NUDT21 and SHFM1

  • Number of citations of the paper that reports this interaction (PMID 21900206)
  • 27
  • Data Source:
  • BioGRID (two hybrid)

NUDT21

SHFM1

Gene Name nudix (nucleoside diphosphate linked moiety X)-type motif 21 split hand/foot malformation (ectrodactyly) type 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Attention deficit hyperactivity disorder ( 20732625)
  • Immunoglobulin A ( 20694011)
Protein-Protein Interactions 51 interactors: A2M ATXN1 CARM1 CLP1 CPSF6 CPSF7 CTNND2 DBN1 DNMT3L DYNC1I1 EED EEF1G EXOSC6 F13A1 FBN3 FLAD1 FUNDC2 GOLGA2 HSF4 IKZF1 ITCH JMJD1C KIAA1377 KIFAP3 MASP1 MYL6 NEDD4 NGEF NIF3L1 POLR2C PSMF1 PTN PYCR1 RBM48 RCC1 RNF19A RPLP1 SEMA5B SF3B1 SHC1 SHFM1 SLC44A1 SNCAIP SNRNP70 SRPK1 TCERG1 TLE1 TRA2A TRIM27 WWOX ZBTB48 7 interactors: BRCA1 BRCA2 MAP1LC3B NUDT21 PCID2 PSMD3 PSMD6
Entrez ID 11051 7979
HPRD ID 05400 03182
Ensembl ID ENSG00000167005
Uniprot IDs O43809 P60896 Q6IBB7
PDB IDs 2CL3 2J8Q 3BAP 3BHO 3MDG 3MDI 3N9U 3P5T 3P6Y 3Q2S 3Q2T 1IYJ 1MIU 1MJE 3T5X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  dync1i1  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Difference) ?
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  dync1i1  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Intersection) ?