Details of Epigenetic Molecule(EM)
General Information of EM (ID: EM00758) | |||||||
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Official Symbol |
ZBTB37
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Official Full Name |
zinc finger and BTB domain containing 37
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Molecule Type |
Protein coding
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Position On Chromosome |
chr1(Start:173868082 - End:173903549)
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Strand |
+
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Uniprot Entry | |||||||
ENSG ID | |||||||
Dnmivd Disease | |||||||
Disease Relevance (Click to Show/Hide) | |||||||
2B70: Malignant neoplasms of oesophagus | Esophageal adenocarcinoma (EAC) [Malignant neoplasms of oesophagus] | ||||||
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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 | 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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2C73: Malignant neoplasms of ovary | Ovarian serous adenocarcinoma (OSA) [Malignant neoplasms of ovary] | ||||||
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4A40: Lupus erythematosus | Systemic lupus erythematosus (SLE) [Lupus erythematosus] | ||||||
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5A61: Hypofunction or certain specified disorders of pituitary gland | Congenital hypopituitarism [Hypofunction or certain specified disorders of pituitary gland] | ||||||
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5B81: Obesity | Obesity [Obesity] | ||||||
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6A00: Disorders of intellectual development | Intellectual disability and congenital anomalies(ID/CA) [Disorders of intellectual development] | ||||||
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8A00: Parkinsonism | Parkinson's disease (PD) [Parkinsonism] | ||||||
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8A20: Alzheimer disease | Alzheimer's disease [Alzheimer disease] | ||||||
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8A40: Multiple sclerosis | Multiple sclerosis [Multiple sclerosis] | ||||||
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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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DD71: Ulcerative colitis | Ulcerative colitis [Ulcerative colitis] | ||||||
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FA0Z: Osteoarthritis | Osteoarthritis (OA) [Osteoarthritis] | ||||||
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GA10: Endometriosis | Endometriosis [Endometriosis] | ||||||
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LA02: Spina bifida | Neural tube defects (NTDs) [Spina bifida] | ||||||
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LD40: Complete trisomies of the autosomes | Down syndrome (DS) [Complete trisomies of the autosomes] | ||||||
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SE30: Developmental delay disorder | CHARGE and Kabuki syndromes [Developmental delay disorder] | ||||||
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XH1E13: Germinoma | Germinoma [Germinoma] | ||||||
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XH1XF3: Osteosarcoma | Osteosarcoma [Osteosarcoma] | ||||||
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XH4S92: Leukaemia | Leukemia [Leukaemia] | ||||||
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XH4W48: Hepatocellular carcinoma | Hepatocellular carcinoma (HCC) [Hepatocellular carcinoma] | ||||||
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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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XH8P29: Medulloblastoma | Primary medulloblastoma [Medulloblastoma] | ||||||
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XH8P29: Medulloblastoma | Medulloblastoma [Medulloblastoma] | ||||||
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XH8SH6: CNS embryonal tumour | Primitive neuroectodermal tumors [CNS embryonal tumour] | ||||||
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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 ZBTB37 (geneBody) 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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