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    CLAM cerebellar atrophy with progressive microcephaly [ Homo sapiens (human) ]

    Gene ID: 373073, updated on 2-Oct-2019

    Summary

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    Gene symbol
    CLAM
    Gene description
    cerebellar atrophy with progressive microcephaly
    Primary source
    MIM:608027
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PCH3

    Genomic context

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    Location:
    7q11-q21

    Bibliography

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    Related articles in PubMed

    1. A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21. Rajab A, et al. Neurology, 2003 May 27. PMID 12771259
    2. PCGF homologs, CBX proteins, and RYBP define functionally distinct PRC1 family complexes. Gao Z, et al. Mol Cell, 2012 Feb 10. PMID 22325352, Free PMC Article

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    cerebellar atrophy with progressive microcephaly

    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Property

    • phenotype only

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