C14orf1 and PFN1

  • Number of citations of the paper that reports this interaction (PMID 16169070)
  • 531

C14orf1

PFN1

Gene Name chromosome 14 open reading frame 1 profilin 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 62 interactors: ALDH2 ANXA1 ANXA7 BAIAP2 BID BTBD2 CCDC106 CCL18 CDC42 CDK5RAP2 CELF3 CLN8 COX17 CRADD CREB1 CSTF2 DYNLL1 FAS FCGR2B FXR1 GADD45A GSK3B HMGB1 HNRNPH3 HNRNPUL1 HSPE1 HYLS1 KLHL20 LSM2 MAPK8IP2 MPHOSPH6 MRPL38 MRPS12 NAT9 NDUFA4L2 NR1H2 NSF PAFAH1B3 PCDHA4 PEX2 PFN1 PHYHIP POLE2 POLR2C POLR3F PPP1R8 PQBP1 RAB27A RPS6KA6 S100A8 SAT1 SEPHS1 SERPINB9 SNRPB SNRPG SULT1E1 TFG TK1 TSC22D1 TTR ZFP64 ZNF24 30 interactors: ACTA1 ACTB APBB1IP C14orf1 CMA1 CRMP1 DBN1 DLG5 DNM2 ENAH FMNL1 GPHN LRIF1 MLLT4 MYPOP NCK1 PIK3R1 RAD51 RHOQ SRPK1 STUB1 TLE1 UNC119 VASP VIPR1 WASF1 WASL WIPF2 XPO6 YWHAQ
Entrez ID 11161 5216
HPRD ID 05201 01452
Ensembl ID ENSG00000108518
Uniprot IDs Q6FII3 Q86TW5 Q9UKR5 P07737
PDB IDs 1AWI 1CF0 1CJF 1FIK 1FIL 1PFL 2PAV 2PBD 3CHW
Enriched GO Terms of Interacting Partners?
Tagcloud ?
a20t  adds  aggregation  als  amyotrophic  classic  dementia  demonstrating  displayed  e117g  fatal  frontotemporal  hallmark  heterogeneity  insoluble  lateral  meta  neurodegenerative  pathology  postmortem  profilin  published  q139l  rare  sclerosis  sequenced  tar  transfections  variant 
Tagcloud (Difference) ?
a20t  adds  aggregation  als  amyotrophic  classic  dementia  demonstrating  displayed  e117g  fatal  frontotemporal  hallmark  heterogeneity  insoluble  lateral  meta  neurodegenerative  pathology  postmortem  profilin  published  q139l  rare  sclerosis  sequenced  tar  transfections  variant 
Tagcloud (Intersection) ?