BAIT
C21ORF59
C21orf48, CILD26, FBB18
chromosome 21 open reading frame 59
GO Process (0)
GO Function (0)
GO Component (2)
Homo sapiens
PREY
FMN2
RP11-90L13.1
formin 2
GO Process (11)
GO Function (1)
GO Component (5)
Gene Ontology Biological Process
- cellular response to DNA damage stimulus [IMP]
- cellular response to hypoxia [IMP]
- establishment of meiotic spindle localization [ISS]
- formin-nucleated actin cable assembly [ISS]
- homologous chromosome movement towards spindle pole involved in homologous chromosome segregation [ISS]
- intracellular transport [ISS]
- negative regulation of apoptotic process [IMP]
- negative regulation of protein catabolic process [IMP]
- oogenesis [ISS]
- polar body extrusion after meiotic divisions [ISS]
- vesicle-mediated transport [ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
Two-hybrid
Bait protein expressed as a DNA binding domain (DBD) fusion and prey expressed as a transcriptional activation domain (TAD) fusion and interaction measured by reporter gene activation.
Publication
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Down syndrome (DS) is caused by human chromosome 21 (HSA21) trisomy. It is characterized by a poorly understood intellectual disability (ID). We studied two mouse models of DS, one with an extra copy of the <i>Dyrk1A</i> gene (189N3) and the other with an extra copy of the mouse Chr16 syntenic region (Dp(16)1Yey). RNA-seq analysis of the transcripts deregulated in the ... [more]
Life Sci Alliance Aug. 01, 2022; 5(12); [Pubmed: 35914814]
Throughput
- High Throughput
Curated By
- BioGRID