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![]() | Differntial gene expression between RNA A-to-I edited tumor samples versus normal samples |
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![]() | The effects of the RNA editing to the stability of the RNA structures |
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Editing gene: MFSD2A (CAeditome ID:84879) |
Gene summary for MFSD2A |
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Gene information | Gene symbol | MFSD2A | Gene ID | 84879 |
Gene name | major facilitator superfamily domain containing 2A | |
Synonyms | MCPH15|MFSD2|NEDMISBA|NLS1|SLC59A1 | |
Cytomap | 1p34.2 | |
Type of gene | protein-coding | |
Description | sodium-dependent lysophosphatidylcholine symporter 1major facilitator superfamily domain-containing protein 2Asodium-dependent LPC symporter 1 | |
Modification date | 20210518 | |
UniProtAcc | Q8NA29 | |
Context | - 30292405(MFSD2A expression predicts better prognosis in gastric cancer) |
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Gene | GO ID | GO term | PubMed ID |
MFSD2A | GO:0051978 | Sodium-dependent lysophosphatidylcholine symporter 1 | 24828044 |
MFSD2A | GO:0051977 | Sodium-dependent lysophosphatidylcholine symporter 1 | 24828044 |
MFSD2A | GO:0005886 | Sodium-dependent lysophosphatidylcholine symporter 1 | 26005865 |
MFSD2A | GO:0005886 | Sodium-dependent lysophosphatidylcholine symporter 1 | 26005868 |
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RNA A-to-I events for MFSD2A |
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CAediting_50244(39956782, +), CAediting_50245(39956795, +), CAediting_50246(39959442, +), CAediting_50247(39959723, +), CAediting_50248(39959729, +), CAediting_50249(39959737, +), CAediting_50250(39959772, +), CAediting_50251(39959775, +), CAediting_50252(39959777, +), CAediting_50253(39959778, +), CAediting_50254(39959780, +), CAediting_50255(39959784, +), CAediting_50256(39959799, +), CAediting_50257(39959802, +), CAediting_50258(39959803, +), CAediting_50259(39959818, +), CAediting_50260(39959828, +), CAediting_50261(39959833, +), CAediting_50262(39959859, +), CAediting_50263(39959862, +), CAediting_50264(39959880, +), CAediting_50265(39960180, +), CAediting_50266(39961523, +), CAediting_50267(39961559, +), CAediting_50268(39961909, +), CAediting_50269(39961933, +), CAediting_50270(39961938, +), CAediting_50271(39961950, +), CAediting_50272(39961974, +), CAediting_50273(39962010, +), CAediting_50274(39962018, +), CAediting_50275(39962021, +), CAediting_50276(39962026, +), CAediting_50277(39962038, +), CAediting_50278(39962040, +), CAediting_50279(39962057, +), CAediting_50280(39962068, +), CAediting_50281(39962075, +), CAediting_50282(39962076, +), CAediting_50283(39962080, +), CAediting_50284(39963759, +), |
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RNA editing positional annotations for MFSD2A using Annovar |
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CAeditome ID | Position | Variant type | ENST | NTchange | AAchange | SIFT_score | Polyphen2_HVAR_score | PROVEAN_pred |
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CAeditome ID | Position | Variant type |
CAediting_50244 | chr1_39956782_+ | ncRNA_intronic |
CAediting_50245 | chr1_39956795_+ | ncRNA_intronic |
CAediting_50246 | chr1_39959442_+ | ncRNA_intronic |
CAediting_50247 | chr1_39959723_+ | ncRNA_intronic |
CAediting_50248 | chr1_39959729_+ | ncRNA_intronic |
CAediting_50249 | chr1_39959737_+ | ncRNA_intronic |
CAediting_50250 | chr1_39959772_+ | ncRNA_intronic |
CAediting_50251 | chr1_39959775_+ | ncRNA_intronic |
CAediting_50252 | chr1_39959777_+ | ncRNA_intronic |
CAediting_50253 | chr1_39959778_+ | ncRNA_intronic |
CAediting_50254 | chr1_39959780_+ | ncRNA_intronic |
CAediting_50255 | chr1_39959784_+ | ncRNA_intronic |
CAediting_50256 | chr1_39959799_+ | ncRNA_intronic |
CAediting_50257 | chr1_39959802_+ | ncRNA_intronic |
CAediting_50258 | chr1_39959803_+ | ncRNA_intronic |
CAediting_50259 | chr1_39959818_+ | ncRNA_intronic |
CAediting_50260 | chr1_39959828_+ | ncRNA_intronic |
CAediting_50261 | chr1_39959833_+ | ncRNA_intronic |
CAediting_50262 | chr1_39959859_+ | ncRNA_intronic |
CAediting_50263 | chr1_39959862_+ | ncRNA_intronic |
CAediting_50264 | chr1_39959880_+ | ncRNA_intronic |
CAediting_50265 | chr1_39960180_+ | ncRNA_intronic |
CAediting_50266 | chr1_39961523_+ | ncRNA_intronic |
CAediting_50267 | chr1_39961559_+ | ncRNA_intronic |
CAediting_50268 | chr1_39961909_+ | ncRNA_intronic |
CAediting_50269 | chr1_39961933_+ | ncRNA_intronic |
CAediting_50270 | chr1_39961938_+ | ncRNA_intronic |
CAediting_50271 | chr1_39961950_+ | ncRNA_intronic |
CAediting_50272 | chr1_39961974_+ | ncRNA_intronic |
CAediting_50273 | chr1_39962010_+ | ncRNA_intronic |
CAediting_50274 | chr1_39962018_+ | ncRNA_intronic |
CAediting_50275 | chr1_39962021_+ | ncRNA_intronic |
CAediting_50276 | chr1_39962026_+ | ncRNA_intronic |
CAediting_50277 | chr1_39962038_+ | ncRNA_intronic |
CAediting_50278 | chr1_39962040_+ | ncRNA_intronic |
CAediting_50279 | chr1_39962057_+ | ncRNA_intronic |
CAediting_50280 | chr1_39962068_+ | ncRNA_intronic |
CAediting_50281 | chr1_39962075_+ | ncRNA_intronic |
CAediting_50282 | chr1_39962076_+ | ncRNA_intronic |
CAediting_50283 | chr1_39962080_+ | ncRNA_intronic |
CAediting_50284 | chr1_39963759_+ | ncRNA_intronic |
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CAeditome ID | Position | Repeat family | Repeat sub family | Repeat name |
CAediting_50244 | chr1_39956782_+ | SINE | Alu | AluY |
CAediting_50245 | chr1_39956795_+ | SINE | Alu | AluY |
CAediting_50246 | chr1_39959442_+ | SINE | Alu | AluJr |
CAediting_50247 | chr1_39959723_+ | SINE | MIR | MIRb |
CAediting_50248 | chr1_39959729_+ | SINE | MIR | MIRb |
CAediting_50249 | chr1_39959737_+ | SINE | MIR | MIRb |
CAediting_50250 | chr1_39959772_+ | SINE | MIR | MIRb |
CAediting_50251 | chr1_39959775_+ | SINE | MIR | MIRb |
CAediting_50252 | chr1_39959777_+ | SINE | MIR | MIRb |
CAediting_50253 | chr1_39959778_+ | SINE | MIR | MIRb |
CAediting_50254 | chr1_39959780_+ | SINE | MIR | MIRb |
CAediting_50255 | chr1_39959784_+ | SINE | MIR | MIRb |
CAediting_50256 | chr1_39959799_+ | SINE | MIR | MIRb |
CAediting_50257 | chr1_39959802_+ | SINE | MIR | MIRb |
CAediting_50258 | chr1_39959803_+ | SINE | MIR | MIRb |
CAediting_50266 | chr1_39961523_+ | SINE | Alu | AluY |
CAediting_50267 | chr1_39961559_+ | SINE | Alu | AluY |
CAediting_50284 | chr1_39963759_+ | SINE | Alu | AluSx |
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RNA A-to-I editing events in the alternative splicing sites for MFSD2A |
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AStype | CAeditomID | Editing position | AS position | AS direction | Exonic location | Wildtype sequence | Wildtype splicing strength | RNA edited sequence | RNA edited splicing strength |
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Differntial gene expression between RNA A-to-I edited versus non-edited samples for MFSD2A |
![]() * The grey color means N/A. |
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LUAD.CAediting_50249.ENSG00000168389.MFSD2A.png ![]() |
LUAD.CAediting_50257.ENSG00000168389.MFSD2A.png ![]() |
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Protein coding region RNA A-to-I editings for MFSD2A |
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The effects of the RNA editing to the miRNA binding sites for MFSD2A |
**If you are searching a miRNA gene with RNA editing events in its seed regions, please see the search pages of miRNA targets to discover the effects of this RNA editing event to miRNA regulations. For more information, please check the files in the Download page. |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
CAediting_524911 | chr7_5495852_- | ENSG00000168389.16 | ENST00000420632 | hsa-miR-589-3p | 39969727 | 39969733 | 7mer-m8 | 39969713 | 39969734 | 161 | -35.48 |
CAediting_524911 | chr7_5495852_- | ENSG00000168389.16 | ENST00000372809 | hsa-miR-589-3p | 39969727 | 39969733 | 7mer-m8 | 39969713 | 39969734 | 161 | -35.48 |
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CAeditom_ID | Position | ENSG | ENST | miRNA | Targetscan start | Targetscan end | Targetscan score | Miranda start | Miranda end | Miranda score | Miranda energy |
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The effects of the RNA editing to the stability of the RNA structures for MFSD2A |
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ENST | ENST type | RNA structure without RNA A-to-I editing. | RNA structure with RNA A-to-I editing. |
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CAeditom_ID | ENST | Editing_Position | MFE_withoneAI | MFE_withoutAI | MFE_withmultipleAI |
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Relation with ADAR for MFSD2A |
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Cancer | CAeditomID | position | ADAR1 (p-val) | ADAR1 (coeff.) | ADAR2 (p-val) | ADAR2 (coeff.) | ADAR3 (p-val) | ADAR3 (coeff.) |
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Relation with cancer stages for MFSD2A |
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Cancer | Stage_type | CAeditomID | position | P-val | Coeff. |
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Relation with survival for MFSD2A |
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Cancer | CAeditomID | position | KMpvalue | Coxpvalue | CoxHR |
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RelatedDrugs for MFSD2A |
![]() (DrugBank Version 5.1.8 2021-01-03) |
Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for MFSD2A |
![]() (DisGeNet 7.0) |
Gene | Disease ID | Disease name | # pubmeds | Source |
MFSD2A | C4225310 | MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE | 3 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
MFSD2A | C0025958 | Microcephaly | 2 | CTD_human |
MFSD2A | C1956147 | Microlissencephaly | 2 | CTD_human |
MFSD2A | C3711387 | Autosomal Recessive Primary Microcephaly | 2 | ORPHANET |
MFSD2A | C3853041 | Severe Congenital Microcephaly | 2 | CTD_human |
MFSD2A | C0009090 | Cluttering | 1 | CTD_human |
MFSD2A | C0020796 | Profound Mental Retardation | 1 | CTD_human |
MFSD2A | C0025363 | Mental Retardation, Psychosocial | 1 | CTD_human |
MFSD2A | C0037822 | Speech Disorders | 1 | CTD_human |
MFSD2A | C0233726 | Aprosodia | 1 | CTD_human |
MFSD2A | C0751512 | Dysglossia | 1 | CTD_human |
MFSD2A | C0751513 | Rhinolalia | 1 | CTD_human |
MFSD2A | C0751514 | Verbal Fluency Disorders | 1 | CTD_human |
MFSD2A | C0917816 | Mental deficiency | 1 | CTD_human |
MFSD2A | C2239176 | Liver carcinoma | 1 | CTD_human |
MFSD2A | C3495145 | Dyslalia | 1 | CTD_human |
MFSD2A | C3714756 | Intellectual Disability | 1 | CTD_human |