ENST00000686984.1 VSIG10L2
Information
- Transcript ID
- ENST00000686984.1
- Genome
- hg38
- Position
- chr11:125,946,044-125,956,319
- 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 | 125,946,044 | 125,946,137 |
| 2 | 125,947,686 | 125,948,036 |
| 3 | 125,948,305 | 125,948,580 |
| 4 | 125,950,014 | 125,950,289 |
| 5 | 125,950,910 | 125,951,158 |
| 6 | 125,951,813 | 125,952,073 |
| 7 | 125,953,400 | 125,953,690 |
| 8 | 125,954,087 | 125,954,383 |
| 9 | 125,955,057 | 125,955,179 |
| 10 | 125,955,482 | 125,955,506 |
| 11 | 125,955,615 | 125,955,667 |
| 12 | 125,955,817 | 125,956,319 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 125,946,056 | 125,946,137 |
| 2 | CDS | 125,947,686 | 125,948,036 |
| 3 | CDS | 125,948,305 | 125,948,580 |
| 4 | CDS | 125,950,014 | 125,950,289 |
| 5 | CDS | 125,950,910 | 125,951,158 |
| 6 | CDS | 125,951,813 | 125,952,073 |
| 7 | CDS | 125,953,400 | 125,953,690 |
| 8 | CDS | 125,954,087 | 125,954,383 |
| 9 | CDS | 125,955,057 | 125,955,179 |
| 10 | CDS | 125,955,482 | 125,955,506 |
| 11 | CDS | 125,955,615 | 125,955,667 |
| 12 | CDS | 125,955,817 | 125,955,914 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr11 | 125,815,939 | 125,826,214 | Link |
CDS sequence
ATGGTGGGTCAGAGGGCCCAGCACAGCCCAGTCAGCCTCCTGCTGCTGATACACCTCTGCCTTCTGCACCTGAGGGCCTCAGGCCAGCCCCACCCGACCCCCGAGGCCCCTGTAGAGGAGGTGGTGTCTGTCCAGGGAGTGCGAGGTGGCTCCGTGGAGCTGGCCTGTGGCTCAGGGCCTGCCCCGCTGCTGGTCCTCTGGAGCTTCACCCCCCTGGGCTCCCTGGTTCCCCGGCCTGTGGCCGTCACCGATGGAGCCATGTCCAAGGTGGAGGCCATCGCCTCGGCTCTGGGAGTCGTGAGTCTGAGGAACAGCAGCCTGGTGCTGGGGGAGCTTCACGAGGGTGCCCGTGGCCACTTCCTATGCCAGGTTCTGCACGTGGCTGGCGGCCAGCTCCACGCTGCCTACTCCCACCTCACGCTGGCTGTGCTGGTGCCGGTGTCCAAGCCTCAAGTGCGACTGAGTAACCCGTCCCCTGTGGAGGGAGCCTCCGTGGTGGCCACGTGTGCAGTGCGGGAGGGCACAGAGCCCGTGACCTTTGCCTGGCAGCATCGGGCACCCCGAGGCCTTGGAGAGGCCCTGGTGGGGGTCACTGAGCCACTATTCCAGCTGGACCCTGTCAACCGGACACACCTAGGGTGGTACATGTGCAGCGCCAGCAACTCCGTGAACAGGCTGAGCAGTGACGGGGCCTTCCTGGACGTCATTTATGGTCCTGACAAGCCTGTGATCACCATGGAGCCGCTGGGACTCACTGAGGAGGGCTTCTGGGCCAGTGAGAGGGAAGAGGTGACCCTGAGCTGTCTGGCTGCCTCCAACCCACCTAGTCACTATGTGTGGCTCCGTGACCACACGCAAGTCCACACGGGGCCTACCTATGTCATCGCCAGAGCTGGCCGTGTCCACACAGGCCTGTACACCTGCCTGGCCCGCAACAGCTACCTGGACACCCGCACCCAGACTACTGTCCAGCTCACCATCTACTATCCCCCTGAGGGACAGCCCTCCTGTGCAGTGCATCCCAGCCCTGAGGCTGTGACCCTGCTCTGTGCCTGGCCTGGGGGGCTTCCGCCTGCCCAACTGCAGTGGGAAGGGCCTCAGGGACCTGGCCCTACTGCCCCCAGCAACGTCACCTGGAGTCACGCAGCCGCCCAGCTCCCCAGTGGCAGCGTCTTCACCTGCACTGGCCAGCACCCAGCCCTGGCACCGCCTGCCCTCTGCACAGTCATGCTCTGGGAGCCTCTCGGGAGGCCTACCTGCTGGAGCACAGCCACAATGGGGGACCAGTTCATCATGCTGAGCTGCGAGTGGCCTGGCGGCGAGCCCCCTGCCACGCTGGGCTGGCTTGACGAACAGCAGCAGCCCCTGGGCGGCAGCAGCTCCTCGATGGCCGTTCACCTCCTGCAGGCCCAAGAAGATCTGGCTGGCAGAGAGTTCACCTGCCGGGGCACTCACCTGCTCAGGACCCCTGACCCCCACTGCCACCTCCAGCTGGAAGCCCCACAGCTGGACGTGGCTGAGCCCCGCGTGTCAGTGTTGGAGGGGGGAGAGGCCTGGCTGGAGTGCTCTCTCCGCGGGGGCACACCACCTGCCCAGCTCCTCTGGCTGGGGCCTCAACAACAAAAAGTGGACCCCGGCACTTCAGGATTCATGCTGCACCCTGAGGGTGCCCAGCTGCGCCTGGGCATCTACGATGCTGACCCGGCACACCACAGGGGCACCTACCAATGCGTGGCCCGCAACGCCGTGGGCAATAGCAGTCAGAGTGTGCTGCTGGAGGTCCTGAGATATCCAGCTCCTCCCAATGTCACCATCAGCCGCCTGACCTACGGGAGGCACCGGAGAGAGGTGCAGCTTCAATGGGCCATCTTAGGACCCGGGAACCTGACGGGCTTCCTGGTGCAGCGGAAGGCCAGTGCCCTGGGCCCAGGAGCTGGGGCGTGGGAGACAGCAGCTAGTGACATCGAGCCAGAGAGCCGAGGACGGCGGCTGGGGGGCTTGGACCCCGGGGTCCTTTATGCCTTCCGCATCCTGGCTCTGAATCACCACACTGCAGGACATCCCTCTGAGGTGAAGATACCAGCGGACCCCCCCTTCAGCGCCTACCCAGCGGTGTTGGGTGCAGCAGGCACGGGAATGGTGGTAGCAACGGTGGCCTCTCTACTGGTGTTCCAGTATGCTGCCCGGCACCCAGAGACTTTCCCCCGCCTTGGTCAATTGCTTGTTCCCACGGAGCAAAGGCACCAACAGAGGGGTTCCAGAGAAGATGCTGAGGCACCGGCAGGCCTTGAAACACCAACCACCACCCCAGGTTTGGATCCTGCACAAGAAACCACGGATTCTCCAGTGAATGTCACCATCACAGTGACTGCAACACCATAA
Amino sequence
MVGQRAQHSPVSLLLLIHLCLLHLRASGQPHPTPEAPVEEVVSVQGVRGGSVELACGSGPAPLLVLWSFTPLGSLVPRPVAVTDGAMSKVEAIASALGVVSLRNSSLVLGELHEGARGHFLCQVLHVAGGQLHAAYSHLTLAVLVPVSKPQVRLSNPSPVEGASVVATCAVREGTEPVTFAWQHRAPRGLGEALVGVTEPLFQLDPVNRTHLGWYMCSASNSVNRLSSDGAFLDVIYGPDKPVITMEPLGLTEEGFWASEREEVTLSCLAASNPPSHYVWLRDHTQVHTGPTYVIARAGRVHTGLYTCLARNSYLDTRTQTTVQLTIYYPPEGQPSCAVHPSPEAVTLLCAWPGGLPPAQLQWEGPQGPGPTAPSNVTWSHAAAQLPSGSVFTCTGQHPALAPPALCTVMLWEPLGRPTCWSTATMGDQFIMLSCEWPGGEPPATLGWLDEQQQPLGGSSSSMAVHLLQAQEDLAGREFTCRGTHLLRTPDPHCHLQLEAPQLDVAEPRVSVLEGGEAWLECSLRGGTPPAQLLWLGPQQQKVDPGTSGFMLHPEGAQLRLGIYDADPAHHRGTYQCVARNAVGNSSQSVLLEVLRYPAPPNVTISRLTYGRHRREVQLQWAILGPGNLTGFLVQRKASALGPGAGAWETAASDIEPESRGRRLGGLDPGVLYAFRILALNHHTAGHPSEVKIPADPPFSAYPAVLGAAGTGMVVATVASLLVFQYAARHPETFPRLGQLLVPTEQRHQQRGSREDAEAPAGLETPTTTPGLDPAQETTDSPVNVTITVTATP*