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CYCSP5 Gene Record

  • Summary
  • Interactions
  • Claims
  • CYCSP5 360158

    Alternate Names:

    360158
    CYTOCHROME C, SOMATIC PSEUDOGENE 5
    CYCSP5
    HCP5
    24416
    ENSG00000227735
    PA142672032
    CYCS PSEUDOGENE 5

    Gene Info:

    Gene Biotype PROCESSED_PSEUDOGENE
    (0 More Sources)

    Gene Categories: Category Details

    Publications:

    Cheng L et al., 2018, The minor alleles HCP5 rs3099844 A and PSORS1C1 rs3131003 G are associated with allopurinol-induced severe cutaneous adverse reactions in Han Chinese: a multicentre retrospective case-control clinical study., Br J Dermatol
    Génin E et al., 2011, Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe., Orphanet J Rare Dis
    Ciccacci C et al., 2017, Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility., Eur J Clin Pharmacol
    Borgiani P et al., 2014, HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique., Eur J Clin Pharmacol
  • NEVIRAPINE   CYCSP5

    Interaction Score: 4.03

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    28689274 24322967


    Sources:
    PharmGKB

  • ALLOPURINOL   CYCSP5

    Interaction Score: 3.2

    Interaction Types & Directionality:
    n/a

    Interaction Info:

    PMIDs:
    29193002 21801394


    Sources:
    PharmGKB

  • Ensembl: ENSG00000227735

    • Version: 101_38

    Alternate Names:
    CYCSP5 Ensembl Gene Name

    Gene Info:
    Gene Biotype PROCESSED_PSEUDOGENE

    Publications:

  • PharmGKB: CYCSP5

    • Version: 18-August-2020

    Alternate Names:
    PA142672032 PharmGKB ID

    Gene Info:

    Publications:
    Génin E et al., 2011, Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe., Orphanet J Rare Dis
    Cheng L et al., 2018, The minor alleles HCP5 rs3099844 A and PSORS1C1 rs3131003 G are associated with allopurinol-induced severe cutaneous adverse reactions in Han Chinese: a multicentre retrospective case-control clinical study., Br J Dermatol
    Borgiani P et al., 2014, HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons Syndrome/Toxic Epidermal Necrolysis susceptibility in a population from Mozambique., Eur J Clin Pharmacol

Disclaimer: This resource is intended for purely research purposes. It should not be used for emergencies or medical or professional advice.

A finding of a drug-gene interaction or potentially druggable category does not necessarily indicate effectiveness (or lack thereof) of any drug or treatment regimen. A finding of no interaction or no potentially druggable category does not necessarily indicate lack of effectiveness of any drug or treatment regimen. Drug-gene interactions or potentially druggable categories are not presented in ranked order of potential or predicted efficacy.

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DGIdb (v4.2.0 - sha1 afd9f30b) • Last updated 2020-10-21