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WBSCR23 Williams-Beuren syndrome chromosome region 23 [ Homo sapiens (human) ]

Gene ID: 80112, discontinued on 10-Sep-2009

Summary

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Official Symbol
WBSCR23provided by HGNC
Official Full Name
Williams-Beuren syndrome chromosome region 23provided by HGNC
Primary source
HGNC:HGNC:16498
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This gene is intronless and mapped to the commonly deleted region for Williams-Beuren Syndrome. [provided by RefSeq]

Genomic context

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Location:
7q11.23
Exon count:
1
Sequence:
Chromosome: 7; NC_000007.12 (73584557..73585479)

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

General gene information

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Clone Names

  • FLJ22367

NCBI Reference Sequences (RefSeq)

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NEW Try the new Transcript table

RefSeqs of Annotated Genomes: Build 36.3 (NOTE: not current)

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

Reference assembly

Genomic

  1. NC_000007.12 Reference assembly

    Range
    73584557..73585479
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_040836.1 RNA Sequence

Alternate assembly (based on HuRef)

Genomic

  1. AC_000139.1 Alternate assembly (based on HuRef)

    Range
    69825859..69826781 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_040835.1 RNA Sequence

Alternate assembly (based on CRA_TCAGchr7v2)

Genomic

  1. AC_000068.1 Alternate assembly (based on CRA_TCAGchr7v2)

    Range
    73279693..73280615
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. XR_040834.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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