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    SLI1 Specific language impairment QTL, 1 [ Homo sapiens (human) ]

    Gene ID: 171013, updated on 7-Dec-2024

    Summary

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    Gene symbol
    SLI1
    Gene description
    Specific language impairment QTL, 1
    See related
    MIM:606711
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

    Genomic context

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    Location:
    16q

    Bibliography

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    Related articles in PubMed

    1. Association of D16S515 microsatellite with specific language impairment on Robinson Crusoe Island, an isolated Chilean population: a possible key to understanding language development. Villanueva P, et al. Hum Biol, 2010 Aug. PMID 21082909
    2. A genomewide scan identifies two novel loci involved in specific language impairment. SLI Consortium. Am J Hum Genet, 2002 Feb. PMID 11791209, Free PMC Article

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. The analysis of microsatellite marker D16S515, located in locus SLI1, demonstrated that the 230-bp allele was correlated with Specific language impairment and that the 232-bp allele was correlated with normal language development.
      Title: Association of D16S515 microsatellite with specific language impairment on Robinson Crusoe Island, an isolated Chilean population: a possible key to understanding language development.
    Submit: New GeneRIF Correction

    Phenotypes

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    Specific language impairment QTL, 1

    General gene information

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    Markers

    Property

    • phenotype only

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