Gene content    
ESRRB (-- by HUGO)
estrogen-related receptor beta ------------------------------ (Previous names: deafness, autosomal r
--
Estrogen-Related Receptor Beta
ERR Beta-2
ESRL2
ERRbeta
NR3B2
Deafness, Autosomal Recessive 35
DFNB35
ERRbeta-2
ERR2
Estrogen-Related Nuclear Receptor Beta
ERRb
Nuclear Receptor ERRB2
Estrogen Receptor-Like 2
Orphan Nuclear Receptor
Nuclear Receptor Subfamily 3 Group B Member 2
Steroid Hormone Receptor ERR2
ERR-Beta
ERR
NCBI: 14q24.3    Ensembl: 14q24.3
ERR2_HUMANSize: 508 amino acidsMass: 56208 Da

  • Subcellular location: Nucleus (Potential) 1 PDB 3D structure from [IMAGE] and Proteopedia [IMAGE] for ESRRB: 1LO1 (3D) [IMAGE] Secondary accessions: A2VDJ2 B6ZGU4 Q5F0P7 Q5F0P8 Q9HCB4 Alternative splicing: 3 isoforms: O95718-1 O95718-2 O95718-3 Explore the universe of human pr
  • Subunit: Binds DNA as a monomer
  • Similarity:
    Belongs to the nuclear hormone receptor family. NR3 subfamily
                          
    Contains 1 nuclear receptor DNA-binding domain
  • Protein Domain/Family    
    Source ID Domain Name Type
    InterProIPR001723Str_hrmn_rcptSteroid hormone receptorFamily
    IPR008946Nucl_hormone_rcpt_ligand-bdSteroid nuclear receptor, ligand-bindingDomain
    BlocksIPB000003Retinoic acid receptor signatureRetinoic acid receptor signature
    IPB001723Steroid hormone receptor signatureSteroid hormone receptor signature

    Disorder & Mutation    
    Source Disease
    SWISS-PROTDefects in ESRRB are the cause of deafness autosomal recessive type 35 (DFNB35) [MIM:608565]. DFNB35 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information

    ESRRB cross reference    
    PubMed Entrez Gene NCKU SNP Nucleotide UniProt Genome Data Viewer HomoloGene