C20orf194

Summary

Gene Symbol: C20orf194
Description: chromosome 20 open reading frame 194
Alias: uncharacterized protein C20orf194
Species: human

Top Publications

  1. pmc Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients
    Alexander J Thompson
    Duke Clinical Research Institute, Duke University Medical Center, Durham, NC 27701, USA
    J Hepatol 56:313-9. 2012
  2. ncbi A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20
    S C Fossey
    Department of Biochemistry, Wake Forest University School of Medicine, Winston Salem, North Carolina, 27157, USA
    Genomics 76:45-57. 2001
  3. pmc Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement
    Hatasu Kobayashi
    Department of Health and Environmental Sciences, Graduate School of Medicine, Kyoto University, Japan
    Am J Hum Genet 89:121-30. 2011

Detail Information

Publications3

  1. pmc Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients
    Alexander J Thompson
    Duke Clinical Research Institute, Duke University Medical Center, Durham, NC 27701, USA
    J Hepatol 56:313-9. 2012
    ..We performed a genome wide association study on a well-characterized genotype 1 HCV cohort to identify genetic determinants of peginterferon-α (pegIFN)-related thrombocytopenia, neutropenia, and leukopenia...
  2. ncbi A high-resolution 6.0-megabase transcript map of the type 2 diabetes susceptibility region on human chromosome 20
    S C Fossey
    Department of Biochemistry, Wake Forest University School of Medicine, Winston Salem, North Carolina, 27157, USA
    Genomics 76:45-57. 2001
    ..The combination of the BAC transcript map, YAC-to-BAC scaffold, and reference Human Genome Project sequence provides a powerful integrated resource for future genomic analysis of this region...
  3. pmc Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement
    Hatasu Kobayashi
    Department of Health and Environmental Sciences, Graduate School of Medicine, Kyoto University, Japan
    Am J Hum Genet 89:121-30. 2011
    ..of an intronic GGCCTG hexanucleotide repeat in NOP56 and an unregistered missense variant (Phe265Leu) in C20orf194, but we found no mutations in PDYN and TGM6...