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RPS3A and FANCC
Data Source:
BioGRID
(two hybrid)
RPS3A
FANCC
Description
ribosomal protein S3A
FA complementation group C
Image
No pdb structure
GO Annotations
Cellular Component
Nucleus
Nucleoplasm
Nucleolus
Cytoplasm
Endoplasmic Reticulum
Cytosol
Focal Adhesion
Cytosolic Small Ribosomal Subunit
Extracellular Exosome
Ribonucleoprotein Complex
Nucleus
Nucleoplasm
Cytoplasm
Cytosol
Fanconi Anaemia Nuclear Complex
Molecular Function
RNA Binding
Structural Constituent Of Ribosome
Protein Binding
MRNA 5'-UTR Binding
Protein Binding
Biological Process
Nuclear-transcribed MRNA Catabolic Process, Nonsense-mediated Decay
Translation
Translational Initiation
SRP-dependent Cotranslational Protein Targeting To Membrane
Viral Transcription
Cell Differentiation
Negative Regulation Of Apoptotic Process
Myeloid Cell Homeostasis
DNA Repair
Nucleotide-excision Repair
Germ Cell Development
Removal Of Superoxide Radicals
Cellular Response To Oxidative Stress
Interstrand Cross-link Repair
Brain Morphogenesis
Protein-containing Complex Assembly
Neuronal Stem Cell Population Maintenance
Pathways
L13a-mediated translational silencing of Ceruloplasmin expression
Peptide chain elongation
SRP-dependent cotranslational protein targeting to membrane
SRP-dependent cotranslational protein targeting to membrane
Viral mRNA Translation
Selenocysteine synthesis
Major pathway of rRNA processing in the nucleolus and cytosol
Translation initiation complex formation
Formation of a pool of free 40S subunits
Formation of the ternary complex, and subsequently, the 43S complex
Ribosomal scanning and start codon recognition
GTP hydrolysis and joining of the 60S ribosomal subunit
Eukaryotic Translation Termination
Regulation of expression of SLITs and ROBOs
Response of EIF2AK4 (GCN2) to amino acid deficiency
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
Fanconi Anemia Pathway
TP53 Regulates Transcription of DNA Repair Genes
Drugs
Diseases
Fanconi anemia
GWAS
HDL cholesterol (
20686565
)
Birth weight (
31043758
)
Hematocrit (
32888494
)
Offspring birth weight (
31043758
)
Polycystic ovary syndrome (
26284813
)
Interacting Genes
18 interacting genes:
ATF7IP
C11orf49
CCDC50
CHN1
CREB3
DDIT3
DUX4
EDEM2
FANCC
HGS
HSP90AA1
NEDD4
PARP1
SAP18
SOD2
TOE1
UBE2I
VDAC2
54 interacting genes:
APC
AZIN1
BMPR1A
BUB1
CAPN10
CCNA2
CCND1
CDK1
CTBP1
DLC1
DNAJB1
EGFR
FANCA
FANCD2
FANCE
FANCF
FANCG
FBXW7
GSTP1
HSP90AA1
HSP90B1
HSPA1A
HSPA4
HSPA8
IK
KRAS
KRT1
MEOX2
MLH3
MT-ATP6
MUTYH
NRAS
PDGFRL
PIK3CA
PMS2
POR
PRDX3
PRPF31
PTPN12
PTPRJ
RB1
RPL18
RPS3A
SMAD4
SPTA1
SPTAN1
SRC
STAT1
STMN1
STMN2
TCERG1
TGFBR2
USP14
ZBTB32
Entrez ID
6189
2176
HPRD ID
01606
01967
Ensembl ID
ENSG00000145425
ENSG00000158169
Uniprot IDs
B7Z3M5
P61247
A0A024R9N2
A0A087WW44
B4E3W2
Q00597
PDB IDs
4UG0
4V6X
5A2Q
5AJ0
5FLX
5LKS
5OA3
5T2C
5VYC
6EK0
6FEC
6G18
6G4S
6G4W
6G51
6G53
6G5H
6G5I
6IP5
6IP6
6IP8
6OLE
6OLF
6OLG
6OLI
6OLZ
6OM0
6OM7
6QZP
6XA1
6Y0G
6Y2L
6Y57
6YBD
6YBW
6Z6L
6Z6M
6Z6N
6ZLW
6ZM7
6ZME
6ZMI
6ZMO
6ZMT
6ZMW
6ZN5
6ZOJ
6ZOK
6ZON
6ZP4
6ZVH
6ZVJ
7A09
7K5I
Enriched GO Terms of Interacting Partners
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