{
    "uniprot_canonical_ac": "A2AI08-1", 
    "publication_count": 11, 
    "reported_interactions": 0, 
    "record_type": "protein", 
    "predicted_glycosites": 0, 
    "protein_names_refseq": "taperin", 
    "refseq_ac": "NP_780495.2", 
    "reported_n_glycosites": 0, 
    "refseq_name": "taperin", 
    "record_id": "A2AI08-1", 
    "protein_names_uniprotkb": "Taperin", 
    "pathway": " (mmu:97031)", 
    "function": "Stereocilia lacking GRXCR2 are longer than normal and disorganized due to the mislocalization of taperin, which could modulate the actin cytoskeleton in stereocilia., [RefSeq]; Taperin plays an important role in maintenance of hair cell stereocilia., [RefSeq]; Tprn is critical to the retention of the integrity of the stereociliary rootlet. Loss of Tprn in Tprn-null mice caused the disruption of the stereociliary rootlet, which resulted in damage to stereociliary bundles and hearing impairments., [RefSeq]", 
    "protein_name": "Taperin", 
    "reported_mutagensis": 0, 
    "reported_phosphosites": 6, 
    "reported_o_glycosites_with_glycan": 0, 
    "tax_id": 10090, 
    "organism": "Mus musculus", 
    "disease": "autosomal recessive nonsyndromic deafness 79 (Disease Ontology:DOID:0110526)", 
    "reported_glycation": 0, 
    "reported_snv": 0, 
    "mass": 80089.0, 
    "gene_names_uniprotkb": "Tprn", 
    "reported_n_glycosites_with_glycan": 0, 
    "reported_o_glycosites": 0, 
    "gene_names_refseq": "C430004E15Rik; C87750; Tprn", 
    "gene_name": "Tprn"
}