BAIT
NRIP1
RIP140
nuclear receptor interacting protein 1
GO Process (6)
GO Function (8)
GO Component (4)
Gene Ontology Biological Process
- androgen receptor signaling pathway [NAS]
- circadian regulation of gene expression [IMP]
- circadian rhythm [IEP]
- negative regulation of transcription from RNA polymerase II promoter [IDA]
- positive regulation of transcription from RNA polymerase II promoter [IDA]
- positive regulation of transcription, DNA-templated [NAS]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
SESTD1
SOLO
SEC14 and spectrin domains 1
GO Process (0)
GO Function (11)
GO Component (1)
Gene Ontology Molecular Function- 1-phosphatidylinositol binding [IDA]
- phosphatidic acid binding [IDA]
- phosphatidylcholine binding [IDA]
- phosphatidylinositol-3,4-bisphosphate binding [IDA]
- phosphatidylinositol-3,5-bisphosphate binding [IDA]
- phosphatidylinositol-3-phosphate binding [IDA]
- phosphatidylinositol-4,5-bisphosphate binding [IDA]
- phosphatidylinositol-4-phosphate binding [IDA]
- phosphatidylinositol-5-phosphate binding [IDA]
- phosphatidylserine binding [IDA]
- protein binding [IPI]
- 1-phosphatidylinositol binding [IDA]
- phosphatidic acid binding [IDA]
- phosphatidylcholine binding [IDA]
- phosphatidylinositol-3,4-bisphosphate binding [IDA]
- phosphatidylinositol-3,5-bisphosphate binding [IDA]
- phosphatidylinositol-3-phosphate binding [IDA]
- phosphatidylinositol-4,5-bisphosphate binding [IDA]
- phosphatidylinositol-4-phosphate binding [IDA]
- phosphatidylinositol-5-phosphate binding [IDA]
- phosphatidylserine binding [IDA]
- protein binding [IPI]
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