Details of Epigenetic Molecule(EM)
General Information of EM (ID: EM08238) | |||||||
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Official Symbol |
CEP192
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Official Full Name |
centrosomal protein 192
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Synonym |
FLJ10352;KIAA1569;PPP1R62
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Molecule Type |
Protein coding
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Position On Chromosome |
chr18(Start:12991362 - End:13125052)
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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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2A01: Primary neoplasms of meninges | Meningioma [Primary neoplasms of meninges] | ||||||
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2A90: Mature T-cell lymphoma, specified types, nodal or systemic | Anaplastic large cell lymphoma (ALCL) [Mature T-cell lymphoma, specified types, nodal or systemic] | ||||||
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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 | Colon adenocarcinoma [Malignant neoplasms of colon] | ||||||
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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 adenocarcinoma [Malignant neoplasms of bronchus or lung] | ||||||
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2C25: Malignant neoplasms of bronchus or lung | Lung cancer [Malignant neoplasms of bronchus or lung] | ||||||
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2C30: Melanoma of skin | Cutaneous Melanoma [Melanoma of skin] | ||||||
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2C31: Squamous cell carcinoma of skin | Cutaneous squamous cell carcinoma [Squamous cell carcinoma of skin] | ||||||
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2C60: Carcinoma of breast | Breast cancer [Carcinoma of breast] | ||||||
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2D10: Malignant neoplasms of thyroid gland | Thyroid tumors [Malignant neoplasms of thyroid gland] | ||||||
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4A40: Lupus erythematosus | Systemic lupus erythematosus (SLE) [Lupus erythematosus] | ||||||
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5A02: Thyrotoxicosis | Graves' disease [Thyrotoxicosis] | ||||||
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6A00: Disorders of intellectual development | Intellectual disability and congenital anomalies(ID/CA) [Disorders of intellectual development] | ||||||
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6A02: Autism spectrum disorder | Autism [Autism spectrum disorder] | ||||||
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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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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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DD70: Crohn disease | Crohn's disease [Crohn disease] | ||||||
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EE60: Keloid or hypertrophic scars | Keloid [Keloid or hypertrophic scars] | ||||||
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FA20: Rheumatoid arthritis | Rheumatoid arthritis [Rheumatoid arthritis] | ||||||
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FA21: Psoriatic arthritis | Psoriatic [Psoriatic arthritis] | ||||||
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GA10: Endometriosis | Endometriosis [Endometriosis] | ||||||
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JA24: Pre-eclampsia | Preeclampsia (PE) [Pre-eclampsia] | ||||||
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LA02: Spina bifida | Neural tube defects (NTDs) [Spina bifida] | ||||||
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LD2C: Overgrowth syndromes | Sotos syndrome(SS) [Overgrowth syndromes] | ||||||
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LD2F: Syndromes with multiple structural anomalies, without predominant body system involvement | Silver russell syndrome [Syndromes with multiple structural anomalies, without predominant body system involvement] | ||||||
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LD44: Deletions of the autosomes | Deletion or duplication of chromosome 7q11.23 [Deletions of the autosomes] | ||||||
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MG30: Chronic pain | Fibromyalgia [Chronic pain] | ||||||
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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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XH1ND9: Papillary carcinoma of thyroid | Papillary thyroid carcinoma [Papillary carcinoma of thyroid] | ||||||
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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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XH4V32: Ductal carcinoma in situ | Ductal carcinoma in situ (DCIS) [Ductal carcinoma in situ] | ||||||
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XH7F82: Glioblastoma | Glioblastoma [Glioblastoma] | ||||||
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XH8AA5: Acute myeloid leukaemia | Acute myeloid leukemia (AML) [Acute myeloid leukaemia] | ||||||
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XH8P29: Medulloblastoma | Medulloblastoma [Medulloblastoma] | ||||||
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XH94U0: Pituitary adenoma | Nonfunctioning pituitary adenomas [Pituitary adenoma] | ||||||
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XH98Z3: Schwannoma | Schwannoma [Schwannoma] | ||||||
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XH9HQ1: Gastrointestinal stromal tumour | Gastrointestinal stromal tumors (GIST) [Gastrointestinal stromal tumour] | ||||||
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XN487: Human immunodeficiency virus | Human immunodeficiency virus (HIV) [Human immunodeficiency virus] | ||||||
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Metabolite(s) with this epigenetic modification | |||||||
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Metabolite Name: Valerate | |||||||
Detailed Information |
Meta Info
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[1], [2] | |||||
Description |
Valerate has been shown to hypomethylateCEP192 CpG site in breast cancer cells.
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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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[3] | |||||
Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host CEP192 (geneBody) genetic loci during Mycobacterium tuberculosis H37Rv infection.
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Protein Name: Rv2966c | |||||||
Detailed Information |
Pro Info
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[3] | |||||
Description |
Rv2966c could hypermethylate the non-CpG dinucleotides at the host CEP192 (intergenic) genetic loci during Mycobacterium tuberculosis H37Rv infection.
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