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    ABCC11 ATP binding cassette subfamily C member 11 [ Homo sapiens (human) ]

    Gene ID: 85320, updated on 2-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Functional characterization of variants in human ABCC11, an axillary osmidrosis risk factor.

    Functional characterization of variants in human ABCC11, an axillary osmidrosis risk factor.
    Toyoda Y, Matsuo H, Takada T.

    07/11/2024
    Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo-optico-neuropathy (SMON).

    Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo-optico-neuropathy (SMON).
    Matsumoto H, Sasai H, Kawamoto N, Katsuyama M, Minamiyama M, Kuru S, Fukao T, Ohnishi H, SMON research group members., Free PMC Article

    07/30/2022
    Association of HLA-DPB1, NLRP10, OVOL1, and ABCC11 with the axillary microbiome in a Japanese population.

    Association of HLA-DPB1, NLRP10, OVOL1, and ABCC11 with the axillary microbiome in a Japanese population.
    Kutsuwada Y, Yokota K, Yoshida K, Tsuda H, Watanabe K, Matsumoto A, Iwamoto S.

    03/19/2022
    Association Between Earwax-Determinant Genotypes and Acquired Middle Ear Cholesteatoma in a Japanese Population.

    Association Between Earwax-Determinant Genotypes and Acquired Middle Ear Cholesteatoma in a Japanese Population.
    Hara S, Kusunoki T, Nakagawa H, Toyoda Y, Nojiri S, Kamiya K, Furukawa M, Takata Y, Okada H, Anzai T, Matsumoto F, Ikeda K.

    02/26/2022
    MRP8/14 mediates macrophage efferocytosis through RAGE and Gas6/MFG-E8, and induces polarization via TLR4-dependent pathway.

    MRP8/14 mediates macrophage efferocytosis through RAGE and Gas6/MFG-E8, and induces polarization via TLR4-dependent pathway.
    Li K, Chen G, Luo H, Li J, Liu A, Yang C, Wang J, Xu J, Gao S, Chen P, Jiang Y.

    09/11/2021
    Mutation differences in circulating tumor DNAs from non-small cell lung cancer patients between Uygur and Han populations.

    Mutation differences in circulating tumor DNAs from non-small cell lung cancer patients between Uygur and Han populations.
    Wang Y, Li J, Huang J, Wu C, Li L, Gong P., Free PMC Article

    02/20/2021
    Expression of ATP-binding Cassette Transporter 11 (ABCC11) Protein in Colon Cancer.

    Expression of ATP-binding Cassette Transporter 11 (ABCC11) Protein in Colon Cancer.
    Yamada Y, Yoshimatsu K, Yokomizo H, Okayama S, Shiozawa S.

    10/10/2020
    Rs17822931, a functional single nucleotide polymorphism (SNP) in ABCC11, may play a role in the carcinogenesis.

    A functional single nucleotide polymorphism in ABCC11, rs17822931, is associated with the risk of breast cancer in Japanese.
    Ishiguro J, Ito H, Tsukamoto M, Iwata H, Nakagawa H, Matsuo K.

    02/22/2020
    here were significant differences in SNPs at rs1256061 of estrogen receptor beta gene and rs17822931, rs16945916 and rs62058521 in ABCC11 gene between the axillary osmidrosis patients and normal people

    [Correlation between estrogen receptor β and ABCC11 gene single nucleotide polymorphisms and axillary osmidrosis].
    Hu R, Guo Y, Long J.

    04/27/2019
    the differential expression pattern of ABCC11 and ABCB5 genes may serve as outliers, potentially associated with incidence of multifocal/multicentric breast cancer

    Study of differential gene expression between invasive multifocal/ multicentric and unifocal breast cancer.
    Lang Z, Wu Y, Pan X, Qu G, Zhang T.

    02/2/2019
    The previous findings of a previously unreported homozygous genotype for both the Delta27 and A alleles suggest that the Delta27 deletion might have occurred in the A allele of ABCC11 gene with the 538G>A mutation.

    A Novel Association between the 27-bp Deletion and 538G>A Mutation in the ABCC11 Gene.
    Hori YS, Yamada A, Matsuda N, Ono Y, Starenki D, Sosonkina N, Yoshiura KI, Niikawa N, Ohta T.

    12/22/2018
    our study has provided conclusive evidence for the association of rs17822931 in the ABCC11 with the susceptibility of AO in the Chinese Han population

    A missense variant of the ABCC11 gene is associated with Axillary Osmidrosis susceptibility and clinical phenotypes in the Chinese Han Population.
    Ren Y, Liu W, Chen J, Wang J, Wang K, Zhou J, Cai S, Zheng M, Liu J, Liu L, Xue D., Free PMC Article

    12/1/2018
    Serum levels of MRP8/MRP14 and MRP6 were up-regulated in patients with Graves' disease (GD) and Hashimoto's thyroiditis (HT). In addition, mRNA expression of MRP proteins in PBMCs and the thyroid gland was markedly elevated in these patients.

    Myeloid related proteins are up-regulated in autoimmune thyroid diseases and activate toll-like receptor 4 and pro-inflammatory cytokines in vitro.
    Peng S, Sun X, Wang X, Wang H, Shan Z, Teng W, Li C.

    10/13/2018
    High MRP8 expression is associated with Rheumatoid Arthritis.

    Clinical Significance of Myeloid-Related Protein 8/14 as a Predictor for Biological Treatment and Disease Activity in Rheumatoid Arthritis.
    Yunchun L, Yue W, Jun FZ, Qizhu S, Liumei D.

    09/22/2018
    ABCC11 c.1637C>T polymorphisms affects fluoropyrimidine toxicity to leukocytes

    The impact of ABCC11 polymorphisms on the risk of early-onset fluoropyrimidine toxicity.
    Hamzic S, Wenger N, Froehlich TK, Joerger M, Aebi S, Largiadèr CR, Amstutz U.

    04/21/2018
    Our results confirmed the association between NAF yield and earwax phenotype through ABCC11 genotype. Combined with the recency of last birth, ABCC11 genotype should be considered in the design of studies utilizing NAF as a biosample.

    Genetic Determinants of Nipple Aspiration Fluid Yield.
    Shidfar A, Wang J, Wiesenfeld E, Zhang W, Scholtens D, Fought A, Chatterton RT, Khan SA.

    01/27/2018
    Tenofovir disoproxil fumarate is a new substrate of ABCC11.

    Tenofovir Disoproxil Fumarate Is a New Substrate of ATP-Binding Cassette Subfamily C Member 11.
    Tun-Yhong W, Chinpaisal C, Pamonsinlapatham P, Kaewkitichai S., Free PMC Article

    09/23/2017
    These results suggest that N-linked glycosylation is important for the protein stability of ABCC11, and physiological alteration in glucose may affect the ABCC11 protein level and ABCC11-related phenotypes in humans, such as axillary osmidrosis.

    Regulation of the Axillary Osmidrosis-Associated ABCC11 Protein Stability by N-Linked Glycosylation: Effect of Glucose Condition.
    Toyoda Y, Takada T, Miyata H, Ishikawa T, Suzuki H., Free PMC Article

    07/15/2017
    The present study shows that the protein expression of ABCC10 significantly associates with overall survival and the expression of ABCC11 with disease-free interval of colorectal cancer patients

    Protein expression of ATP-binding cassette transporters ABCC10 and ABCC11 associates with survival of colorectal cancer patients.
    Krizkova V, Dubova M, Susova S, Vycital O, Bruha J, Skala M, Liska V, Daum O, Soucek P.

    06/10/2017
    ABCC11 protein was detected in the human axillary apocrine glands of the 538GG homozygote or 538GA heterozygote, not in the 538AA homozygote. These findings would contribute to a better understanding of the molecular basis of axillary osmidrosis.

    Clinical and Molecular Evidence of ABCC11 Protein Expression in Axillary Apocrine Glands of Patients with Axillary Osmidrosis.
    Toyoda Y, Takada T, Gomi T, Nakagawa H, Ishikawa T, Suzuki H., Free PMC Article

    04/29/2017
    No Association of the rs17822931 Polymorphism in ABCC11 was found with Breast Cancer Risk in Koreans.

    No Association of the rs17822931 Polymorphism in ABCC11 with Breast Cancer Risk in Koreans.
    Na AY, Heo JC, Sung JY, Lee JH, Kim YN, Kim DK.

    02/4/2017
    Presents a simple isothermal genotyping method capable of detecting single nucleotide polymorphisms in the human ATP-binding cassette transporter ABCC11 gene and its application to the clinical diagnosis of axillary osmidrosis.

    Diagnosis of Human Axillary Osmidrosis by Genotyping of the Human ABCC11 Gene: Clinical Practice and Basic Scientific Evidence.
    Toyoda Y, Gomi T, Nakagawa H, Nagakura M, Ishikawa T., Free PMC Article

    01/14/2017
    identified c.1637C>T (T546M), previously associated with 5-FU-related toxicity, as a novel functionally damaging ABCC11 variant exhibiting markedly reduced transport function of 5-FdUMP, the active cytotoxic metabolite of 5-FU. Detailed analysis of 14 subpopulations revealed highest allele frequencies of c.1637C>T in Europeans and Americans (up to 11%) compared with Africans and Asians (up to 3%).

    Functional characterization of common protein variants in the efflux transporter ABCC11 and identification of T546M as functionally damaging variant.
    Arlanov R, Lang T, Jedlitschky G, Schaeffeler E, Ishikawa T, Schwab M, Nies AT.

    10/8/2016
    The ABCC11 gene SNP of the 538 G>A allele was associated with a downregulation of the mRNA expression of ApoD in the apocrine glands, which may indicate a role for the ABCC11 gene in the mediation of osmidrosis

    Association between the ABCC11 gene polymorphism and the expression of apolipoprotein D by the apocrine glands in axillary osmidrosis.
    Zhu Z, Zhang H, Luo G, Xu N, Pan Z.

    12/5/2015
    A single nucleotide polymorphism in ABCC11 affects the cerumen volatile organic compounds profiles of individuals from African, Caucasian, and Asian descent.

    Ethnic/racial and genetic influences on cerumen odorant profiles.
    Prokop-Prigge KA, Mansfield CJ, Parker MR, Thaler E, Grice EA, Wysocki CJ, Preti G., Free PMC Article

    09/26/2015
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