ENST00000642475.1 TM9SF2
Information
- Transcript ID
- ENST00000642475.1
- Genome
- hg38
- Position
- chr13:99,498,956-99,563,334
- Strand
- +
- CDS length
- 1,992
- Amino acid length
- 664
- Gene symbol
- TM9SF2
- Gene type
- protein-coding
- Gene description
- transmembrane 9 superfamily member 2
- Gene Entrez Gene ID
- 9375
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
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 | 99,498,956 | 99,499,469 |
2 | 99,500,597 | 99,500,784 |
3 | 99,501,019 | 99,501,777 |
4 | 99,517,614 | 99,517,681 |
5 | 99,520,036 | 99,520,129 |
6 | 99,529,467 | 99,529,594 |
7 | 99,536,608 | 99,536,737 |
8 | 99,537,739 | 99,537,863 |
9 | 99,539,446 | 99,539,557 |
10 | 99,540,714 | 99,540,793 |
11 | 99,541,559 | 99,541,667 |
12 | 99,543,863 | 99,543,995 |
13 | 99,546,985 | 99,547,104 |
14 | 99,549,165 | 99,549,222 |
15 | 99,552,167 | 99,552,326 |
16 | 99,554,304 | 99,554,455 |
17 | 99,555,536 | 99,555,647 |
18 | 99,559,363 | 99,559,534 |
19 | 99,562,691 | 99,563,334 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
3 | CDS | 99,501,607 | 99,501,777 |
4 | CDS | 99,517,614 | 99,517,681 |
5 | CDS | 99,520,036 | 99,520,129 |
6 | CDS | 99,529,467 | 99,529,594 |
7 | CDS | 99,536,608 | 99,536,737 |
8 | CDS | 99,537,739 | 99,537,863 |
9 | CDS | 99,539,446 | 99,539,557 |
10 | CDS | 99,540,714 | 99,540,793 |
11 | CDS | 99,541,559 | 99,541,667 |
12 | CDS | 99,543,863 | 99,543,995 |
13 | CDS | 99,546,985 | 99,547,104 |
14 | CDS | 99,549,165 | 99,549,222 |
15 | CDS | 99,552,167 | 99,552,326 |
16 | CDS | 99,554,304 | 99,554,455 |
17 | CDS | 99,555,536 | 99,555,647 |
18 | CDS | 99,559,363 | 99,559,534 |
19 | CDS | 99,562,691 | 99,562,758 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr13 | 100,151,210 | 100,215,588 | Link |
CDS sequence
ATGAGCGCGAGGCTGCCGGTGTTGTCTCCACCTCGGTGGCCGCGGCTGTTGCTGCTGTCGCTGCTCCTGCTGGGGGCGGTTCCTGGCCCGCGCCGGAGCGGCGCTTTCTACCTGCCCGGCCTGGCGCCCGTCAACTTCTGCGACGAAGAAAAAAAGAGCGACGAGTGCAAGGCCGAAATAGAACTATTTGTGAACAGACTTGATTCAGTGGAATCAGTTCTTCCTTATGAATACACAGCGTTTGATTTTTGCCAAGCATCAGAAGGAAAGCGCCCATCTGAAAATCTTGGTCAGGTACTATTCGGGGAAAGAATTGAACCTTCACCATATAAGTTTACGTTTAATAAGAAGGAGACCTGTAAGCTTGTTTGTACAAAAACATACCATACAGAGAAAGCTGAAGACAAACAAAAGTTAGAATTCTTGAAAAAAAGCATGTTATTGAATTATCAACATCACTGGATTGTGGATAATATGCCTGTAACGTGGTGTTACGATGTTGAAGATGGTCAGAGGTTCTGTAATCCTGGATTTCCTATTGGCTGTTACATTACAGATAAAGGCCATGCAAAAGATGCCTGTGTTATTAGTTCAGATTTCCATGAAAGAGATACATTTTACATCTTCAACCATGTTGACATCAAAATATACTATCATGTTGTTGAAACTGGGTCCATGGGAGCAAGATTAGTGGCTGCTAAACTTGAACCGAAAAGCTTCAAACATACCCATATAGATAAACCAGACTGCTCAGGGCCCCCCATGGACATAAGTAACAAGGCTTCTGGGGAGATAAAAATTGCCTATACTTACTCTGTTAGCTTCGAGGAAGATGATAAGATCAGATGGGCGTCTAGATGGGACTATATTCTGGAGTCTATGCCTCATACCCACATTCAGTGGTTTAGCATTATGAATTCCCTGGTCATTGTTCTCTTCTTATCTGGAATGGTAGCTATGATTATGTTACGGACACTGCACAAAGATATTGCTAGATATAATCAGATGGACTCTACGGAAGATGCCCAGGAAGAATTTGGCTGGAAACTTGTTCATGGTGATATATTCCGTCCTCCAAGAAAAGGGATGCTGCTATCAGTCTTTCTAGGATCCGGGACACAGATTTTAATTATGACCTTTGTGACTCTATTTTTCGCTTGCCTGGGATTTTTGTCACCTGCCAACCGAGGAGCGCTGATGACGTGTGCTGTGGTCCTGTGGGTGCTGCTGGGCACCCCTGCAGGCTATGTTGCTGCCAGATTCTATAAGTCCTTTGGAGGTGAGAAGTGGAAAACAAATGTTTTATTAACATCATTTCTTTGTCCTGGGATTGTATTTGCTGACTTCTTTATAATGAATCTGATCCTCTGGGGAGAAGGATCTTCAGCAGCTATTCCTTTTGGGACACTGGTTGCCATATTGGCCCTTTGGTTCTGCATATCTGTGCCTCTGACGTTTATTGGTGCATACTTTGGTTTTAAGAAGAATGCCATTGAACACCCAGTTCGAACCAATCAGATTCCACGTCAGATTCCTGAACAGTCGTTCTACACGAAGCCCTTGCCTGGTATTATCATGGGAGGGATTTTGCCCTTTGGCTGCATCTTTATACAACTTTTCTTCATTCTGAATAGTATTTGGTCACACCAGATGTATTACATGTTTGGCTTCCTATTTCTGGTGTTTATCATTTTGGTTATTACCTGTTCTGAAGCAACTATACTTCTTTGCTATTTCCACCTATGTGCAGAGGATTATCATTGGCAATGGCGTTCATTCCTTACGAGTGGCTTTACTGCAGTTTATTTCTTAATCTATGCAGTACACTACTTCTTTTCAAAACTGCAGATCACGGGAACAGCAAGCACAATTCTGTACTTTGGTTATACCATGATAATGGTTTTGATCTTCTTTCTTTTTACAGGAACAATTGGCTTCTTTGCATGCTTTTGGTTTGTTACCAAAATATACAGTGTGGTGAAGGTTGACTGA
Amino sequence
MSARLPVLSPPRWPRLLLLSLLLLGAVPGPRRSGAFYLPGLAPVNFCDEEKKSDECKAEIELFVNRLDSVESVLPYEYTAFDFCQASEGKRPSENLGQVLFGERIEPSPYKFTFNKKETCKLVCTKTYHTEKAEDKQKLEFLKKSMLLNYQHHWIVDNMPVTWCYDVEDGQRFCNPGFPIGCYITDKGHAKDACVISSDFHERDTFYIFNHVDIKIYYHVVETGSMGARLVAAKLEPKSFKHTHIDKPDCSGPPMDISNKASGEIKIAYTYSVSFEEDDKIRWASRWDYILESMPHTHIQWFSIMNSLVIVLFLSGMVAMIMLRTLHKDIARYNQMDSTEDAQEEFGWKLVHGDIFRPPRKGMLLSVFLGSGTQILIMTFVTLFFACLGFLSPANRGALMTCAVVLWVLLGTPAGYVAARFYKSFGGEKWKTNVLLTSFLCPGIVFADFFIMNLILWGEGSSAAIPFGTLVAILALWFCISVPLTFIGAYFGFKKNAIEHPVRTNQIPRQIPEQSFYTKPLPGIIMGGILPFGCIFIQLFFILNSIWSHQMYYMFGFLFLVFIILVITCSEATILLCYFHLCAEDYHWQWRSFLTSGFTAVYFLIYAVHYFFSKLQITGTASTILYFGYTMIMVLIFFLFTGTIGFFACFWFVTKIYSVVKVD*