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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: ACTG1 (CAeditome ID:71) |
Gene summary for ACTG1 |
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Gene information | Gene symbol | ACTG1 | Gene ID | 71 |
Gene name | actin gamma 1 | |
Synonyms | ACT|ACTG|DFNA20|DFNA26|HEL-176 | |
Cytomap | 17q25.3 | |
Type of gene | protein-coding | |
Description | actin, cytoplasmic 2cytoskeletal gamma-actinepididymis luminal protein 176 | |
Modification date | 20210518 | |
UniProtAcc | P63261 | |
Context |
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Gene | GO ID | GO term | PubMed ID |
ACTG1 | GO:0005522 | Actin, cytoplasmic 2 | 28493397 |
ACTG1 | GO:0005884 | Actin, cytoplasmic 2 | 28493397 |
ACTG1 | GO:0005911 | Actin, cytoplasmic 2 | 22855531 |
ACTG1 | GO:0043296 | Actin, cytoplasmic 2 | 22855531 |
ACTG1 | GO:0070062 | Actin, cytoplasmic 2 | 21557262 |
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RNA A-to-I events for ACTG1 |
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CAediting_1245605(81510432, -), CAediting_1245606(81510558, -), CAediting_1245607(81510587, -), CAediting_1245608(81512085, -), |
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RNA editing positional annotations for ACTG1 using Annovar |
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CAeditome ID | Position | Variant type | ENST | NTchange | AAchange | SIFT_score | Polyphen2_HVAR_score | PROVEAN_pred |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000570382.1 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000571691.4 | c.A154G | p.K52E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000571721.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000572105.5 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000573283.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000575087.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000575659.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000575842.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000575994.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000576544.4 | c.A181G | p.K61E | . | D | N |
CAediting_1245608 | chr17_81512085_- | nonsynonymous SNV | ENST00000615544.3 | c.A181G | p.K61E | . | D | N |
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CAeditome ID | Position | Variant type |
CAediting_1245605 | chr17_81510432_- | ncRNA_exonic |
CAediting_1245606 | chr17_81510558_- | ncRNA_exonic |
CAediting_1245607 | chr17_81510587_- | ncRNA_exonic |
CAediting_1245608 | chr17_81512085_- | exonic |
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CAeditome ID | Position | Repeat family | Repeat sub family | Repeat name |
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RNA A-to-I editing events in the alternative splicing sites for ACTG1 |
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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 |
IR | CAediting_1245605 | chr17_81510432_- | 81510424:81510432 | 5SS | 3+0i | ACGTGTGGC | -13.3 | GCGTGTGGC | -16.38 |
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Differntial gene expression between RNA A-to-I edited versus non-edited samples for ACTG1 |
![]() * The grey color means N/A. |
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Protein coding region RNA A-to-I editings for ACTG1 |
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The effects of the RNA editing to the miRNA binding sites for ACTG1 |
**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 |
CAediting_1245605 | chr17_81510432_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-521 | 81510429 | 81510435 | 7mer-m8 | 81510428 | 81510449 | 140.00 | -11.80 |
CAediting_1245605 | chr17_81510432_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-521 | 81510429 | 81510435 | 7mer-m8 | 81510428 | 81510449 | 140.00 | -11.80 |
CAediting_1245605 | chr17_81510432_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-521 | 81510429 | 81510435 | 7mer-m8 | 81510428 | 81510449 | 140.00 | -11.80 |
CAediting_1245605 | chr17_81510432_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-521 | 81510429 | 81510435 | 7mer-m8 | 81510428 | 81510449 | 140.00 | -11.80 |
CAediting_1245606 | chr17_81510558_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-7109-3p | 81510554 | 81510560 | 7mer-m8 | 81510553 | 81510574 | 140.00 | -15.44 |
CAediting_1245606 | chr17_81510558_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-7109-3p | 81510554 | 81510560 | 7mer-m8 | 81510553 | 81510574 | 140.00 | -15.44 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-3925-3p | 81510587 | 81510593 | 7mer-m8 | 81510586 | 81510605 | 152.00 | -16.79 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-508-5p | 81510585 | 81510592 | 8mer-1a | 81510585 | 81510607 | 140.00 | -16.93 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-550b-3p | 81510583 | 81510589 | 7mer-m8 | 81510582 | 81510601 | 145.00 | -12.59 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-550b-3p | 81510583 | 81510589 | 7mer-m8 | 81510582 | 81510601 | 145.00 | -12.59 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-3925-3p | 81510587 | 81510593 | 7mer-m8 | 81510586 | 81510605 | 152.00 | -16.79 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-508-5p | 81510585 | 81510592 | 8mer-1a | 81510585 | 81510607 | 140.00 | -16.93 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-550b-3p | 81510583 | 81510589 | 7mer-m8 | 81510582 | 81510601 | 145.00 | -12.59 |
CAediting_1245607 | chr17_81510587_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-550b-3p | 81510583 | 81510589 | 7mer-m8 | 81510582 | 81510601 | 145.00 | -12.59 |
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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_980496 | chr14_31014685_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-624-3p | 81510458 | 81510465 | 8mer-1a | 81510458 | 81510480 | 158 | -21.39 |
CAediting_980496 | chr14_31014685_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-624-3p | 81510458 | 81510465 | 8mer-1a | 81510458 | 81510480 | 158 | -21.39 |
CAediting_1054808 | chr15_66496985_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-4512 | 81510018 | 81510025 | 8mer-1a | 81510018 | 81510039 | 152 | -20.1 |
CAediting_1054808 | chr15_66496985_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-4512 | 81510018 | 81510025 | 8mer-1a | 81510018 | 81510039 | 152 | -20.1 |
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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_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-589-3p | 81510300 | 81510306 | 7mer-m8 | 81510299 | 81510323 | 141 | -17.55 |
CAediting_980496 | chr14_31014685_- | ENSG00000184009.8 | ENST00000575842 | hsa-miR-624-3p | 81510501 | 81510508 | 8mer-1a | 81510501 | 81510525 | 145 | -10.16 |
CAediting_524911 | chr7_5495852_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-589-3p | 81510300 | 81510306 | 7mer-m8 | 81510299 | 81510323 | 141 | -17.55 |
CAediting_980496 | chr14_31014685_- | ENSG00000184009.8 | ENST00000575087 | hsa-miR-624-3p | 81510501 | 81510508 | 8mer-1a | 81510501 | 81510525 | 145 | -10.16 |
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The effects of the RNA editing to the stability of the RNA structures for ACTG1 |
![]() * Click on the image to enlarge it in a new window. |
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 ACTG1 |
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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 ACTG1 |
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Cancer | Stage_type | CAeditomID | position | P-val | Coeff. |
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Relation with survival for ACTG1 |
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Cancer | CAeditomID | position | KMpvalue | Coxpvalue | CoxHR |
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RelatedDrugs for ACTG1 |
![]() (DrugBank Version 5.1.8 2021-01-03) |
Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
ACTG1 | P63261 | DB09130 | Copper | Actin, cytoplasmic 2 | SmallMoleculeDrug | approved|investigational |
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RelatedDiseases for ACTG1 |
![]() (DisGeNet 7.0) |
Gene | Disease ID | Disease name | # pubmeds | Source |
ACTG1 | C3711374 | Nonsyndromic Deafness | 18 | CLINGEN |
ACTG1 | C1858172 | Deafness, Autosomal Dominant 20 | 8 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
ACTG1 | C3281235 | BARAITSER-WINTER SYNDROME 2 | 4 | CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT |
ACTG1 | C0001787 | Osteoporosis, Age-Related | 1 | CTD_human |
ACTG1 | C0005745 | Blepharoptosis | 1 | GENOMICS_ENGLAND |
ACTG1 | C0007097 | Carcinoma | 1 | CTD_human |
ACTG1 | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
ACTG1 | C0009363 | Congenital ocular coloboma (disorder) | 1 | CTD_human |
ACTG1 | C0014544 | Epilepsy | 1 | GENOMICS_ENGLAND |
ACTG1 | C0024433 | Macrostomia | 1 | GENOMICS_ENGLAND |
ACTG1 | C0024667 | Animal Mammary Neoplasms | 1 | CTD_human |
ACTG1 | C0024668 | Mammary Neoplasms, Experimental | 1 | CTD_human |
ACTG1 | C0029456 | Osteoporosis | 1 | CTD_human |
ACTG1 | C0029459 | Osteoporosis, Senile | 1 | CTD_human |
ACTG1 | C0033377 | Ptosis | 1 | GENOMICS_ENGLAND |
ACTG1 | C0205696 | Anaplastic carcinoma | 1 | CTD_human |
ACTG1 | C0205697 | Carcinoma, Spindle-Cell | 1 | CTD_human |
ACTG1 | C0205698 | Undifferentiated carcinoma | 1 | CTD_human |
ACTG1 | C0205699 | Carcinomatosis | 1 | CTD_human |
ACTG1 | C0240583 | Short upturned nose | 1 | GENOMICS_ENGLAND |
ACTG1 | C0265541 | Cranioschisis | 1 | CTD_human |
ACTG1 | C0266551 | Congenital coloboma of iris | 1 | ORPHANET |
ACTG1 | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
ACTG1 | C0497552 | Congenital neurologic anomalies | 1 | CTD_human |
ACTG1 | C0751406 | Post-Traumatic Osteoporosis | 1 | CTD_human |
ACTG1 | C0857379 | Abnormality of the pinna | 1 | GENOMICS_ENGLAND |
ACTG1 | C0948089 | Acute Coronary Syndrome | 1 | CTD_human |
ACTG1 | C1257925 | Mammary Carcinoma, Animal | 1 | CTD_human |
ACTG1 | C1384666 | hearing impairment | 1 | GENOMICS_ENGLAND |
ACTG1 | C1843156 | Progressive sensorineural hearing impairment | 1 | GENOMICS_ENGLAND |
ACTG1 | C1844505 | Pointed chin | 1 | GENOMICS_ENGLAND |
ACTG1 | C1849340 | Long palpebral fissure | 1 | GENOMICS_ENGLAND |
ACTG1 | C1855722 | Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation | 1 | ORPHANET |
ACTG1 | C1865014 | Long philtrum | 1 | GENOMICS_ENGLAND |
ACTG1 | C1865017 | Thin upper lip vermilion | 1 | GENOMICS_ENGLAND |
ACTG1 | C1868571 | Highly arched eyebrow | 1 | GENOMICS_ENGLAND |
ACTG1 | C1970280 | Hearing loss begins with loss of high frequencies | 1 | GENOMICS_ENGLAND |
ACTG1 | C1970281 | Audiogram shows sloping configuration | 1 | GENOMICS_ENGLAND |
ACTG1 | C1970282 | Deafness, profound, by 6th decade | 1 | GENOMICS_ENGLAND |
ACTG1 | C3279369 | Microphthalmia (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C3549665 | Deafness (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C3808883 | Short neck (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4012410 | Enlarged ventricles (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4229649 | Heart defect (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4229650 | Pterygium colli (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4229651 | Hypertelorism/telecanthus | 1 | GENOMICS_ENGLAND |
ACTG1 | C4229652 | Eye coloboma (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4229653 | Trigonocephaly/metopic ridge | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231117 | Pectus (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231118 | Kyphosis/scoliosis (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231120 | Prominent nasal root on profile | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231121 | Large, squared nose tip | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231123 | Retrognathia (in some patients) | 1 | GENOMICS_ENGLAND |
ACTG1 | C4231124 | Prominent/full/wide cheeks | 1 | GENOMICS_ENGLAND |
ACTG1 | C4554007 | Uveoretinal Coloboma | 1 | CTD_human |
ACTG1 | C4708599 | Coloboma of choroid and retina | 1 | ORPHANET |