ENST00000686984.1 VSIG10L2
Information
- Transcript ID
- ENST00000686984.1
- Genome
- hg19
- Position
- chr11:125,815,939-125,826,214
- Strand
- +
- CDS length
- 2,382
- Amino acid length
- 794
- Gene symbol
- VSIG10L2
- Gene type
- protein-coding
- Gene description
- V-set and immunoglobulin domain containing 10 like 2
- Gene Entrez Gene ID
- 338667
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 | 125,815,939 | 125,816,032 |
| 2 | 125,817,581 | 125,817,931 |
| 3 | 125,818,200 | 125,818,475 |
| 4 | 125,819,909 | 125,820,184 |
| 5 | 125,820,805 | 125,821,053 |
| 6 | 125,821,708 | 125,821,968 |
| 7 | 125,823,295 | 125,823,585 |
| 8 | 125,823,982 | 125,824,278 |
| 9 | 125,824,952 | 125,825,074 |
| 10 | 125,825,377 | 125,825,401 |
| 11 | 125,825,510 | 125,825,562 |
| 12 | 125,825,712 | 125,826,214 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 125,815,951 | 125,816,032 |
| 2 | CDS | 125,817,581 | 125,817,931 |
| 3 | CDS | 125,818,200 | 125,818,475 |
| 4 | CDS | 125,819,909 | 125,820,184 |
| 5 | CDS | 125,820,805 | 125,821,053 |
| 6 | CDS | 125,821,708 | 125,821,968 |
| 7 | CDS | 125,823,295 | 125,823,585 |
| 8 | CDS | 125,823,982 | 125,824,278 |
| 9 | CDS | 125,824,952 | 125,825,074 |
| 10 | CDS | 125,825,377 | 125,825,401 |
| 11 | CDS | 125,825,510 | 125,825,562 |
| 12 | CDS | 125,825,712 | 125,825,809 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr11 | 125,946,044 | 125,956,319 | Link |
CDS sequence
ATGGTGGGTCAGAGGGCCCAGCACAGCCCAGTCAGCCTCCTGCTGCTGATACACCTCTGCCTTCTGCACCTGAGGGCCTCAGGCCAGCCCCACCCGACCCCCGAGGCCCCTGTAGAGGAGGTGGTGTCTGTCCAGGGAGTGCGAGGTGGCTCCGTGGAGCTGGCCTGTGGCTCAGGGCCTGCCCCGCTGCTGGTCCTCTGGAGCTTCACCCCCCTGGGCTCCCTGGTTCCCCGGCCTGTGGCCGTCACCGATGGAGCCATGTCCAAGGTGGAGGCCATCGCCTCGGCTCTGGGAGTCGTGAGTCTGAGGAACAGCAGCCTGGTGCTGGGGGAGCTTCACGAGGGTGCCCGTGGCCACTTCCTATGCCAGGTTCTGCACGTGGCTGGCGGCCAGCTCCACGCTGCCTACTCCCACCTCACGCTGGCTGTGCTGGTGCCGGTGTCCAAGCCTCAAGTGCGACTGAGTAACCCGTCCCCTGTGGAGGGAGCCTCCGTGGTGGCCACGTGTGCAGTGCGGGAGGGCACAGAGCCCGTGACCTTTGCCTGGCAGCATCGGGCACCCCGAGGCCTTGGAGAGGCCCTGGTGGGGGTCACTGAGCCACTATTCCAGCTGGACCCTGTCAACCGGACACACCTAGGGTGGTACATGTGCAGCGCCAGCAACTCCGTGAACAGGCTGAGCAGTGACGGGGCCTTCCTGGACGTCATTTATGGTCCTGACAAGCCTGTGATCACCATGGAGCCGCTGGGACTCACTGAGGAGGGCTTCTGGGCCAGTGAGAGGGAAGAGGTGACCCTGAGCTGTCTGGCTGCCTCCAACCCACCTAGTCACTATGTGTGGCTCCGTGACCACACGCAAGTCCACACGGGGCCTACCTATGTCATCGCCAGAGCTGGCCGTGTCCACACAGGCCTGTACACCTGCCTGGCCCGCAACAGCTACCTGGACACCCGCACCCAGACTACTGTCCAGCTCACCATCTACTATCCCCCTGAGGGACAGCCCTCCTGTGCAGTGCATCCCAGCCCTGAGGCTGTGACCCTGCTCTGTGCCTGGCCTGGGGGGCTTCCGCCTGCCCAACTGCAGTGGGAAGGGCCTCAGGGACCTGGCCCTACTGCCCCCAGCAACGTCACCTGGAGTCACGCAGCCGCCCAGCTCCCCAGTGGCAGCGTCTTCACCTGCACTGGCCAGCACCCAGCCCTGGCACCGCCTGCCCTCTGCACAGTCATGCTCTGGGAGCCTCTCGGGAGGCCTACCTGCTGGAGCACAGCCACAATGGGGGACCAGTTCATCATGCTGAGCTGCGAGTGGCCTGGCGGCGAGCCCCCTGCCACGCTGGGCTGGCTTGACGAACAGCAGCAGCCCCTGGGCGGCAGCAGCTCCTCGATGGCCGTTCACCTCCTGCAGGCCCAAGAAGATCTGGCTGGCAGAGAGTTCACCTGCCGGGGCACTCACCTGCTCAGGACCCCTGACCCCCACTGCCACCTCCAGCTGGAAGCCCCACAGCTGGACGTGGCTGAGCCCCGCGTGTCAGTGTTGGAGGGGGGAGAGGCCTGGCTGGAGTGCTCTCTCCGCGGGGGCACACCACCTGCCCAGCTCCTCTGGCTGGGGCCTCAACAACAAAAAGTGGACCCCGGCACTTCAGGATTCATGCTGCACCCTGAGGGTGCCCAGCTGCGCCTGGGCATCTACGATGCTGACCCGGCACACCACAGGGGCACCTACCAATGCGTGGCCCGCAACGCCGTGGGCAATAGCAGTCAGAGTGTGCTGCTGGAGGTCCTGAGATATCCAGCTCCTCCCAATGTCACCATCAGCCGCCTGACCTACGGGAGGCACCGGAGAGAGGTGCAGCTTCAATGGGCCATCTTAGGACCCGGGAACCTGACGGGCTTCCTGGTGCAGCGGAAGGCCAGTGCCCTGGGCCCAGGAGCTGGGGCGTGGGAGACAGCAGCTAGTGACATCGAGCCAGAGAGCCGAGGACGGCGGCTGGGGGGCTTGGACCCCGGGGTCCTTTATGCCTTCCGCATCCTGGCTCTGAATCACCACACTGCAGGACATCCCTCTGAGGTGAAGATACCAGCGGACCCCCCCTTCAGCGCCTACCCAGCGGTGTTGGGTGCAGCAGGCACGGGAATGGTGGTAGCAACGGTGGCCTCTCTACTGGTGTTCCAGTATGCTGCCCGGCACCCAGAGACTTTCCCCCGCCTTGGTCAATTGCTTGTTCCCACGGAGCAAAGGCACCAACAGAGGGGTTCCAGAGAAGATGCTGAGGCACCGGCAGGCCTTGAAACACCAACCACCACCCCAGGTTTGGATCCTGCACAAGAAACCACGGATTCTCCAGTGAATGTCACCATCACAGTGACTGCAACACCATAA
Amino sequence
MVGQRAQHSPVSLLLLIHLCLLHLRASGQPHPTPEAPVEEVVSVQGVRGGSVELACGSGPAPLLVLWSFTPLGSLVPRPVAVTDGAMSKVEAIASALGVVSLRNSSLVLGELHEGARGHFLCQVLHVAGGQLHAAYSHLTLAVLVPVSKPQVRLSNPSPVEGASVVATCAVREGTEPVTFAWQHRAPRGLGEALVGVTEPLFQLDPVNRTHLGWYMCSASNSVNRLSSDGAFLDVIYGPDKPVITMEPLGLTEEGFWASEREEVTLSCLAASNPPSHYVWLRDHTQVHTGPTYVIARAGRVHTGLYTCLARNSYLDTRTQTTVQLTIYYPPEGQPSCAVHPSPEAVTLLCAWPGGLPPAQLQWEGPQGPGPTAPSNVTWSHAAAQLPSGSVFTCTGQHPALAPPALCTVMLWEPLGRPTCWSTATMGDQFIMLSCEWPGGEPPATLGWLDEQQQPLGGSSSSMAVHLLQAQEDLAGREFTCRGTHLLRTPDPHCHLQLEAPQLDVAEPRVSVLEGGEAWLECSLRGGTPPAQLLWLGPQQQKVDPGTSGFMLHPEGAQLRLGIYDADPAHHRGTYQCVARNAVGNSSQSVLLEVLRYPAPPNVTISRLTYGRHRREVQLQWAILGPGNLTGFLVQRKASALGPGAGAWETAASDIEPESRGRRLGGLDPGVLYAFRILALNHHTAGHPSEVKIPADPPFSAYPAVLGAAGTGMVVATVASLLVFQYAARHPETFPRLGQLLVPTEQRHQQRGSREDAEAPAGLETPTTTPGLDPAQETTDSPVNVTITVTATP*