HP:0000414 | 0.000534555922747 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Bulbous nose |
  GO:0005802 | 0.000706434838609 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 TEPSIN | trans-Golgi network |
  HP:0010551 | 0.00083031577872 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Paraplegia/paraparesis |
  HP:0000154 | 0.000865451784044 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Wide mouth |
  HP:0002061 | 0.00101719310257 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Lower limb spasticity |
  HP:0000280 | 0.00114339230548 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Coarse facial features |
  HP:0002352 | 0.00121069743747 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Leukoencephalopathy |
  GO:0098791 | 0.00158704183469 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 TEPSIN | Golgi apparatus subcompartment |
  HP:0000322 | 0.0016494906913 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Short philtrum |
  GO:0048475 | 0.00202210317171 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | coated membrane |
  GO:0030117 | 0.00202210317171 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | membrane coat |
  HP:0000733 | 0.00205761005813 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal repetitive mannerisms |
  HP:0031432 | 0.00205761005813 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Restricted or repetitive behaviors or interests |
  HP:0031828 | 0.00261704338105 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal superficial reflex |
  HP:0003487 | 0.00261704338105 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Babinski sign |
  HP:0002355 | 0.00278364235165 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Difficulty walking |
  HP:0007370 | 0.00351193913333 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Aplasia/Hypoplasia of the corpus callosum |
  HP:0031815 | 0.00368511957341 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal oral physiology |
  HP:0000301 | 0.00368511957341 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of facial musculature |
  HP:0002538 | 0.00388394682689 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal cerebral cortex morphology |
  HP:0002120 | 0.00524994434086 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Cerebral cortical atrophy |
  HP:0001763 | 0.00545788958387 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Pes planus |
  HP:0033725 | 0.00588607227615 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Thin corpus callosum |
  HP:0010864 | 0.00635143461582 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Intellectual disability, severe |
  HP:0001384 | 0.00675412452899 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal hip joint morphology |
  HP:0000436 | 0.00726204381131 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal nasal tip morphology |
  HP:0034353 | 0.00855715073648 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Appendicular spasticity |
  HP:0001273 | 0.00857848314082 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal corpus callosum morphology |
  HP:0002815 | 0.00895676768606 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of the knee |
  HP:0001762 | 0.00905879972047 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Talipes equinovarus |
  HP:0011337 | 0.0112864591849 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of mouth size |
  HP:0001317 | 0.0129343410886 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal cerebellum morphology |
  HP:0007256 | 0.0129372325986 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal pyramidal sign |
  HP:0011282 | 0.0132236264343 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal hindbrain morphology |
  HP:0011283 | 0.0132236264343 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal metencephalon morphology |
  HP:0001272 | 0.0136175114425 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Cerebellar atrophy |
  REAC:R-HSA-199991 | 0.0144304646027 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Membrane Trafficking |
  HP:0011339 | 0.014908406472 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of upper lip vermillion |
  HP:0004324 | 0.0159734802208 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Increased body weight |
  HP:0001883 | 0.0162878804703 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Talipes |
  HP:0005656 | 0.016930414323 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Positional foot deformity |
  HP:0002079 | 0.0174244995856 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Hypoplasia of the corpus callosum |
  REAC:R-HSA-5653656 | 0.0178473234243 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Vesicle-mediated transport |
  HP:0002500 | 0.0196649485966 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal cerebral white matter morphology |
  HP:0004302 | 0.0196899667773 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Functional motor deficit |
  HP:0011799 | 0.0213813331773 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormality of facial soft tissue |
  HP:0010549 | 0.0221665967647 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Weakness due to upper motor neuron dysfunction |
  HP:0001332 | 0.0255228404391 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Dystonia |
  HP:0100021 | 0.0281302035428 | 0.428571428571 | AP4S1 AP4M1 AP4E1 | Cerebral palsy |
  HP:0010993 | 0.0284983301401 | 0.714285714286 | AP4S1 AP4B1 AP4M1 AP4E1 DISC1 | Abnormal cerebral subcortex morphology |
  HP:0001382 | 0.030987905771 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Joint hypermobility |
  HP:0003272 | 0.0317596619846 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal hip bone morphology |
  HP:0007663 | 0.0341603212271 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Reduced visual acuity |
  HP:0001319 | 0.0405415169637 | 0.428571428571 | AP4E1 AP4M1 AP4B1 | Neonatal hypotonia |
  HP:0001260 | 0.0434648219475 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Dysarthria |
  HP:0002644 | 0.0492980006882 | 0.571428571429 | AP4S1 AP4B1 AP4M1 AP4E1 | Abnormal pelvic girdle bone morphology |
  CORUM:7235 | 0.0499958217778 | 0.142857142857 | DISC1 | DISC1-DRD2 complex |
Edges
Protein 1 | Protein 2 | Score | ProteomeHD | Interface Overlap | Evidence |
---|---|---|---|---|---|
 AP4E1 |  TEPSIN | 1.0 | 0.138           |          | hein_WMM     bioplex3_HEK293     bioplex3_WMM     hein ()     bioplex3_HCT116     |
 AP4S1 |  AP4B1 | 1.0 | 0.172           |
structurally_consistent (dimer)        
|
hein_WMM     bioplex3_HEK293     bioplex3_WMM     youn_WMM     hein ()     bioplex3_HCT116     gupta_WMM     |
 AP4E1 |  AP4B1 | 1.0 | 0.284           |
mutually_exclusive (Q9Y587)        
|
hein_WMM     bioplex3_HEK293     bioplex3_WMM     youn_WMM     hein ()     bioplex3_HCT116     gupta_WMM     |
 AP4M1 |  AP4E1 | 1.0 | 0.17           |
mutually_exclusive (Q9Y587)        
|
hein_WMM     bioplex3_HEK293     bioplex_WMM     bioplex3_WMM     youn_WMM     hein ()     gupta_WMM     |
 AP4M1 |  TEPSIN | 1.0 | 0.078           |          | hein_WMM     bioplex3_HEK293     bioplex3_WMM     hein ()     bioplex3_HCT116     |
 AP4M1 |  AP4B1 | 0.999 | 0.18           |
structurally_consistent (dimer)        
|
hein_WMM     bioplex3_HEK293     bioplex3_WMM     youn_WMM     bioplex3_HCT116     gupta_WMM     WMM_only     |
 AP4S1 |  AP4M1 | 0.999 | 0.112           |
mutually_exclusive (Q9Y6B7)        
structurally_consistent (dimer)         |
hein_WMM     bioplex_WMM     bioplex3_WMM     hein ()     gupta_WMM     |
 AP4S1 |  AP4E1 | 0.999 | 0.166342857143           |
structurally_consistent (dimer)        
|
hein_WMM     bioplex3_HEK293     bioplex_WMM     bioplex3_WMM     youn_WMM     hein ()     gupta_WMM     |
 AP4B1 |  TEPSIN | 0.998 | 0.172           |
mutually_exclusive (Q9Y587)        
|
hein_WMM     bioplex3_HEK293     bioplex3_WMM     bioplex3_HCT116     WMM_only     |
 AP4S1 |  TEPSIN | 0.998 | 0.126           |
structurally_consistent (dimer)        
|
hein_WMM     bioplex3_HEK293     bioplex3_WMM     bioplex3_HCT116     WMM_only     |
 AP4S1 |  DISC1 | 0.994 | 0.066           |
structurally_consistent (O00189)        
|
bioplex3_HEK293     bioplex3_WMM     bioplex3_HCT116     WMM_only     |
 AP4E1 |  DISC1 | 0.993 | 0.154           |          | bioplex3_HEK293     bioplex3_WMM     bioplex3_HCT116     WMM_only     |
 CLEC4G |  TEPSIN | 0.986 |            |          | bioplex3_HEK293     bioplex3_WMM     WMM_only     |
 AP4B1 |  DISC1 | 0.978 | 0.134           |          | bioplex3_HEK293     bioplex3_WMM     bioplex3_HCT116     WMM_only     |
 AP4M1 |  DISC1 | 0.925 | 0.122           |
structurally_consistent (dimer)        
|
bioplex3_HEK293     bioplex3_WMM     WMM_only     |
 AP4B1 |  CLEC4G | 0.415 |            |          | bioplex3_WMM     WMM_only     |
 AP4M1 |  CLEC4G | 0.278 |            |          | bioplex3_WMM     WMM_only     |
 AP4E1 |  CLEC4G | 0.278 |            |          | bioplex3_WMM     WMM_only     |
 AP4S1 |  CLEC4G | 0.274 |            |          | bioplex3_WMM     WMM_only     |
Related Complexes