ENST00000261191.12 INTS13
Information
- Transcript ID
- ENST00000261191.12
- Genome
- hg19
- Position
- chr12:27,058,114-27,090,914
- 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
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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 |
---|---|---|
17 | 27,058,114 | 27,058,469 |
16 | 27,059,235 | 27,059,370 |
15 | 27,064,111 | 27,064,250 |
14 | 27,066,390 | 27,066,620 |
13 | 27,066,907 | 27,067,061 |
12 | 27,067,341 | 27,067,511 |
11 | 27,068,935 | 27,069,113 |
10 | 27,070,285 | 27,070,374 |
9 | 27,070,577 | 27,070,666 |
8 | 27,075,549 | 27,075,633 |
7 | 27,077,288 | 27,077,416 |
6 | 27,078,694 | 27,078,784 |
5 | 27,081,138 | 27,081,218 |
4 | 27,081,636 | 27,081,838 |
3 | 27,087,489 | 27,087,563 |
2 | 27,089,512 | 27,089,747 |
1 | 27,090,729 | 27,090,914 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
17 | CDS | 27,058,430 | 27,058,469 |
16 | CDS | 27,059,235 | 27,059,370 |
15 | CDS | 27,064,111 | 27,064,250 |
14 | CDS | 27,066,390 | 27,066,620 |
13 | CDS | 27,066,907 | 27,067,061 |
12 | CDS | 27,067,341 | 27,067,511 |
11 | CDS | 27,068,935 | 27,069,113 |
10 | CDS | 27,070,285 | 27,070,374 |
9 | CDS | 27,070,577 | 27,070,666 |
8 | CDS | 27,075,549 | 27,075,633 |
7 | CDS | 27,077,288 | 27,077,416 |
6 | CDS | 27,078,694 | 27,078,784 |
5 | CDS | 27,081,138 | 27,081,218 |
4 | CDS | 27,081,636 | 27,081,838 |
3 | CDS | 27,087,489 | 27,087,563 |
2 | CDS | 27,089,512 | 27,089,736 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr12 | 26,905,181 | 26,937,981 | Link |
CDS sequence
ATGAAGATTTTTTCTGAATCTCATAAAACAGTGTTTGTTGTGGATCACTGCCCTTATATGGCAGAATCTTGCAGGCAGCATGTCGAGTTTGATATGCTGGTGAAGAATAGAACCCAAGGAATCATTCCTTTGGCCCCCATATCTAAATCATTGTGGACTTGCTCAGTAGAATCTTCCATGGAATATTGTAGAATAATGTATGATATATTTCCTTTCAAAAAGCTGGTGAATTTTATTGTGAGTGACTCTGGAGCACATGTTTTAAATTCTTGGACTCAAGAAGACCAAAATTTACAGGAGCTAATGGCAGCATTAGCCGCTGTTGGGCCTCCTAATCCTCGGGCAGATCCAGAGTGCTGCAGTATTCTGCATGGCCTTGTTGCAGCAGTGGAAACTCTCTGCAAAATTACTGAATACCAACATGAGGCTCGTACTCTACTCATGGAGAATGCAGAACGTGTTGGAAATAGAGGACGAATAATCTGTATTACTAATGCAAAAAGTGATAGTCATGTGCGAATGCTTGAAGACTGTGTCCAGGAAACGATTCATGAACATAACAAGCTTGCTGCAAATTCAGATCATCTCATGCAGATTCAAAAATGTGAGTTGGTCTTGATCCACACCTACCCAGTTGGTGAAGACAGCCTTGTATCTGATCGTTCTAAAAAAGAGTTGTCCCCGGTTTTAACCAGTGAAGTTCATAGTGTTCGTGCAGGACGGCATCTTGCTACCAAATTGAATATTTTAGTACAGCAACATTTTGACTTGGCTTCAACTACTATTACAAATATTCCAATGAAGGAAGAACAGCATGCTAACACATCTGCCAATTATGATGTGGAGCTACTTCATCACAAAGATGCACATGTAGATTTCCTGAAAAGTGGTGATTCGCATCTAGGTGGCGGCAGTCGAGAAGGCTCGTTTAAAGAAACAATAACATTAAAGTGGTGTACACCAAGGACAAATAACATTGAATTACACTATTGTACTGGAGCTTATCGGATTTCACCTGTAGATGTAAATAGTAGACCTTCCTCCTGCCTTACTAATTTTCTTCTAAATGGTCGTTCTGTTTTATTGGAACAACCACGAAAGTCAGGTTCTAAAGTCATTAGTCATATGCTTAGTAGCCATGGAGGAGAGATTTTTTTGCACGTCCTTAGCAGTTCTCGATCCATTCTAGAAGATCCACCTTCAATTAGTGAAGGATGTGGAGGAAGAGTTACAGACTACCGGATTACAGATTTTGGTGAATTTATGAGGGAAAACAGATTAACTCCTTTTCTAGACCCCAGATATAAAATCGATGGAAGTCTTGAGGTCCCTTTGGAACGAGCAAAAGATCAGTTAGAAAAACATACCCGTTACTGGCCTATGATCATTTCACAAACCACCATTTTTAACATGCAAGCGGTAGTTCCATTAGCCAGTGTTATTGTGAAAGAATCTCTGACAGAAGAAGATGTGTTAAACTGTCAAAAAACAATATACAACTTAGTTGATATGGAAAGAAAAAATGATCCTCTACCTATTTCCACAGTTGGTACAAGAGGAAAGGGCCCTAAAAGAGATGAACAATACCGTATCATGTGGAATGAATTAGAAACCCTTGTCAGAGCCCATATCAACAACTCAGAGAAACATCAAAGAGTCTTGGAATGTCTGATGGCATGCAGGAGCAAACCCCCAGAAGAGGAAGAACGAAAGAAACGAGGAAGAAAGAGGGAAGACAAAGAGGACAAGTCAGAGAAAGCAGTGAAAGATTATGAACAGGAAAAGTCTTGGCAAGACTCAGAGAGATTAAAAGGAATCTTAGAGCGTGGAAAAGAAGAATTGGCTGAAGCTGAGATTATAAAAGATTCGCCTGATTCCCCAGAACCTCCAAACAAAAAACCCCTTGTTGAAATGGATGAAACTCCACAAGTGGAAAAATCAAAAGGGCCAGTGTCGTTATTATCCTTGTGGAGTAATAGAATCAATACTGCCAATTCCAGAAAACATCAGGAATTTGCTGGACGTTTGAACTCTGTTAATAACAGAGCTGAACTATATCAACATCTTAAAGAGGAAAATGGGATGGAGACAACAGAAAATGGAAAAGCCAGCCGGCAGTGA
Amino sequence
MKIFSESHKTVFVVDHCPYMAESCRQHVEFDMLVKNRTQGIIPLAPISKSLWTCSVESSMEYCRIMYDIFPFKKLVNFIVSDSGAHVLNSWTQEDQNLQELMAALAAVGPPNPRADPECCSILHGLVAAVETLCKITEYQHEARTLLMENAERVGNRGRIICITNAKSDSHVRMLEDCVQETIHEHNKLAANSDHLMQIQKCELVLIHTYPVGEDSLVSDRSKKELSPVLTSEVHSVRAGRHLATKLNILVQQHFDLASTTITNIPMKEEQHANTSANYDVELLHHKDAHVDFLKSGDSHLGGGSREGSFKETITLKWCTPRTNNIELHYCTGAYRISPVDVNSRPSSCLTNFLLNGRSVLLEQPRKSGSKVISHMLSSHGGEIFLHVLSSSRSILEDPPSISEGCGGRVTDYRITDFGEFMRENRLTPFLDPRYKIDGSLEVPLERAKDQLEKHTRYWPMIISQTTIFNMQAVVPLASVIVKESLTEEDVLNCQKTIYNLVDMERKNDPLPISTVGTRGKGPKRDEQYRIMWNELETLVRAHINNSEKHQRVLECLMACRSKPPEEEERKKRGRKREDKEDKSEKAVKDYEQEKSWQDSERLKGILERGKEELAEAEIIKDSPDSPEPPNKKPLVEMDETPQVEKSKGPVSLLSLWSNRINTANSRKHQEFAGRLNSVNNRAELYQHLKEENGMETTENGKASRQ*