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    SCKL3 Seckel syndrome 3 [ Homo sapiens (human) ]

    Gene ID: 386616, updated on 2-Oct-2019

    Summary

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    Gene symbol
    SCKL3
    Gene description
    Seckel syndrome 3
    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:
    14q23

    Bibliography

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    Related articles in PubMed

    1. Is the novel SCKL3 at 14q23 the predominant Seckel locus? Kilinç MO, et al. Eur J Hum Genet, 2003 Nov. PMID 14571270

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Seckel syndrome 3

    General gene information

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    Property

    • phenotype only

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