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    ERDA1 expanded repeat domain, CAG/CTG 1 [ Homo sapiens (human) ]

    Gene ID: 9030, updated on 17-Aug-2024

    Summary

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    Official Symbol
    ERDA1provided by HGNC
    Official Full Name
    expanded repeat domain, CAG/CTG 1provided by HGNC
    Primary source
    HGNC:HGNC:3442
    See related
    MIM:603279
    Gene type
    other
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Annotation information
    not in current annotation release
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    Genomic context

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    Location:
    17q21.3

    Bibliography

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    Related articles in PubMed

    1. A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization. Lee Y, et al. J Biotechnol, 2002 May 23. PMID 12007862
    2. Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders? Lindblad K, et al. Mol Psychiatry, 1998 Sep. PMID 9774773
    3. A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q. Ikeuchi T, et al. Genomics, 1998 Apr 15. PMID 9598323
    4. CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients. Benson KF, et al. Hum Mol Genet, 1998 Oct. PMID 9736780
    5. A CAG/CTG expansion in the normal population. Nakamoto M, et al. Nat Genet, 1997 Dec. PMID 9398837

    See all (6) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Observational study of gene-disease association. (HuGE Navigator)
      Title: European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
    2. Observational study of genetic testing. (HuGE Navigator)
      Title: A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization.
    Submit: New GeneRIF Correction
    Nucleotide Protein
    Heading Accession and Version

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