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    RIEG2 Rieger syndrome 2 [ Homo sapiens (human) ]

    Gene ID: 6012, updated on 2-Oct-2019

    Summary

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    Gene symbol
    RIEG2
    Gene description
    Rieger syndrome 2
    Primary source
    MIM:601499
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    ARS; RGS2

    Genomic context

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    Location:
    13q14

    Bibliography

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    Related articles in PubMed

    1. A human gene encoding a putative basic helix-loop-helix phosphoprotein whose mRNA increases rapidly in cycloheximide-treated blood mononuclear cells. Siderovski DP, et al. DNA Cell Biol, 1994 Feb. PMID 8179820
    2. Differential expression of a basic helix-loop-helix phosphoprotein gene, G0S8, in acute leukemia and localization to human chromosome 1q31. Wu HK, et al. Leukemia, 1995 Aug. PMID 7643615
    3. A set of human putative lymphocyte G0/G1 switch genes includes genes homologous to rodent cytokine and zinc finger protein-encoding genes. Siderovski DP, et al. DNA Cell Biol, 1990 Oct. PMID 1702972
    4. Inhibition of G-protein-mediated MAP kinase activation by a new mammalian gene family. Druey KM, et al. Nature, 1996 Feb 22. PMID 8602223

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Rieger syndrome 2

    General gene information

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    Property

    • phenotype only

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