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International Journal of Oncology
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Print ISSN: 1019-6439 Online ISSN: 1791-2423
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October 2003 Volume 23 Issue 4

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Journals

International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

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Medicine International

An International Open Access Journal Devoted to General Medicine.

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October 2003 Volume 23 Issue 4

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Article

Identification and characterization of TPARM gene in silico

  • Authors:
    • Masuko Katoh
    • Masaru Katoh
  • View Affiliations / Copyright

    Affiliations: M & M Medical BioInformatics, Narashino 275-0022, Japan
  • Pages: 1213-1217
    |
    Published online on: October 1, 2003
       https://doi.org/10.3892/ijo.23.4.1213
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Abstract

Several tumor suppressor genes are located within human chromosome 11q23 region. We have cloned and characterized MFRP and RNF26 genes at 11q23.3. We also identified and characterized KIAA1735/MTHDIX gene at 11q23.1 and CLDN24 gene at 11q23.2 by using bioinformatics. Here, a novel human gene corresponding to a 5'-truncated FLJ20535 cDNA was identified. FLJ20535 corresponded to nucleotide position 55-2255 of FLJ13859, and nucleotide position 52-2169 of FLJ13859 was the coding region. Because of tetratricopeptide repeat (TPR) and armadillo repeat (ARM) domains within its gene product, the novel human gene was designated TPARM. Mouse E330017O07Rik cDNA was derived from mouse Tparm gene. Human TPARM (705 aa) and mouse Tparm (704 aa), showing 75.4% total-amino-acid identity, consist of TPR domain and three ARM domains. TPR domain of TPARM was most homologous to that of SMAP1, while ARM1-ARM3 domains of TPARM were most homologous to ARM7-ARM9 domains of CTNNB1 (also known as β-catenin). TPARM might be implicated in the WNT-β-catenin signaling pathway. TPARM mRNA was expressed in testis, prostate, lung, germinal center B-cells, and also in neuroblastoma, teratocarcinoma, colon cancer, and gastric cancer. Human TPARM gene was found to consist of 22 exons. TPARM gene, located between NCAM1 and DRD2 genes, was mapped to human chromosome 11q23.2. TPARM as well as NCAM1 and DRD2 were predicted to be candidate tumor suppressor genes within the commonly deleted region of malignant melanoma on 11q23.1-q23.2 (between microsatellite markers D11S1347 and D11S4122).

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Copy and paste a formatted citation
Spandidos Publications style
Katoh M and Katoh M: Identification and characterization of TPARM gene in silico. Int J Oncol 23: 1213-1217, 2003.
APA
Katoh, M., & Katoh, M. (2003). Identification and characterization of TPARM gene in silico. International Journal of Oncology, 23, 1213-1217. https://doi.org/10.3892/ijo.23.4.1213
MLA
Katoh, M., Katoh, M."Identification and characterization of TPARM gene in silico". International Journal of Oncology 23.4 (2003): 1213-1217.
Chicago
Katoh, M., Katoh, M."Identification and characterization of TPARM gene in silico". International Journal of Oncology 23, no. 4 (2003): 1213-1217. https://doi.org/10.3892/ijo.23.4.1213
Copy and paste a formatted citation
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Spandidos Publications style
Katoh M and Katoh M: Identification and characterization of TPARM gene in silico. Int J Oncol 23: 1213-1217, 2003.
APA
Katoh, M., & Katoh, M. (2003). Identification and characterization of TPARM gene in silico. International Journal of Oncology, 23, 1213-1217. https://doi.org/10.3892/ijo.23.4.1213
MLA
Katoh, M., Katoh, M."Identification and characterization of TPARM gene in silico". International Journal of Oncology 23.4 (2003): 1213-1217.
Chicago
Katoh, M., Katoh, M."Identification and characterization of TPARM gene in silico". International Journal of Oncology 23, no. 4 (2003): 1213-1217. https://doi.org/10.3892/ijo.23.4.1213
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