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

Gene ID: 171013, updated on 16-Aug-2019

Summary

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Gene symbol
SLI1
Gene description
Specific language impairment QTL, 1
Primary source
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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