FLOT1 and CCDC102B

  • Data Source:
  • BioGRID (two hybrid)

FLOT1

CCDC102B

Description flotillin 1 coiled-coil domain containing 102B
Image No pdb structure No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Autism spectrum disorder or schizophrenia ( 28540026)
  • Blood protein levels ( 28240269)
  • Cutaneous lupus erythematosus ( 25827949)
  • Decreased fine motor function in Charcot-Marie-Tooth disease 1A (eating with utensils) ( 30958311)
  • General cognitive ability ( 29844566)
  • Handedness (non-right-handed vs right-handed) ( 31504236)
  • Schizophrenia ( 30285260)
  • Sleep duration ( 25469926)
  • Ulcerative colitis ( 20848476)
  • Caudate activity during reward ( 28927378)
  • Liver enzyme levels (alanine transaminase) ( 24124411)
  • Myopic maculopathy ( 29725004)
  • Pursuit maintenance gain ( 29064472)
  • Pursuit maintenance gain in psychotic disorders ( 29064472)
  • Rostral anterior cingulate cortex volume ( 31530798)
Interacting Genes 23 interacting genes: APP ARG1 AURKB BANP CAPN10 CBL CCDC102B COX5B FAM90A1 FLOT2 FYN GOLM1 HGS INCENP NGB NME7 PSMD4 SHBG SORBS1 SORBS2 SORBS3 SRPK1 UBC 102 interacting genes: ABI2 AK8 ANKRD23 ARL4A ARL4D BYSL C20orf202 CACNB4 CAPN3 CCDC120 CCDC187 CCDC33 CCHCR1 CDK18 CEP19 CEP57L1 CWF19L2 DISC1 DOCK10 EFHC2 EHHADH ENKD1 EXOC5 FAM161A FAM217B FBF1 FH FLOT1 FNDC11 GEM GOPC HMG20B IKZF3 KIFC3 KPNA3 KRT75 KRTAP13-3 LENG1 LMO4 LNX1 LZTS1 MAB21L2 MAGOHB MARK1 MCM7 MEOX1 MEOX2 MFAP1 MOS MSX2 NIF3L1 NME4 NTAQ1 NXT2 PFKFB4 PHAF1 PICK1 PNMA5 POMC POP5 PPP1R13B PPP1R18 PRPF18 PSMA1 RASAL3 RCOR3 RSPH14 RTL8A RTL8B RTL8C SDCBP SFN SGF29 SH3RF2 SLIRP SMARCD1 SNAPIN SORBS3 SPATA18 SPATA2 SPG21 SYCE1 SYT17 TCEANC TCP10L TFIP11 TNNI1 TPM3 TRIM27 TRIM54 TSGA10IP TTC23 VPS52 ZBTB32 ZBTB42 ZC2HC1C ZNF20 ZNF250 ZNF572 ZNF620 ZNF688 ZNF774
Entrez ID 10211 79839
HPRD ID 06105 08038
Ensembl ID ENSG00000137312 ENSG00000150636
Uniprot IDs O75955 Q5ST80 Q68D86
PDB IDs
Enriched GO Terms of Interacting Partners?
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