C11orf49 and PSMA1

  • Number of citations of the paper that reports this interaction (PubMedID 16169070)
  • 820

C11orf49

PSMA1

Description chromosome 11 open reading frame 49 proteasome 20S subunit alpha 1
Image No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Alzheimer's disease or fasting glucose levels (pleiotropy) ( 30805717)
  • Autism spectrum disorder or schizophrenia ( 28540026)
  • D-dimer levels ( 21502573)
  • Intraocular pressure ( 29617998)
  • Neurociticism ( 29500382)
  • Alzheimer's disease (cognitive decline) ( 23535033)
  • Bipolar disorder ( 31043756)
  • Diastolic blood pressure ( 27841878)
  • High chromosomal aberration frequency (total) ( 31586183)
  • Systolic blood pressure ( 27841878)
  • Vitamin D levels ( 25208829)
Interacting Genes 12 interacting genes: ARHGEF15 CDC16 GSR PNMA5 PSMA1 RAB17 RAB29 RBM48 RPL8 RPS3A UBE3A UBQLN4 89 interacting genes: ABCD3 ABI3 ACTN1 APIP APP BLZF1 C11orf49 CALCOCO2 CBS CCDC102B CCDC85B CCNH CDA CEP70 CEP72 COIL DLEU1 EHMT2 GNPTAB GOLGA2 HOMER3 HSD17B14 IFT20 IKZF1 IKZF3 INO80E KCTD1 KCTD17 KCTD9 KRT15 KRT31 KRT38 KRT40 KRTAP5-9 LDB1 LDOC1 LZTS2 MAD1L1 MAPRE1 MAPRE3 MCM6 MID2 MKRN3 MLH1 MRFAP1L1 MT-CO2 MTUS2 NECAB2 NMI NOP53 NOTCH2NLA PLK1 PNMA1 PNMA2 PNMA5 POMP PPCDC PRDM14 PRKN PSMA2 PSMA3 PSMA4 PSMA7 PSMB1 PSMB10 PSMB2 PSMB5 RAD54B REL ROPN1 SFMBT1 SH3BP4 SH3GLB1 SSX2IP TCF12 TCF4 TDO2 TNFAIP1 TNR TRAF1 TRIM10 TRIM23 TRIM27 TRIM42 TSC22D4 UBXN11 VCP VIM ZFAND1
Entrez ID 79096 5682
HPRD ID 08332 04170
Ensembl ID ENSG00000149179 ENSG00000129084
Uniprot IDs B4DUV7 Q9H6J7 B4E0X6 P25786
PDB IDs 4R3O 4R67 5A0Q 5GJQ 5GJR 5L4G 5LE5 5LEX 5LEY 5LEZ 5LF0 5LF1 5LF3 5LF4 5LF6 5LF7 5LN3 5M32 5T0C 5T0G 5T0H 5T0I 5T0J 5VFO 5VFP 5VFQ 5VFR 5VFS 5VFT 5VFU 6AVO 6E5B 6MSB 6MSD 6MSE 6MSG 6MSH 6MSJ 6MSK 6R70 6REY 6RGQ
Enriched GO Terms of Interacting Partners?
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