Details of Epigenetic Molecule(EM)
General Information of EM (ID: EM09271) | |||||||
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Official Symbol |
CXorf66
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Official Full Name |
chromosome X open reading frame 66
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Synonym |
RP11-35F15.2
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Molecule Type |
Protein coding
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Position On Chromosome |
chrX(Start:139955725 - End:139965520)
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Strand |
-
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Uniprot Entry | |||||||
ENSG ID | |||||||
Disease Relevance (Click to Show/Hide) | |||||||
2A00: Primary neoplasms of brain | Glioma [Primary neoplasms of brain] | ||||||
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2B6B: Malignant neoplasms of nasopharynx | Nasopharyngeal carcinoma (NPC) [Malignant neoplasms of nasopharynx] | ||||||
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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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4A40: Lupus erythematosus | Systemic lupus erythematosus (SLE) [Lupus erythematosus] | ||||||
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6A20: Schizophrenia | Schizophrenia [Schizophrenia] | ||||||
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6E8Z: Mental, behavioural or neurodevelopmental disorders | Psychiatric disorders [Mental, behavioural or neurodevelopmental disorders] | ||||||
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9A01: Infectious disorders of eyelid | Human eye and its diseases [Infectious disorders of eyelid] | ||||||
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BD40: Atherosclerotic chronic arterial occlusive disease | Atherosclerosis [Atherosclerotic chronic arterial occlusive disease] | ||||||
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CA22: Chronic obstructive pulmonary disease | Chronic obstructive pulmonary disease (COPD) [Chronic obstructive pulmonary disease] | ||||||
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FA20: Rheumatoid arthritis | Rheumatoid arthritis [Rheumatoid arthritis] | ||||||
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JA24: Pre-eclampsia | Preeclampsia (PE) [Pre-eclampsia] | ||||||
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LD2C: Overgrowth syndromes | Sotos syndrome(SS) [Overgrowth syndromes] | ||||||
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SD86: Dementia disorder | Dementia [Dementia disorder] | ||||||
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SE30: Developmental delay disorder | CHARGE and Kabuki syndromes [Developmental delay disorder] | ||||||
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XB8M: Congenital | Melanoma [Congenital] | ||||||
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XH1E13: Germinoma | Germinoma [Germinoma] | ||||||
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XH3DV3: Adenoma | Adenoma [Adenoma] | ||||||
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XH4546: Signet ring cell carcinoma | Signet ring cell colorectal cancer [Signet ring cell carcinoma] | ||||||
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XH4KH2: Adrenal cortical carcinoma | Adrenal cortical cancer [Adrenal cortical carcinoma] | ||||||
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XH6PH6: Astrocytoma | Astrocytoma [Astrocytoma] | ||||||
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XH7PW5: Lymphocytic leukaemia | Pediatric acute lymphoblastic leukemia [Lymphocytic leukaemia] | ||||||
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XH85Z0: Neuroblastoma | Neuroblastoma [Neuroblastoma] | ||||||
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XH8AA5: Acute myeloid leukaemia | Acute myeloid leukemia (AML) [Acute myeloid leukaemia] | ||||||
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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 | |||||||
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Pro Info
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[1] | |||||
Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host CXorf66 (intergenic) 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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