About   Help   FAQ
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

  • Chr Location
    7q11.23; chr7:73834590-73842525 (-)  GRCh38.p2

Human Diseases
less
  • References
    3 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    7 phenotype references
  • All Mutations and Alleles
    7
  • Gene trapped
    4
  • Targeted
    3
  • Genomic Mutations
    2 involving Wbscr27
  • Incidental Mutations
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
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
less
  • All nucleic 6
    Genomic 1
    cDNA 5

    Microarray probesets 3
Other
Accession IDs
less
MGI:2141200
References
more
  • Summaries
    All 23
    Diseases 3
    Gene Ontology 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:153498 Diez-Roux G, et al., A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol. 2011;9(1):e1000582

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/22/2016
MGI 6.06
The Jackson Laboratory