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

Gene ID: 9030, updated on 28-Oct-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; AllianceGenome:HGNC:3442
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
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