{
    "uniprot_canonical_ac": "A2A654-1", 
    "publication_count": 3, 
    "reported_interactions": 0, 
    "record_type": "protein", 
    "predicted_glycosites": 0, 
    "protein_names_refseq": "fetal Alzheimer antigen; nucleosome-remodeling factor subunit BPTF isoform 2", 
    "refseq_ac": "NP_789820.2", 
    "reported_n_glycosites": 0, 
    "refseq_name": "nucleosome-remodeling factor subunit BPTF isoform 2", 
    "record_id": "A2A654-1", 
    "protein_names_uniprotkb": "Bromodomain PHD finger transcription factor", 
    "pathway": "", 
    "function": "An essential requirement of the chromatin remodeler BPTF and NURF for activation of 'stemness' gene-expression programs and proper function of adult HSCs., [RefSeq]; This study implicates BPTF in maintaining the unique epigenetic state of mammary gland stem cells., [RefSeq]", 
    "protein_name": "Bromodomain PHD finger transcription factor", 
    "reported_mutagensis": 0, 
    "reported_phosphosites": 0, 
    "reported_o_glycosites_with_glycan": 0, 
    "tax_id": 10090, 
    "organism": "Mus musculus", 
    "disease": "Alzheimer's disease (Disease Ontology:DOID:10652); amyotrophic lateral sclerosis (Disease Ontology:DOID:332)", 
    "reported_glycation": 0, 
    "reported_snv": 0, 
    "mass": 333228.0, 
    "gene_names_uniprotkb": "Bptf", 
    "reported_n_glycosites_with_glycan": 0, 
    "reported_o_glycosites": 0, 
    "gene_names_refseq": "9430093H17Rik; Fa; Falz; Bptf", 
    "gene_name": "Bptf"
}