ENST00000379663.7 EXOSC9
Information
- Transcript ID
- ENST00000379663.7
- Genome
- hg19
- Position
- chr4:122,722,475-122,738,064
- Strand
- +
- CDS length
- 1,371
- Amino acid length
- 457
- Gene symbol
- EXOSC9
- Gene type
- protein-coding
- Gene description
- exosome component 9
- Gene Entrez Gene ID
- 5393
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Exon
Exon number | Start | Stop |
---|---|---|
1 | 122,722,475 | 122,722,645 |
2 | 122,722,982 | 122,723,076 |
3 | 122,723,829 | 122,723,948 |
4 | 122,724,070 | 122,724,172 |
5 | 122,725,777 | 122,725,914 |
6 | 122,728,695 | 122,728,777 |
7 | 122,731,122 | 122,731,254 |
8 | 122,732,738 | 122,732,826 |
9 | 122,734,389 | 122,734,535 |
10 | 122,735,021 | 122,735,202 |
11 | 122,737,299 | 122,737,349 |
12 | 122,737,524 | 122,737,602 |
13 | 122,737,927 | 122,738,064 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 122,722,580 | 122,722,645 |
2 | CDS | 122,722,982 | 122,723,076 |
3 | CDS | 122,723,829 | 122,723,948 |
4 | CDS | 122,724,070 | 122,724,172 |
5 | CDS | 122,725,777 | 122,725,914 |
6 | CDS | 122,728,695 | 122,728,777 |
7 | CDS | 122,731,122 | 122,731,254 |
8 | CDS | 122,732,738 | 122,732,826 |
9 | CDS | 122,734,389 | 122,734,535 |
10 | CDS | 122,735,021 | 122,735,202 |
11 | CDS | 122,737,299 | 122,737,349 |
12 | CDS | 122,737,524 | 122,737,602 |
13 | CDS | 122,737,927 | 122,738,011 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr4 | 121,801,320 | 121,816,909 | Link |
CDS sequence
ATGAAGGAAACGCCACTCTCAAACTGCGAACGCCGCTTCCTACTCCGTGCCATCGAAGAGAAGAAGCGGCTGGATGGCAGACAAACCTATGATTATAGGAACATCAGGATCTCATTTGGAACAGATTACGGATGCTGCATTGTGGAACTTGGAAAAACAAGAGTTCTTGGACAGGTTTCCTGTGAACTTGTGTCTCCAAAACTCAATCGGGCAACAGAAGGTATTCTTTTTTTTAACCTTGAACTCTCTCAGATGGCCGCTCCAGCTTTCGAACCTGGCAGGCAGTCAGATCTCTTGGTGAAGTTGAATCGACTCATGGAAAGATGTCTAAGAAATTCGAAGTGTATAGACACTGAGTCTCTCTGTGTTGTTGCTGGTGAAAAGGTTTGGCAAATACGTGTAGACCTACATTTATTAAATCATGATGGAAATATTATTGATGCTGCCAGCATTGCTGCAATCGTGGCCTTATGTCATTTCCGAAGACCTGATGTCTCTGTCCAAGGAGATGAAGTAACACTGTATACACCTGAAGAGCGTGATCCTGTACCATTAAGTATCCACCACATGCCCATTTGTGTCAGTTTTGCCTTTTTCCAGCAAGGAACATATTTATTGGTGGATCCCAATGAACGAGAAGAACGTGTGATGGATGGCTTGCTGGTGATTGCCATGAACAAACATCGAGAGATTTGTACTATCCAGTCCAGTGGTGGGATAATGCTACTAAAAGATCAAGTTCTGAGATGCAGTAAAATCGCTGGTGTGAAAGTAGCAGAAATTACAGAGCTAATATTGAAAGCTTTGGAGAATGACCAAAAAGTAAGGAAAGAAGGTGGAAAGTTTGGTTTTGCAGAGTCTATAGCAAATCAAAGGATCACAGCATTTAAAATGGAAAAGGCCCCTATTGATACCTCGGATGTAGAAGAAAAAGCAGAAGAAATCATTGCTGAAGCAGAACCTCCTTCAGAAGTTGTTTCTACACCTGTGCTATGGACTCCTGGAACTGCCCAAATTGGAGAGGGAGTAGAAAACTCCTGGGGTGATCTTGAAGACTCTGAGAAGGAAGATGATGAAGGCGGTGGTGATCAAGCTATCATTCTTGATGGTATAAAAATGGACACTGGAGTAGAAGTCTCTGATATTGGAAGCCAAGAGCTGGGGTTTCACCATGTTGGCCAGACTGGACTCGAGTTCCTGACCTCAGATGCTCCCATAATACTCTCAGATAGTGAAGAAGAAGAAATGATCATTTTGGAACCAGACAAGAATCCAAAGAAAATAAGAACACAGACCACCAGTGCAAAACAAGAAAAAGCACCAAGTAAAAAGCCAGTGAAAAGAAGAAAAAAGAAGAGAGCTGCCAATTAA
Amino sequence
MKETPLSNCERRFLLRAIEEKKRLDGRQTYDYRNIRISFGTDYGCCIVELGKTRVLGQVSCELVSPKLNRATEGILFFNLELSQMAAPAFEPGRQSDLLVKLNRLMERCLRNSKCIDTESLCVVAGEKVWQIRVDLHLLNHDGNIIDAASIAAIVALCHFRRPDVSVQGDEVTLYTPEERDPVPLSIHHMPICVSFAFFQQGTYLLVDPNEREERVMDGLLVIAMNKHREICTIQSSGGIMLLKDQVLRCSKIAGVKVAEITELILKALENDQKVRKEGGKFGFAESIANQRITAFKMEKAPIDTSDVEEKAEEIIAEAEPPSEVVSTPVLWTPGTAQIGEGVENSWGDLEDSEKEDDEGGGDQAIILDGIKMDTGVEVSDIGSQELGFHHVGQTGLEFLTSDAPIILSDSEEEEMIILEPDKNPKKIRTQTTSAKQEKAPSKKPVKRRKKKRAAN*