HAX1 and BIRC3

  • Number of citations of the paper that reports this interaction (PMID 25275296)
  • 0
  • Data Source:
  • BioGRID (pull down, pull down)

HAX1

BIRC3

Gene Name HCLS1 associated protein X-1 baculoviral IAP repeat containing 3
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 23 interactors: ABCB1 ABCB11 ABCB4 BIRC3 CTTN DGKD EIF3F HCLS1 HNF4G IL1A KIAA0513 MAPK10 NEDD4L PKD2 POLR1D PPP3CC RBX1 RPA1 STAT5B SVIL YWHAQ ZNF420 ZNRD1 37 interactors: BCL10 BIRC5 CASP3 CASP7 CASP9 CD40 CYFIP2 DIABLO DZIP3 GSPT1 HAX1 HTRA2 IKBKE IKBKG MAP3K14 MBTPS1 PACS2 RAF1 RCHY1 RIPK1 RIPK2 RIPK3 RIPK4 SNX7 SPHK1 SUMO1 TRAF1 TRAF2 TRAF3 UBE2D1 UBE2D2 UBE2D3 UBE2I UBE2N UBE2Q2 UBE2V1 USP19
Entrez ID 10456 330
HPRD ID 12075 03426
Ensembl ID ENSG00000143575 ENSG00000023445
Uniprot IDs O00165 Q13489
PDB IDs 2UVL 3EB5 3EB6 3M0A 3M0D
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1222a  abolishing  aciduria  arg408gly  atp2a2  atrophy  biochemically  caseinolytic  cataracts  cerebellar  clpb  congenital  deleterious  disability  encephalopathy  exome  intellectual  kostmann  methylglutaconic  movement  neutropenia  nonprogressive  overlapping  peptidase  prenatal  sanger  scn  unrelated  zebrafish 
binet  biology  briefer  chinese  cll  concurrent  confounded  consecutive  descent  diverse  etiology  european  fludarabine  frequencies  germline  give  ighv  insights  lymphocytic  mutated  mutations  myd88  notch1  persons  predominately  sf3b1  stratification  tp53  un 
Tagcloud (Difference) ?
1222a  abolishing  aciduria  arg408gly  atp2a2  atrophy  biochemically  caseinolytic  cataracts  cerebellar  clpb  congenital  deleterious  disability  encephalopathy  exome  intellectual  kostmann  methylglutaconic  movement  neutropenia  nonprogressive  overlapping  peptidase  prenatal  sanger  scn  unrelated  zebrafish 
binet  biology  briefer  chinese  cll  concurrent  confounded  consecutive  descent  diverse  etiology  european  fludarabine  frequencies  germline  give  ighv  insights  lymphocytic  mutated  mutations  myd88  notch1  persons  predominately  sf3b1  stratification  tp53  un 
Tagcloud (Intersection) ?