Gene Ontology annotation through association of InterPro records with GO terms.

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt.

Gene Ontology annotation based on curation of immunofluorescence data

Quantitative interaction proteomics and genome-wide profiling of epigenetic histone marks and their readers.

CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment.

A human interactome in three quantitative dimensions organized by stoichiometries and abundances.

DNA Repair Network Analysis Reveals Shieldin as a Key Regulator of NHEJ and PARP Inhibitor Sensitivity.

FAM35A associates with REV7 and modulates DNA damage responses of normal and BRCA1-defective cells.

CHAMP1 binds to REV7/FANCV and promotes homologous recombination repair.

De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.

Deep research summary for CHAMP1

CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair.

Dynamic feature of mitotic arrest deficient 2-like protein 2 (MAD2L2) and structural basis for its interaction with chromosome alignment-maintaining phosphoprotein (CAMP).

CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency.

CHAMP1 complex promotes heterochromatin assembly and reduces replication stress.

CHAMP1 is an essential regulator for human myoblast fusion and muscle development.

CHAMP1 source, ontology and primary-access evidence