CCDC102B and SPG21

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

CCDC102B

SPG21

Gene Name coiled-coil domain containing 102B spastic paraplegia 21 (autosomal recessive, Mast syndrome)
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 52 interactors: ABI2 AK8 ARL4A ARL4D BYSL C20orf195 CCDC101 CCDC120 CCDC33 CCHCR1 CDK18 CEP19 CEP57L1 EHHADH ENKD1 EXOC5 FAM127B FAM127C FAM161A FBF1 GEM GOPC HMG20B KIFC3 LENG1 LMO4 LNX1 MAB21L2 MAGOHB MARK1 MCM7 MOS NIF3L1 NXT2 PNMA5 POP5 PPP1R18 PSMA1 RCOR3 RSPH14 SDCBP SFN SLIRP SPG21 SYCE1 TPM3 TRIM27 TRIM54 WDYHV1 ZNF20 ZNF250 ZNF572 37 interactors: AGTRAP AKIRIN2 ARL6IP1 ATPAF2 CCDC102B CCDC33 CD4 CMTM5 CRYAA CTPS2 CUTC DTX2 DTX3L EFHC2 FAM114A1 GGA2 GSK3A IKZF3 INCA1 KRT15 MID2 MTMR9 PRPS1 RABAC1 REEP6 RTN4 S100B SPRED2 TCF12 TCF4 TFG TRAF1 TRAF2 TRIM23 TRIM54 TRIM9 ZNF263
Entrez ID 79839 51324
HPRD ID 08038 10492
Ensembl ID ENSG00000150636 ENSG00000090487
Uniprot IDs A1A4H1 Q68D86 Q9NZD8
PDB IDs
Enriched GO Terms of Interacting Partners?
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