ACTN3 and C1orf94

  • Data Source:
  • BioGRID (two hybrid)

ACTN3

C1orf94

Description actinin alpha 3 chromosome 1 open reading frame 94
Image No pdb structure
GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Bipolar disorder ( 21926972)
  • Frontotemporal dementia with GRN mutation ( 29724592)
  • Generalized epilepsy ( 22949513)
  • Lateral ventricle temporal horn volume ( 31530798)
  • Pediatric nonalcoholic steatohepatitis ( 28918882)
  • Sleep duration (short sleep) ( 30846698)
Interacting Genes 61 interacting genes: ABI3 ACTN1 ACTN2 ACTN4 ADORA2A ASB9 ATP23 BRCA1 C1orf94 C20orf85 C2CD6 CADPS CTAG1A CTAG1B CTDSP1 CXCL5 DDAH2 DUX1 DUX4L9 ECM1 FAM90A1 GLIS2 HGS HOXD12 HSF2BP IVD KCTD6 KRT6C LHX3 LINC01554 LNX1 MAGEA6 MICALL2 MYOT MYOZ1 MYPN NDUFAB1 NEBL NKAPD1 NRAP ODF3B PCCB PKP2 PLEKHG2 POU6F2 PPP1R18 PTK6 REL RNF111 RTP5 SNAI1 SOHLH1 SUMO1P1 SYNPO2L TRAF1 TRAF2 TRIM29 TTN USP2 ZNF343 ZNF426 89 interacting genes: ACTN3 AKAP9 ATRIP ATXN1 ATXN1L BANP BOLA1 BOLA2 BOLA2B BOLL BYSL C1orf109 CAMK2A CARD9 CCHCR1 CCNJL CDKN2D CFAP206 CHERP CLK1 CRK CRYBA4 DAB1 DAZAP2 DGCR6 DMRTB1 DOK6 DTX2 FAM168A FHL3 GCC1 GORASP2 GRB2 GSE1 HGS HNRNPF HSF2BP INTS11 IPO11 KLHL32 KRTAP6-2 KRTAP7-1 KRTAP8-1 LCE2C LMO2 MAGED1 MAPK1IP1L MAPK9 MEIS2 MVP NFKBID NGB NR3C1 OAZ3 OIP5 PITX1 PLA2G10 PLEKHB2 PRKAG1 PROP1 PRR20A PRR20B PRR20C PRR20D PRR20E R3HDM2 RAD51D RBFOX1 RBFOX2 RBM47 RBPMS RFX2 RHOXF2 ROR2 SMAP2 SS18L1 TBX6 TENT5D TLE5 TNPO2 TNS2 TSC1 TXNDC9 UBQLN2 UBQLN4 USO1 VENTX VPS37C YES1
Entrez ID 89 84970
HPRD ID 02148 11310
Ensembl ID ENSG00000248746 ENSG00000142698
Uniprot IDs A0A087WSZ2 B4DZQ2 Q08043 Q6P1W5
PDB IDs 1TJT 1WKU 3LUE
Enriched GO Terms of Interacting Partners?
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