Details of Epigenetic Molecule(EM)
General Information of EM (ID: EM09258) | |||||||
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Official Symbol |
USP26
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Official Full Name |
ubiquitin specific peptidase 26
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Molecule Type |
Protein coding
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Position On Chromosome |
chrX(Start:133024631 - End:133097109)
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Strand |
-
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Uniprot Entry | |||||||
ENSG ID | |||||||
Dnmivd Disease | |||||||
Disease Relevance (Click to Show/Hide) | |||||||
2A00: Primary neoplasms of brain | Glioma [Primary neoplasms of brain] | ||||||
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2B70: Malignant neoplasms of oesophagus | Barrett's esophagus and esophageal adenocarcinoma [Malignant neoplasms of oesophagus] | ||||||
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2B72: Malignant neoplasms of stomach | Gastric cancer [Malignant neoplasms of stomach] | ||||||
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2B90: Malignant neoplasms of colon | Colorectal cancer [Malignant neoplasms of colon] | ||||||
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2C25: Malignant neoplasms of bronchus or lung | Lung cancer [Malignant neoplasms of bronchus or lung] | ||||||
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2C25: Malignant neoplasms of bronchus or lung | Non small cell lung cancer (NSCLC) [Malignant neoplasms of bronchus or lung] | ||||||
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2C30: Melanoma of skin | Cutaneous Melanoma [Melanoma of skin] | ||||||
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2C60: Carcinoma of breast | Breast cancer [Carcinoma of breast] | ||||||
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4A40: Lupus erythematosus | Systemic lupus erythematosus (SLE) [Lupus erythematosus] | ||||||
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6A00: Disorders of intellectual development | Intellectual disability and congenital anomalies(ID/CA) [Disorders of intellectual development] | ||||||
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6A20: Schizophrenia | Schizophrenia [Schizophrenia] | ||||||
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9A01: Infectious disorders of eyelid | Human eye and its diseases [Infectious disorders of eyelid] | ||||||
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CA22: Chronic obstructive pulmonary disease | Chronic obstructive pulmonary disease (COPD) [Chronic obstructive pulmonary disease] | ||||||
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DD70: Crohn disease | Crohn's disease [Crohn disease] | ||||||
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LD40: Complete trisomies of the autosomes | Down syndrome (DS) [Complete trisomies of the autosomes] | ||||||
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XB1Y: Familial | Familial recurrent moles (RHM) [Familial] | ||||||
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XH1E13: Germinoma | Germinoma [Germinoma] | ||||||
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XH1XF3: Osteosarcoma | Osteosarcoma [Osteosarcoma] | ||||||
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XH3DV3: Adenoma | Adenoma [Adenoma] | ||||||
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XH4KH2: Adrenal cortical carcinoma | Adrenal cortical cancer [Adrenal cortical carcinoma] | ||||||
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XH4W48: Hepatocellular carcinoma | Hepatocellular carcinoma (HCC) [Hepatocellular carcinoma] | ||||||
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XH68V1: Liver cell adenoma | Hepatocellular adenoma [Liver cell adenoma] | ||||||
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XH7PW5: Lymphocytic leukaemia | Pediatric acute lymphoblastic leukemia [Lymphocytic leukaemia] | ||||||
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XH7ZQ4: Atypical teratoid/rhabdoid tumour | Atypical teratoid/rhabdoid tumor (ATRT) [Atypical teratoid/rhabdoid tumour] | ||||||
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XH8D74: Carcinomatosis | Cancer [Carcinomatosis] | ||||||
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XH8P29: Medulloblastoma | Medulloblastoma [Medulloblastoma] | ||||||
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ZERO(Not Found): Sex chromosome anomalies | X-chromosome inactivation (XCI) [Sex chromosome anomalies] | ||||||
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Protein(s) with this epigenetic modification | |||||||
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Protein Name: Rv2966c | |||||||
Detailed Information |
Pro Info
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[1] | |||||
Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host USP26 (TSS) genetic loci during Mycobacterium tuberculosis H37Rv infection.
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References | |||||
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1 | Genome-wide non-CpG methylation of the host genome during M. tuberculosis infection. Sci Rep. 2016 Apr 26;6:25006. doi: 10.1038/srep25006. |
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