ENST00000261191.12 INTS13
Information
- Transcript ID
- ENST00000261191.12
- Genome
- hg38
- Position
- chr12:26,905,181-26,937,981
- Strand
- -
- CDS length
- 2,121
- Amino acid length
- 707
- Gene symbol
- INTS13
- Gene type
- protein-coding
- Gene description
- integrator complex subunit 13
- Gene Entrez Gene ID
- 55726
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 |
|---|---|---|
| 17 | 26,905,181 | 26,905,536 |
| 16 | 26,906,302 | 26,906,437 |
| 15 | 26,911,178 | 26,911,317 |
| 14 | 26,913,457 | 26,913,687 |
| 13 | 26,913,974 | 26,914,128 |
| 12 | 26,914,408 | 26,914,578 |
| 11 | 26,916,002 | 26,916,180 |
| 10 | 26,917,352 | 26,917,441 |
| 9 | 26,917,644 | 26,917,733 |
| 8 | 26,922,616 | 26,922,700 |
| 7 | 26,924,355 | 26,924,483 |
| 6 | 26,925,761 | 26,925,851 |
| 5 | 26,928,205 | 26,928,285 |
| 4 | 26,928,703 | 26,928,905 |
| 3 | 26,934,556 | 26,934,630 |
| 2 | 26,936,579 | 26,936,814 |
| 1 | 26,937,796 | 26,937,981 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 17 | CDS | 26,905,497 | 26,905,536 |
| 16 | CDS | 26,906,302 | 26,906,437 |
| 15 | CDS | 26,911,178 | 26,911,317 |
| 14 | CDS | 26,913,457 | 26,913,687 |
| 13 | CDS | 26,913,974 | 26,914,128 |
| 12 | CDS | 26,914,408 | 26,914,578 |
| 11 | CDS | 26,916,002 | 26,916,180 |
| 10 | CDS | 26,917,352 | 26,917,441 |
| 9 | CDS | 26,917,644 | 26,917,733 |
| 8 | CDS | 26,922,616 | 26,922,700 |
| 7 | CDS | 26,924,355 | 26,924,483 |
| 6 | CDS | 26,925,761 | 26,925,851 |
| 5 | CDS | 26,928,205 | 26,928,285 |
| 4 | CDS | 26,928,703 | 26,928,905 |
| 3 | CDS | 26,934,556 | 26,934,630 |
| 2 | CDS | 26,936,579 | 26,936,803 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr12 | 27,058,114 | 27,090,914 | Link |
CDS sequence
ATGAAGATTTTTTCTGAATCTCATAAAACAGTGTTTGTTGTGGATCACTGCCCTTATATGGCAGAATCTTGCAGGCAGCATGTCGAGTTTGATATGCTGGTGAAGAATAGAACCCAAGGAATCATTCCTTTGGCCCCCATATCTAAATCATTGTGGACTTGCTCAGTAGAATCTTCCATGGAATATTGTAGAATAATGTATGATATATTTCCTTTCAAAAAGCTGGTGAATTTTATTGTGAGTGACTCTGGAGCACATGTTTTAAATTCTTGGACTCAAGAAGACCAAAATTTACAGGAGCTAATGGCAGCATTAGCCGCTGTTGGGCCTCCTAATCCTCGGGCAGATCCAGAGTGCTGCAGTATTCTGCATGGCCTTGTTGCAGCAGTGGAAACTCTCTGCAAAATTACTGAATACCAACATGAGGCTCGTACTCTACTCATGGAGAATGCAGAACGTGTTGGAAATAGAGGACGAATAATCTGTATTACTAATGCAAAAAGTGATAGTCATGTGCGAATGCTTGAAGACTGTGTCCAGGAAACGATTCATGAACATAACAAGCTTGCTGCAAATTCAGATCATCTCATGCAGATTCAAAAATGTGAGTTGGTCTTGATCCACACCTACCCAGTTGGTGAAGACAGCCTTGTATCTGATCGTTCTAAAAAAGAGTTGTCCCCGGTTTTAACCAGTGAAGTTCATAGTGTTCGTGCAGGACGGCATCTTGCTACCAAATTGAATATTTTAGTACAGCAACATTTTGACTTGGCTTCAACTACTATTACAAATATTCCAATGAAGGAAGAACAGCATGCTAACACATCTGCCAATTATGATGTGGAGCTACTTCATCACAAAGATGCACATGTAGATTTCCTGAAAAGTGGTGATTCGCATCTAGGTGGCGGCAGTCGAGAAGGCTCGTTTAAAGAAACAATAACATTAAAGTGGTGTACACCAAGGACAAATAACATTGAATTACACTATTGTACTGGAGCTTATCGGATTTCACCTGTAGATGTAAATAGTAGACCTTCCTCCTGCCTTACTAATTTTCTTCTAAATGGTCGTTCTGTTTTATTGGAACAACCACGAAAGTCAGGTTCTAAAGTCATTAGTCATATGCTTAGTAGCCATGGAGGAGAGATTTTTTTGCACGTCCTTAGCAGTTCTCGATCCATTCTAGAAGATCCACCTTCAATTAGTGAAGGATGTGGAGGAAGAGTTACAGACTACCGGATTACAGATTTTGGTGAATTTATGAGGGAAAACAGATTAACTCCTTTTCTAGACCCCAGATATAAAATCGATGGAAGTCTTGAGGTCCCTTTGGAACGAGCAAAAGATCAGTTAGAAAAACATACCCGTTACTGGCCTATGATCATTTCACAAACCACCATTTTTAACATGCAAGCGGTAGTTCCATTAGCCAGTGTTATTGTGAAAGAATCTCTGACAGAAGAAGATGTGTTAAACTGTCAAAAAACAATATACAACTTAGTTGATATGGAAAGAAAAAATGATCCTCTACCTATTTCCACAGTTGGTACAAGAGGAAAGGGCCCTAAAAGAGATGAACAATACCGTATCATGTGGAATGAATTAGAAACCCTTGTCAGAGCCCATATCAACAACTCAGAGAAACATCAAAGAGTCTTGGAATGTCTGATGGCATGCAGGAGCAAACCCCCAGAAGAGGAAGAACGAAAGAAACGAGGAAGAAAGAGGGAAGACAAAGAGGACAAGTCAGAGAAAGCAGTGAAAGATTATGAACAGGAAAAGTCTTGGCAAGACTCAGAGAGATTAAAAGGAATCTTAGAGCGTGGAAAAGAAGAATTGGCTGAAGCTGAGATTATAAAAGATTCGCCTGATTCCCCAGAACCTCCAAACAAAAAACCCCTTGTTGAAATGGATGAAACTCCACAAGTGGAAAAATCAAAAGGGCCAGTGTCGTTATTATCCTTGTGGAGTAATAGAATCAATACTGCCAATTCCAGAAAACATCAGGAATTTGCTGGACGTTTGAACTCTGTTAATAACAGAGCTGAACTATATCAACATCTTAAAGAGGAAAATGGGATGGAGACAACAGAAAATGGAAAAGCCAGCCGGCAGTGA
Amino sequence
MKIFSESHKTVFVVDHCPYMAESCRQHVEFDMLVKNRTQGIIPLAPISKSLWTCSVESSMEYCRIMYDIFPFKKLVNFIVSDSGAHVLNSWTQEDQNLQELMAALAAVGPPNPRADPECCSILHGLVAAVETLCKITEYQHEARTLLMENAERVGNRGRIICITNAKSDSHVRMLEDCVQETIHEHNKLAANSDHLMQIQKCELVLIHTYPVGEDSLVSDRSKKELSPVLTSEVHSVRAGRHLATKLNILVQQHFDLASTTITNIPMKEEQHANTSANYDVELLHHKDAHVDFLKSGDSHLGGGSREGSFKETITLKWCTPRTNNIELHYCTGAYRISPVDVNSRPSSCLTNFLLNGRSVLLEQPRKSGSKVISHMLSSHGGEIFLHVLSSSRSILEDPPSISEGCGGRVTDYRITDFGEFMRENRLTPFLDPRYKIDGSLEVPLERAKDQLEKHTRYWPMIISQTTIFNMQAVVPLASVIVKESLTEEDVLNCQKTIYNLVDMERKNDPLPISTVGTRGKGPKRDEQYRIMWNELETLVRAHINNSEKHQRVLECLMACRSKPPEEEERKKRGRKREDKEDKSEKAVKDYEQEKSWQDSERLKGILERGKEELAEAEIIKDSPDSPEPPNKKPLVEMDETPQVEKSKGPVSLLSLWSNRINTANSRKHQEFAGRLNSVNNRAELYQHLKEENGMETTENGKASRQ*