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    HLN2 Huntington-like neurodegenerative disorder 2 [ Homo sapiens ]

    Gene ID: 53369, updated on 6-May-2012
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    Summary

    Gene symbol
    HLN2
    Gene description
    Huntington-like neurodegenerative disorder 2
    Primary source
    MIM:604802
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    HDL3
    Annotation information
    Annotation category: not annotated on reference assembly
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    Genomic context

    Location :
    4p15.3
    See HLN2 in MapViewer
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    Bibliography

    Related articles in PubMed

    1. Biglycan, a vascular proteoglycan, binds differently to HDL2 and HDL3: role of apoE. Olin KL, et al. Arterioscler Thromb Vasc Biol, 2001 Jan. PMID 11145944.
    2. Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3. Kambouris M, et al. Am J Hum Genet, 2000 Feb. PMID 10677304.

    GeneRIFs: Gene References Into Functions What's a GeneRIF?

    Submit: New GeneRIF Correction
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    Phenotypes

    Huntington disease-like 3

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    Interactions

    Products Interactant Other Gene Complex Source Pubs Description
    BioGRID:119758 BioGRID:107102 BGN    BioGRID  PubMed Reconstituted Complex 
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    General gene information

    Markers

    Property

    • phenotype only
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    Additional Links

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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