SPG21 and CCDC102B

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

SPG21

CCDC102B

Gene Name spastic paraplegia 21 (autosomal recessive, Mast syndrome) coiled-coil domain containing 102B
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 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
Entrez ID 51324 79839
HPRD ID 10492 08038
Ensembl ID ENSG00000090487 ENSG00000150636
Uniprot IDs Q9NZD8 A1A4H1 Q68D86
PDB IDs
Enriched GO Terms of Interacting Partners?
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