ENST00000393791.8 ARHGAP9
Information
- Transcript ID
- ENST00000393791.8
- Genome
- hg38
- Position
- chr12:57,472,269-57,479,866
- Strand
- -
- CDS length
- 2,196
- Amino acid length
- 732
- Gene symbol
- ARHGAP9
- Gene type
- protein-coding
- Gene description
- Rho GTPase activating protein 9
- Gene Entrez Gene ID
- 64333
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 |
---|---|---|
18 | 57,472,269 | 57,472,688 |
17 | 57,473,603 | 57,473,708 |
16 | 57,474,042 | 57,474,176 |
15 | 57,474,423 | 57,474,476 |
14 | 57,474,626 | 57,474,703 |
13 | 57,474,875 | 57,474,973 |
12 | 57,475,291 | 57,475,398 |
11 | 57,475,483 | 57,475,615 |
10 | 57,475,833 | 57,475,931 |
9 | 57,476,071 | 57,476,166 |
8 | 57,476,364 | 57,476,454 |
7 | 57,476,590 | 57,476,651 |
6 | 57,476,871 | 57,476,963 |
5 | 57,477,156 | 57,477,269 |
4 | 57,477,459 | 57,477,680 |
3 | 57,478,540 | 57,478,757 |
2 | 57,479,091 | 57,479,424 |
1 | 57,479,730 | 57,479,866 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
18 | CDS | 57,472,517 | 57,472,688 |
17 | CDS | 57,473,603 | 57,473,708 |
16 | CDS | 57,474,042 | 57,474,176 |
15 | CDS | 57,474,423 | 57,474,476 |
14 | CDS | 57,474,626 | 57,474,703 |
13 | CDS | 57,474,875 | 57,474,973 |
12 | CDS | 57,475,291 | 57,475,398 |
11 | CDS | 57,475,483 | 57,475,615 |
10 | CDS | 57,475,833 | 57,475,931 |
9 | CDS | 57,476,071 | 57,476,166 |
8 | CDS | 57,476,364 | 57,476,454 |
7 | CDS | 57,476,590 | 57,476,651 |
6 | CDS | 57,476,871 | 57,476,963 |
5 | CDS | 57,477,156 | 57,477,269 |
4 | CDS | 57,477,459 | 57,477,680 |
3 | CDS | 57,478,540 | 57,478,757 |
2 | CDS | 57,479,091 | 57,479,406 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr12 | 57,866,052 | 57,873,649 | Link |
CDS sequence
ATGCTATCCAGCCGGTGGTGGCCAAGTTCCTGGGGGATCCTAGGGCTGGGCCCCCGAAGCCCTCCTCGGGGATCCCAGCTCTGTGCCCTCTATGCCTTTACTTATACTGGGGCAGATGGCCAGCAGGTGTCTCTGGCTGAAGGGGATAGGTTCCTACTGCTTCGAAAGACCAACTCCGACTGGTGGTTGGCAAGACGCCTAGAAGCTCCCTCCACCTCTCGACCCATCTTCGTCCCAGCAGCCTATATGATAGAGGAATCCATCCCTTCCCAGAGTCCAACTACCGTCATCCCCGGCCAATTGCTCTGGACTCCTGGGCCGAAGTTGTTTCATGGTTCCCTGGAGGAGTTGTCTCAGGCCCTCCCAAGCAGGGCTCAGGCTAGCTCGGAGCAGCCTCCTCCACTTCCCCGCAAAATGTGTAGGAGCGTCAGCACTGACAATCTGAGCCCCAGCCTTCTGAAGCCTTTCCAGGAAGGACCAAGCGGAAGATCCCTCTCCCAGGAAGACTTGCCGTCAGAAGCCAGTGCCAGCACAGCAGGCCCCCAGCCCCTCATGTCAGAGCCCCCTGTGTACTGTAACCTGGTGGACCTTCGCCGCTGTCCTCGGTCCCCACCCCCAGGCCCTGCATGCCCCCTGCTGCAGAGGCTGGATGCCTGGGAGCAGCACCTGGACCCCAACTCTGGACGCTGCTTCTACATAAATTCACTGACTGGCTGCAAGTCCTGGAAGCCCCCGCGCCGCAGTCGCAGCGAGACGAACCCTGGCTCCATGGAGGGGACACAGACCCTGAAGAGGAACAATGATGTCCTGCAACCTCAGGCAAAGGGCTTCAGATCTGACACAGGGACCCCAGAACCGCTTGACCCACAGGGTTCACTCAGCCTCAGCCAACGCACCTCGCAGCTTGACCCTCCAGCCTTGCAGGCCCCTCGACCTCTGCCGCAGCTCCTGGACGACCCCCATGAGGTGGAAAAGTCGGGTCTGCTCAACATGACCAAGATTGCCCAAGGGGGGCGCAAGCTCAGGAAGAACTGGGGCCCGTCTTGGGTGGTGTTAACGGGTAACAGCCTGGTGTTCTACCGAGAGCCACCGCCGACAGCGCCCTCCTCAGGCTGGGGACCAGCGGGTAGCCGGCCCGAAAGTAGCGTGGACCTGCGCGGGGCGGCCCTGGCGCACGGCCGCCACCTGTCCAGCCGCCGCAACGTCCTGCACATCCGCACGATCCCTGGCCACGAGTTCCTGCTGCAGTCGGACCACGAGACAGAGCTGCGAGCCTGGCACCGCGCGCTGCGGACTGTCATCGAGCGGCTGGATCGGGAGAACCCCCTGGAGCTGCGTCTGTCGGGCTCTGGACCCGCGGAGCTGAGCGCCGGGGAGGACGAAGAAGAGGAGTCGGAGCTGGTGTCCAAGCCGCTGCTGCGCCTCAGCAGCCGCCGGAGCTCCATTCGGGGGCCCGAAGGCACCGAGCAGAACCGCGTGCGCAACAAACTAAAGCGGCTCATCGCGAAGAGACCGCCCTTACAAAGCCTGCAGGAGCGGGGTCTGCTCCGAGACCAGGTGTTCGGCTGCCAGTTGGAATCACTCTGCCAGCGGGAAGGAGACACGGTGCCCAGCTTTTTGCGGCTCTGCATTGCTGCTGTGGATAAAAGAGGTCTAGATGTGGATGGCATTTATCGGGTGAGCGGGAACTTGGCAGTGGTCCAGAAGCTTCGCTTTCTGGTGGACAGAGAGCGTGCGGTCACCTCCGATGGGAGGTATGTGTTCCCAGAACAGCCAGGACAAGAAGGTCGGTTAGATTTGGACAGTACTGAGTGGGATGACATTCATGTGGTCACCGGAGCCCTGAAGCTTTTTCTCCGGGAGCTGCCCCAGCCTCTGGTGCCACCACTGCTGCTGCCCCATTTCCGTGCTGCCCTTGCACTCTCCGAATCAGAGCAGTGCCTCTCTCAGATACAAGAATTAATAGGCTCAATGCCAAAGCCCAACCATGACACTCTACGGTACCTCCTGGAGCATTTATGCAGGGTGATAGCACACTCAGATAAGAATCGCATGACACCCCACAACCTGGGAATTGTGTTTGGACCAACCCTGTTTCGGCCAGAGCAGGAGACATCTGACCCAGCAGCCCATGCTCTCTACCCAGGGCAGCTGGTCCAGCTGATGCTCACCAACTTCACCAGCCTCTTCCCCTGA
Amino sequence
MLSSRWWPSSWGILGLGPRSPPRGSQLCALYAFTYTGADGQQVSLAEGDRFLLLRKTNSDWWLARRLEAPSTSRPIFVPAAYMIEESIPSQSPTTVIPGQLLWTPGPKLFHGSLEELSQALPSRAQASSEQPPPLPRKMCRSVSTDNLSPSLLKPFQEGPSGRSLSQEDLPSEASASTAGPQPLMSEPPVYCNLVDLRRCPRSPPPGPACPLLQRLDAWEQHLDPNSGRCFYINSLTGCKSWKPPRRSRSETNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQAPRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSRRNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLDRENPLELRLSGSGPAELSAGEDEEEESELVSKPLLRLSSRRSSIRGPEGTEQNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRVSGNLAVVQKLRFLVDRERAVTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQIQELIGSMPKPNHDTLRYLLEHLCRVIAHSDKNRMTPHNLGIVFGPTLFRPEQETSDPAAHALYPGQLVQLMLTNFTSLFP*