BAIT
CLDN19
HOMG5
claudin 19
GO Process (1)
GO Function (1)
GO Component (3)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
PKD2L1
PCL, PKD2L, PKDL, TRPP3
polycystic kidney disease 2-like 1
GO Process (9)
GO Function (13)
GO Component (9)
Gene Ontology Biological Process
- cation transport [ISS]
- cellular response to acidic pH [ISS]
- detection of chemical stimulus involved in sensory perception of sour taste [ISS]
- detection of mechanical stimulus [IBA]
- potassium ion transmembrane transport [IDA]
- protein homotrimerization [IDA]
- sensory perception of sour taste [IMP]
- smoothened signaling pathway [ISS]
- sodium ion transmembrane transport [IDA]
Gene Ontology Molecular Function- alpha-actinin binding [IPI]
- calcium activated cation channel activity [IDA]
- calcium channel activity [IBA, IDA]
- calcium ion binding [IDA, ISS]
- calcium-activated potassium channel activity [IDA]
- cation channel activity [IDA]
- cation transmembrane transporter activity [ISS]
- cytoskeletal protein binding [IPI]
- identical protein binding [ISS]
- muscle alpha-actinin binding [IPI]
- protein binding [IPI]
- sodium channel activity [IDA]
- sour taste receptor activity [ISS]
- alpha-actinin binding [IPI]
- calcium activated cation channel activity [IDA]
- calcium channel activity [IBA, IDA]
- calcium ion binding [IDA, ISS]
- calcium-activated potassium channel activity [IDA]
- cation channel activity [IDA]
- cation transmembrane transporter activity [ISS]
- cytoskeletal protein binding [IPI]
- identical protein binding [ISS]
- muscle alpha-actinin binding [IPI]
- protein binding [IPI]
- sodium channel activity [IDA]
- sour taste receptor activity [ISS]
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
Widespread macromolecular interaction perturbations in human genetic disorders.
How disease-associated mutations impair protein activities in the context of biological networks remains mostly undetermined. Although a few renowned alleles are well characterized, functional information is missing for over 100,000 disease-associated variants. Here we functionally profile several thousand missense mutations across a spectrum of Mendelian disorders using various interaction assays. The majority of disease-associated alleles exhibit wild-type chaperone binding profiles, ... [more]
Cell Apr. 23, 2015; 161(3);647-60 [Pubmed: 25910212]
Throughput
- High Throughput
Curated By
- BioGRID