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Wbscr27 Gene Detail
Summary
  • Symbol
    Wbscr27
  • Name
    Williams Beuren syndrome chromosome region 27 (human)
  • Synonyms
    MGC:8159
  • Feature Type
    protein coding gene
  • IDs
    MGI:1933146
    NCBI Gene: 79565
Location & Maps
more
  • Sequence Map
    Chr5:134932368-134942637 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      10270 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 5, 74.89 cM
  • Mapping Data
    4 experiments
Homology
more
  • Human Ortholog
    WBSCR27, Williams Beuren syndrome chromosome region 27
  • Vertebrate Orthologs
    9
  • Human Ortholog
    WBSCR27, Williams Beuren syndrome chromosome region 27
    Orthology source: HomoloGene, HGNC
  • Links
    NCBI Gene ID: 155368
    neXtProt AC: NX_Q8N6F8
    UniProt: Q8N6F8

  • Chr Location
    7q11.23; chr7:73834590-73842527 (-)  GRCh38.p7

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 phenotype references
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000025980 VEGA Gene Model | MGI Sequence Detail 10270 C57BL/6J ±  kb
transcript OTTMUST00000064086 VEGA | MGI Sequence Detail 2808 Not Applicable  
polypeptide OTTMUSP00000031784 VEGA | MGI Sequence Detail 238 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    52 from dbSNP Build 142
Protein
Information
less
  • UniProt
    8 Sequences
  • InterPro Domains
    IPR029063 S-adenosyl-L-methionine-dependent methyltransferase
Molecular
Reagents
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  • All nucleic 6
    Genomic 1
    cDNA 5

    Microarray probesets 3
Other
Accession IDs
less
MGI:2141200
References
more
  • Summaries
    All 26
    Diseases 1
    Phenotypes 7
  • Earliest
    J:73830 DeSilva U, et al., Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. Genome Res. 2002 Jan;12(1):3-15
  • Latest
    J:216195 Segura-Puimedon M, et al., Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder. Hum Mol Genet. 2014 Dec 15;23(24):6481-94

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory