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    BEX2 brain expressed X-linked 2 [ Homo sapiens (human) ]

    Gene ID: 84707, updated on 2-Nov-2024

    Summary

    Official Symbol
    BEX2provided by HGNC
    Official Full Name
    brain expressed X-linked 2provided by HGNC
    Primary source
    HGNC:HGNC:30933
    See related
    Ensembl:ENSG00000133134 MIM:300691; AllianceGenome:HGNC:30933
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    BEX1; DJ79P11.1
    Summary
    This gene belongs to the brain expressed X-linked gene family. The encoded protein interacts with the transcription factor LIM domain only 2 in a DNA-binding complex that recognizes the E-box element and promotes transcription. This gene has been found to be a tumor suppressor that is silenced in human glioma. In breast cancer cells, this gene product modulates apoptosis in response to estrogen and tamoxifen, and enhances the anti-proliferative effect of tamoxifen. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]
    Annotation information
    Note: The BEX1 and BEX2 genes appear to have undergone gene conversion, exchanging bits of coding sequence with each other. This complicates determination of orthologs in other species. For this reason, gene name assignments may not be consistent between species. [06 Dec 2023]
    Expression
    Broad expression in brain (RPKM 60.5), thyroid (RPKM 40.0) and 14 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See BEX2 in Genome Data Viewer
    Location:
    Xq22.2
    Exon count:
    3
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (103309346..103310990, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (101756321..101757965, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (102564274..102565918, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene guanosine monophosphate reductase pseudogene Neighboring gene transcription elongation factor A like 5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20920 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:102585683-102586182 Neighboring gene transcription elongation factor A like 7 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:102603213-102603753 Neighboring gene uncharacterized LOC124905204 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:102610887-102612086 Neighboring gene transcription elongation factor A like 9

    Genomic regions, transcripts, and products

    Expression

    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables metal ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables molecular function inhibitor activity ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables signaling receptor binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Process Evidence Code Pubs
    involved_in apoptotic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in negative regulation of protein ubiquitination ISS
    Inferred from Sequence or Structural Similarity
    more info
     
    involved_in regulation of apoptotic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in regulation of apoptotic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of cell cycle IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in signal transduction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    Component Evidence Code Pubs
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     

    General protein information

    Preferred Names
    protein BEX2
    Names
    brain-expressed X-linked protein 2
    hBex2

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_016254.1 RefSeqGene

      Range
      5057..6701
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001168399.2NP_001161871.1  protein BEX2 isoform 1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
      Source sequence(s)
      AL133348, CD365521, DB498563
      Consensus CDS
      CCDS55467.1
      UniProtKB/Swiss-Prot
      Q9BXY8
      Related
      ENSP00000442521.1, ENST00000536889.1
      Conserved Domains (1) summary
      pfam04538
      Location:46156
      BEX; Brain expressed X-linked like family
    2. NM_001168400.2NP_001161872.1  protein BEX2 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) uses an alternate in-frame splice site in the 5' coding region compared to variant 1. This results in a shorter protein (isoform 2) compared to isoform 1.
      Source sequence(s)
      AL133348, BC015522, CB961647, DB498563
      UniProtKB/Swiss-Prot
      Q9BXY8
      Conserved Domains (1) summary
      pfam04538
      Location:45155
      BEX; Brain expressed X-linked like family
    3. NM_001168401.2NP_001161873.1  protein BEX2 isoform 3

      See identical proteins and their annotated locations for NP_001161873.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (3) has a shorter N-terminus, compared to isoform 1. Variants 3 and 4 encode the same isoform (3).
      Source sequence(s)
      BC015522, BU596902, CK001963
      Consensus CDS
      CCDS14505.1
      UniProtKB/Swiss-Prot
      B2R574, D3DXA2, F5H7H5, Q5JVV9, Q9BXY8
      Related
      ENSP00000361759.1, ENST00000372674.5
      Conserved Domains (1) summary
      pfam04538
      Location:14124
      BEX; Brain expressed X-linked like family
    4. NM_032621.4NP_116010.1  protein BEX2 isoform 3

      See identical proteins and their annotated locations for NP_116010.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (3) has a shorter N-terminus, compared to isoform 1. Variants 3 and 4 encode the same isoform (3).
      Source sequence(s)
      BC015522, BU569325
      Consensus CDS
      CCDS14505.1
      UniProtKB/Swiss-Prot
      B2R574, D3DXA2, F5H7H5, Q5JVV9, Q9BXY8
      Related
      ENSP00000361762.3, ENST00000372677.8
      Conserved Domains (1) summary
      pfam04538
      Location:14124
      BEX; Brain expressed X-linked like family

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      103309346..103310990 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      101756321..101757965 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)