BAIT
DYRK1A
DYRK, DYRK1, HP86, MNB, MNBH, MRD7
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
GO Process (9)
GO Function (7)
GO Component (3)
Gene Ontology Biological Process
- circadian rhythm [ISS]
- mitotic cell cycle [TAS]
- negative regulation of DNA damage response, signal transduction by p53 class mediator [ISS]
- nervous system development [TAS]
- peptidyl-threonine phosphorylation [ISS]
- peptidyl-tyrosine phosphorylation [IDA, ISS]
- positive regulation of protein deacetylation [ISS]
- protein autophosphorylation [ISS]
- protein phosphorylation [ISS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
SULF1
HSULF-1, SULF-1
sulfatase 1
GO Process (21)
GO Function (2)
GO Component (6)
Gene Ontology Biological Process
- bone development [ISS]
- cartilage development [ISS]
- chondrocyte development [ISS]
- embryonic skeletal system development [ISS]
- esophagus smooth muscle contraction [ISS]
- glial cell-derived neurotrophic factor receptor signaling pathway [ISS]
- glomerular basement membrane development [ISS]
- glomerular filtration [ISS]
- heparan sulfate proteoglycan metabolic process [IDA, NAS]
- innervation [ISS]
- kidney development [ISS]
- negative regulation of angiogenesis [IDA]
- negative regulation of cell migration [IMP]
- negative regulation of endothelial cell proliferation [IDA]
- negative regulation of fibroblast growth factor receptor signaling pathway [IMP, ISS]
- negative regulation of prostatic bud formation [ISS]
- positive regulation of BMP signaling pathway [IMP]
- positive regulation of Wnt signaling pathway [IDA]
- positive regulation vascular endothelial growth factor production [ISS]
- regulation of fibroblast growth factor receptor signaling pathway [IMP]
- vascular endothelial growth factor receptor signaling pathway [IDA]
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