Details of Epigenetic Molecule(EM)
| General Information of EM (ID: EM12012) | |||||||
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| Official Symbol |
CYP4F22
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| Official Full Name |
Cytochrome P450 Family 4 Subfamily F Member 22
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| Synonym |
Cytochrome P450 Family 4 Subfamily F Member 22;Cytochrome P450, Family 4, Subfamily F, Polypeptide 22;Ultra-Long-Chain Fatty Acid Omega-Hydroxylase;Cytochrome P450 4F22;FLJ39501;INLNE;LI3;EC 1.14.14.177;Cytochrome P450, Family 2, Subfamily E, Polypeptide 2 Homolog
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| Molecule Type |
Protein coding
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| Position On Chromosome |
chr19(Start:15508487 - End:15552317)
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| Strand |
+
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| Uniprot Entry | |||||||
| ENSG ID | |||||||
| Disease Relevance (Click to Show/Hide) | |||||||
| 2C30: Melanoma of skin | Cutaneous Melanoma [Melanoma of skin] | ||||||
| Detailed Information |
Disease Link
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| 8A01: Choreiform disorders | Huntington's disease (HD) [Choreiform disorders] | ||||||
| Detailed Information |
Disease Link
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| 8A20: Alzheimer disease | Alzheimer's disease [Alzheimer disease] | ||||||
| Detailed Information |
Disease Link
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| CB03: Idiopathic interstitial pneumonitis | Idiopathic pulmonary fibrosis (IPF) [Idiopathic interstitial pneumonitis] | ||||||
| Detailed Information |
Disease Link
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| LD2C: Overgrowth syndromes | Sotos syndrome(SS) [Overgrowth syndromes] | ||||||
| Detailed Information |
Disease Link
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| SE30: Developmental delay disorder | CHARGE and Kabuki syndromes [Developmental delay disorder] | ||||||
| Detailed Information |
Disease Link
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| XH4XG8: Chronic myeloid leukaemia | Chronic Phase-Chronic Myeloid Leukemia [Chronic myeloid leukaemia] | ||||||
| Detailed Information |
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| Metabolite(s) with this epigenetic modification | |||||||
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| Metabolite Name: S-Adenosyl Methionine (SAM) | |||||||
| Detailed Information |
Meta Info
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[1], [2] | |||||
| Description |
S-Adenosylmethionine was proved to be decrease CYP4F22 methylation in HT-29 cells.(P value = 0.033)
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