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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: FLNA (CAeditome ID:2316) |
Gene summary for FLNA |
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Gene information | Gene symbol | FLNA | Gene ID | 2316 |
Gene name | filamin A | |
Synonyms | ABP-280|ABPX|CSBS|CVD1|FGS2|FLN|FLN-A|FLN1|FMD|MNS|NHBP|OPD|OPD1|OPD2|XLVD|XMVD | |
Cytomap | Xq28 | |
Type of gene | protein-coding | |
Description | filamin-Aactin binding protein 280alpha-filaminendothelial actin-binding proteinepididymis secretory sperm binding proteinfilamin A, alphafilamin-1non-muscle filamin | |
Modification date | 20210518 | |
UniProtAcc | P21333 | |
Context |
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Gene | GO ID | GO term | PubMed ID |
FLNA | GO:0090307 | Filamin-A | 18548008 |
FLNA | GO:0015459 | Filamin-A | 24951510 |
FLNA | GO:0031267 | Filamin-A | 10051605 |
FLNA | GO:0034988 | Filamin-A | 1833070 |
FLNA | GO:0042803 | Filamin-A | 2391361 |
FLNA | GO:0051015 | Filamin-A | 2391361 |
FLNA | GO:0051015 | Filamin-A | 25358863 |
FLNA | GO:0051015 | Filamin-A | 3138234 |
FLNA | GO:0051015 | Filamin-A | 4044584 |
FLNA | GO:0016479 | Filamin-A | 22307607 |
FLNA | GO:0030334 | Filamin-A | 16291724 |
FLNA | GO:0031532 | Filamin-A | 10051605 |
FLNA | GO:0034394 | Filamin-A | 18322202 |
FLNA | GO:0043113 | Filamin-A | 10692483 |
FLNA | GO:0043433 | Filamin-A | 15684392 |
FLNA | GO:0044319 | Filamin-A | 16291724 |
FLNA | GO:0045184 | Filamin-A | 18322202 |
FLNA | GO:0051764 | Filamin-A | 10051605 |
FLNA | GO:0072659 | Filamin-A | 24951510 |
FLNA | GO:1901381 | Filamin-A | 24951510 |
FLNA | GO:0005634 | Filamin-A | 15684392 |
FLNA | GO:0005737 | Filamin-A | 15684392 |
FLNA | GO:0005737 | Filamin-A | 21914078 |
FLNA | GO:0005737 | Filamin-A | 25468996 |
FLNA | GO:0005829 | Filamin-A | 0000052 |
FLNA | GO:0005886 | Filamin-A | 0000052 |
FLNA | GO:0005886 | Filamin-A | 18322202 |
FLNA | GO:0005911 | Filamin-A | 16291724 |
FLNA | GO:0015629 | Filamin-A | 0000052 |
FLNA | GO:0015629 | Filamin-A | 25358863 |
FLNA | GO:0031523 | Filamin-A | 18548008 |
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RNA A-to-I events for FLNA |
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CAediting_1527831(154351043, -), CAediting_1527832(154351318, -), CAediting_1527833(154351354, -), CAediting_1527834(154351368, -), CAediting_1527835(154351522, -), CAediting_1527836(154351569, -), CAediting_1527837(154363144, -), CAediting_1527838(154363458, -), |
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RNA editing positional annotations for FLNA 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_1527831 | chrX_154351043_- | ncRNA_exonic;splicing |
CAediting_1527832 | chrX_154351318_- | ncRNA_exonic |
CAediting_1527833 | chrX_154351354_- | ncRNA_exonic |
CAediting_1527834 | chrX_154351368_- | ncRNA_exonic |
CAediting_1527835 | chrX_154351522_- | ncRNA_exonic |
CAediting_1527836 | chrX_154351569_- | ncRNA_exonic |
CAediting_1527837 | chrX_154363144_- | intronic |
CAediting_1527838 | chrX_154363458_- | intronic |
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CAeditome ID | Position | Repeat family | Repeat sub family | Repeat name |
CAediting_1527837 | chrX_154363144_- | SINE | Alu | AluSp |
CAediting_1527838 | chrX_154363458_- | SINE | Alu | AluYf1 |
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RNA A-to-I editing events in the alternative splicing sites for FLNA |
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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 |
ES | CAediting_1527831 | chrX_154351043_- | 154351032:154351054 | 3SS | 0+9i | GCTGTGCTTCCAGGAGTCAGGGC | -8.52 | GCTGTGCTTCCGGGAGTCAGGGC | -1.6 |
ES | CAediting_1527831 | chrX_154351043_- | 154351036:154351058 | 3SS | 0+5i | GTCTGCTGTGCTTCCAGGAGTCA | -15.57 | GTCTGCTGTGCTTCCGGGAGTCA | -8.83 |
ES | CAediting_1527831 | chrX_154351043_- | 154351039:154351061 | 3SS | 0+2i | CATGTCTGCTGTGCTTCCAGGAG | 9.12 | CATGTCTGCTGTGCTTCCGGGAG | 1.17 |
IR | CAediting_1527831 | chrX_154351043_- | 154351032:154351054 | 3SS | 0+9i | GCTGTGCTTCCAGGAGTCAGGGC | -8.52 | GCTGTGCTTCCGGGAGTCAGGGC | -1.6 |
IR | CAediting_1527831 | chrX_154351043_- | 154351036:154351058 | 3SS | 0+5i | GTCTGCTGTGCTTCCAGGAGTCA | -15.57 | GTCTGCTGTGCTTCCGGGAGTCA | -8.83 |
IR | CAediting_1527831 | chrX_154351043_- | 154351039:154351061 | 3SS | 0+2i | CATGTCTGCTGTGCTTCCAGGAG | 9.12 | CATGTCTGCTGTGCTTCCGGGAG | 1.17 |
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Differntial gene expression between RNA A-to-I edited versus non-edited samples for FLNA |
![]() * The grey color means N/A. |
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Protein coding region RNA A-to-I editings for FLNA |
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The effects of the RNA editing to the miRNA binding sites for FLNA |
**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_688081 | chr9_63819627_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4477b | 154361741 | 154361747 | 7mer-m8 | 154361740 | 154361757 | 142 | -11.74 |
CAediting_846604 | chr11_93733708_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-1304-3p | 154354200 | 154354206 | 7mer-m8 | 154354199 | 154354223 | 141 | -18.79 |
CAediting_393 | chr1_1167164_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-200b-3p | 154353612 | 154353618 | 7mer-m8 | 154353611 | 154353630 | 143 | -15.54 |
CAediting_86358 | chr1_109598906_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-197-5p | 154364532 | 154364539 | 8mer-1a | 154364532 | 154364553 | 149 | -22.99 |
CAediting_1054808 | chr15_66496985_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4512 | 154364277 | 154364284 | 8mer-1a | 154364277 | 154364301 | 149 | -22.38 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154364090 | 154364096 | 7mer-m8 | 154364089 | 154364109 | 155 | -16.62 |
CAediting_1054808 | chr15_66496985_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4512 | 154362532 | 154362538 | 7mer-m8 | 154362531 | 154362554 | 151 | -26.64 |
CAediting_604450 | chr7_133034877_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-3654 | 154361980 | 154361987 | 8mer-1a | 154361980 | 154361999 | 153 | -19.24 |
CAediting_573000 | chr7_92204081_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-1285-5p | 154362039 | 154362045 | 7mer-m8 | 154362038 | 154362058 | 158 | -21.12 |
CAediting_442554 | chr5_154685830_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-1303 | 154361712 | 154361718 | 7mer-m8 | 154361711 | 154361733 | 145 | -16.92 |
CAediting_1054808 | chr15_66496985_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4512 | 154360474 | 154360479 | 6mer | 154360473 | 154360496 | 143 | -31.49 |
CAediting_1054808 | chr15_66496985_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4512 | 154360291 | 154360297 | 7mer-m8 | 154360290 | 154360311 | 147 | -23.21 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154360410 | 154360416 | 7mer-m8 | 154360409 | 154360432 | 141 | -13.03 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154360070 | 154360077 | 8mer-1a | 154360070 | 154360090 | 140 | -14.15 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154359602 | 154359608 | 7mer-m8 | 154359601 | 154359621 | 140 | -13.3 |
CAediting_580943 | chr7_100356700_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-6840-3p | 154359554 | 154359560 | 7mer-m8 | 154359553 | 154359574 | 142 | -25.33 |
CAediting_524911 | chr7_5495852_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-589-3p | 154359095 | 154359101 | 7mer-m8 | 154359094 | 154359117 | 146 | -17.4 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154358503 | 154358509 | 7mer-m8 | 154358502 | 154358522 | 144 | -12.1 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154357464 | 154357470 | 7mer-m8 | 154357463 | 154357483 | 140 | -14.66 |
CAediting_77128 | chr1_85133844_+ | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4423-3p | 154354844 | 154354851 | 8mer-1a | 154354844 | 154354864 | 140 | -15.39 |
CAediting_573000 | chr7_92204081_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-1285-5p | 154354386 | 154354392 | 7mer-m8 | 154354385 | 154354406 | 154 | -21.12 |
CAediting_1306323 | chr19_13836462_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-27a-3p | 154354223 | 154354229 | 7mer-m8 | 154354222 | 154354242 | 147 | -17.39 |
CAediting_1054808 | chr15_66496985_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-4512 | 154352253 | 154352258 | 6mer | 154352252 | 154352273 | 146 | -21.82 |
CAediting_1399425 | chr20_1392958_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-6869-5p | 154348799 | 154348806 | 8mer-1a | 154348799 | 154348819 | 165 | -28.82 |
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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_604450 | chr7_133034877_- | ENSG00000196924.13 | ENST00000420627 | hsa-miR-3654 | 154362074 | 154362080 | 7mer-m8 | 154362073 | 154362091 | 140 | -17.23 |
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The effects of the RNA editing to the stability of the RNA structures for FLNA |
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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 FLNA |
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Cancer | CAeditomID | position | ADAR1 (p-val) | ADAR1 (coeff.) | ADAR2 (p-val) | ADAR2 (coeff.) | ADAR3 (p-val) | ADAR3 (coeff.) |
PRAD | CAediting_1527831 | chrX_154351043_- | 0.048515167983321 | 0.167660656540094 | . | . | . | . |
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Relation with cancer stages for FLNA |
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Cancer | Stage_type | CAeditomID | position | P-val | Coeff. |
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Relation with survival for FLNA |
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Cancer | CAeditomID | position | KMpvalue | Coxpvalue | CoxHR |
BRCA | CAediting_1527831 | chrX_154351043_- | 0.000370825458820501 | 0.00783027 | 12486200 |
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RelatedDrugs for FLNA |
![]() (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 FLNA |
![]() (DisGeNet 7.0) |
Gene | Disease ID | Disease name | # pubmeds | Source |
FLNA | C1848213 | Periventricular Heterotopia, X-Linked | 9 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
FLNA | C0025237 | Melnick-Needles Syndrome | 7 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
FLNA | C4707243 | Familial thoracic aortic aneurysm and aortic dissection | 7 | CLINGEN;GENOMICS_ENGLAND |
FLNA | C0265251 | Oto-Palato-digital syndrome type 1 | 6 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
FLNA | C1844696 | OTOPALATODIGITAL SYNDROME, TYPE II | 6 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
FLNA | C0265293 | Frontometaphyseal dysplasia | 5 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
FLNA | C1846129 | Terminal Osseous Dysplasia and Pigmentary Defects | 4 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
FLNA | C4281559 | FRONTOMETAPHYSEAL DYSPLASIA 1 | 4 | GENOMICS_ENGLAND;UNIPROT |
FLNA | C0262436 | Cardiac valvular dysplasia, X-linked | 2 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
FLNA | C0543888 | Epileptic encephalopathy | 2 | GENOMICS_ENGLAND |
FLNA | C1845902 | FG SYNDROME 2 | 2 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
FLNA | C1868720 | Periventricular Nodular Heterotopia | 2 | CTD_human |
FLNA | C2746068 | Congenital idiopathic intestinal pseudoobstruction | 2 | CTD_human;GENOMICS_ENGLAND |
FLNA | C4551969 | Bilateral Periventricular Nodular Heterotopia | 2 | CTD_human |
FLNA | C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
FLNA | C0010701 | Phyllodes Tumor | 1 | CTD_human |
FLNA | C0013366 | Dyschondroplasias | 1 | CTD_human |
FLNA | C0014544 | Epilepsy | 1 | CTD_human |
FLNA | C0021847 | Intestinal Pseudo-Obstruction | 1 | ORPHANET |
FLNA | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
FLNA | C0026760 | Multiple Epiphyseal Dysplasia | 1 | CTD_human |
FLNA | C0029422 | Osteochondrodysplasias | 1 | CTD_human |
FLNA | C0036391 | Schwartz-Jampel Syndrome | 1 | CTD_human |
FLNA | C0038015 | Spondyloepiphyseal Dysplasia | 1 | CTD_human |
FLNA | C0086237 | Epilepsy, Cryptogenic | 1 | CTD_human |
FLNA | C0220769 | FG syndrome | 1 | CTD_human |
FLNA | C0236018 | Aura | 1 | CTD_human |
FLNA | C0268341 | Ehlers-Danlos syndrome type 5 | 1 | ORPHANET |
FLNA | C0432272 | Van Buchem disease | 1 | CTD_human |
FLNA | C0600066 | Malignant Cystosarcoma Phyllodes | 1 | CTD_human |
FLNA | C0678222 | Breast Carcinoma | 1 | CTD_human |
FLNA | C0751111 | Awakening Epilepsy | 1 | CTD_human |
FLNA | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
FLNA | C1458155 | Mammary Neoplasms | 1 | CTD_human |
FLNA | C1845235 | Heterotopia, Periventricular, Ehlers-Danlos Variant | 1 | CTD_human |
FLNA | C1845546 | FG SYNDROME 4 (disorder) | 1 | CTD_human |
FLNA | C1845567 | FG SYNDROME 3 | 1 | CTD_human |
FLNA | C1855733 | Neuronal intestinal pseudoobstruction | 1 | ORPHANET |
FLNA | C2751260 | Macrothrombocytopenia | 1 | GENOMICS_ENGLAND |
FLNA | C3541456 | Spondyloepiphyseal Dysplasia Tarda, X-Linked | 1 | CTD_human |
FLNA | C4551479 | Schwartz-Jampel Syndrome, Type 1 | 1 | CTD_human |
FLNA | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |