MEGF10 and AP2M1

  • Data Source:
  • HPRD (two hybrid)

MEGF10

AP2M1

Description multiple EGF like domains 10 adaptor related protein complex 2 subunit mu 1
Image No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Alzheimer's disease (cognitive decline) ( 23535033)
  • Bone mineral content ( 31790847)
  • Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure ( 31586183)
  • Hearing loss in Charcot-Marie-Tooth disease 1A ( 30958311)
  • Initial pursuit acceleration ( 29064472)
  • Response to antipsychotic treatment in schizophrenia ( 29503163)
Interacting Genes 23 interacting genes: AARS2 ALMS1 AP2M1 ARHGAP32 BAHD1 CADPS2 CEP57 CUL7 DHX16 GRB10 GULP1 HDAC4 ITSN2 MCF2L2 RANBP10 SART3 SCAPER SHTN1 SNRNP200 TAOK2 TMEM132A VWA8 ZNFX1 76 interacting genes: ADRA1B AGTR1 AP2B1 AQP4 ARRB2 ATXN1L BDKRB2 C1orf35 CACNA1A CD22 CD3D CDK11B CORO7 CSNK2B CTLA4 CXorf51A CXorf51B DAB2 DCX DPPA2 DVL2 EAF1 EHD2 EIF1AD FAM90A1 FURIN FXR2 GAK GRIN2B H2BC10 H2BC13 H2BC21 H2BC4 H2BC6 H2BC7 H2BC8 HEXIM2 HTR6 IKZF1 KCNJ11 KNOP1 LAMP1 LTB4R2 LY9 MAB21L3 MED4 MEGF10 MFAP1 MPP1 MTURN NAA11 NCOR2 NDRG1 NKAPD1 PRPF18 PRPF38A PRR13 PTS RALBP1 RNF111 RPL22 RPL38 RRP12 RSPH14 RUNDC3A SFRP4 STON2 SYNJ1 TASOR TBC1D5 TGOLN2 TMA16 UBC UTP25 ZBTB8A ZNF581
Entrez ID 84466 1173
HPRD ID 14384 03014
Ensembl ID ENSG00000145794 ENSG00000161203
Uniprot IDs Q96KG7 B4DNB9 E9PFW3 Q96CW1
PDB IDs 1H6E 6BNT 6URI
Enriched GO Terms of Interacting Partners?
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