ENST00000680574.1 TCTN2
Information
- Transcript ID
- ENST00000680574.1
- Genome
- hg38
- Position
- chr12:123,671,110-123,707,997
- Strand
- +
- CDS length
- 1,959
- Amino acid length
- 653
- Gene symbol
- TCTN2
- Gene type
- protein-coding
- Gene description
- tectonic family member 2
- Gene Entrez Gene ID
- 79867
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 |
---|---|---|
1 | 123,671,110 | 123,671,322 |
2 | 123,671,507 | 123,671,614 |
3 | 123,672,056 | 123,672,132 |
4 | 123,673,615 | 123,673,810 |
5 | 123,679,189 | 123,679,289 |
6 | 123,686,836 | 123,687,035 |
7 | 123,688,051 | 123,688,177 |
8 | 123,690,533 | 123,690,674 |
9 | 123,692,658 | 123,692,723 |
10 | 123,695,220 | 123,695,297 |
11 | 123,696,415 | 123,696,495 |
12 | 123,697,087 | 123,697,198 |
13 | 123,699,704 | 123,699,810 |
14 | 123,704,532 | 123,704,688 |
15 | 123,706,726 | 123,706,851 |
16 | 123,706,985 | 123,707,073 |
17 | 123,707,604 | 123,707,997 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 123,671,241 | 123,671,322 |
2 | CDS | 123,671,507 | 123,671,614 |
3 | CDS | 123,672,056 | 123,672,132 |
4 | CDS | 123,673,615 | 123,673,810 |
5 | CDS | 123,679,189 | 123,679,289 |
6 | CDS | 123,686,836 | 123,687,035 |
7 | CDS | 123,688,051 | 123,688,177 |
8 | CDS | 123,690,533 | 123,690,674 |
9 | CDS | 123,692,658 | 123,692,723 |
10 | CDS | 123,695,220 | 123,695,297 |
11 | CDS | 123,696,415 | 123,696,495 |
12 | CDS | 123,697,087 | 123,697,198 |
13 | CDS | 123,699,704 | 123,699,810 |
14 | CDS | 123,704,532 | 123,704,688 |
15 | CDS | 123,706,726 | 123,706,851 |
16 | CDS | 123,706,985 | 123,707,073 |
17 | CDS | 123,707,604 | 123,707,713 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr12 | 124,155,657 | 124,192,544 | Link |
CDS sequence
ATGGGCTTCCAGCCTCCGGCCGCTCTTCTTTTGAGGCTTTTCCTTCTGCAGGGCATCCTGAGGCTTCTGTGGGGGGACCTGGCTTTCATCCCTCCTTTTATCCGAATGTCCGGCCCTGCGGTCAGCGCGTCCCTGGTCGGAGACACCGAGGGTGTGACCGTGTCCCTGGCAGTGCTGCAGGACGAGGCGGGAATATTGCCAATTCCGACGTGTGGAGTGCTGAACAATGAGACGGAAGACTGGAGCGTGACTGTGATCCCCGGTGCGAAGGTGTTGGAAGTGACAGTGAGGTGGAAGAGAGGTCTGGACTGGTGTTCCTCCAATGAGACAGATTCCTTCTCAGAGTCCCCCTGTATCCTCCAGACCCTTCTGGTTTCAGCATCTCATAATTCATCCTGTTCAGCACATCTACTCATTCAAGTGGAAATTTATGCCAACTCTTCTCTGACCCATAATGCCTCAGAGAACGTGACTGTCATTCCTAACCAGGTGTATCAGCCCCTTGGCCCTTGTCCTTGTAATTTAACAGCTGGAGCCTGTGATGTTCGCTGCTGCTGTGACCAGGAATGCTCATCAAATTTAACAACGCTGTTCAGACGGTCCTGCTTCACCGGCGTGTTTGGAGGAGACGTCAATCCTCCTTTTGATCAGCTCTGCTCTGCTGGGACGACGACACGTGGTGTCCCCGATTGGTTTCCCTTTCTGTGTGTGCAGTCCCCCCTTGCCAACACACCCTTCCTTGGTTACTTCTATCATGGTGCTGTTTCCCCCAAACAGGACTCTTCCTTTGAAGTATATGTGGATACTGACGCAAAAGACTTTGCAGACTTTGGTTACAAACAAGGAGATCCCATTATGACTGTAAAGAAGGCATATTTTACTATTCCGCAGGTGTCCCTGGCTGGGCAGTGTATGCAGAACGCCCCAGTGGCATTTCTTCACAATTTTGATGTTAAATGCGTTACTAATTTGGAACTATACCAAGAACGAGATGGTATTATCAATGCGAAGATAAAGAATGTTGCCTTAGGAGGCATAGTTACACCAAAAGTGATCTATGAGGAAGCAACTGACCTAGACAAATTCATCACCAATACAGGGATAATGACACAGAGATTTGTAGTAAAATTTTTAAGCTATAATAGTGGTAATGAAGAAGAATTATCTGGAAATCCAGGTTACCAACTTGGCAAGCCTGTCCGAGCTCTAAATATCAACAGGATGAATAATGTCACGACTTTACATCTTTGGCAATCGGCTGGAAGGGGTCTGTGTACATCAGCAACTTTCAAACCCATTTTATTTGGAGAAAATGTACTCTCTGGATGCCTGTTAGAAGTCGGGATTAATGAAAATTGTACTCAGCTCAGGGAGAATGCTGTTGAAAGACTTGATTCATTAATACAAGCGACTCACGTTGCAATGAGAGGCAACTCCGATTACGCTGATCTTAGTGATGGCTGGCTCGAAATAATACGTGTAGATGCCCCTGATCCAGGTGCAGACCCGCTGGCTAGCAGTGTGAACGGCATGTGCCTGGATATTCCTGCTCACCTGAGCATCCGCATCCTCATCTCGGATGCTGGCGCGGTGGAAGGGATTACTCAGCAGGAGATACTCGGTGTAGAGACAAGGTTCTCCTCAGTGAACTGGCAGTACCAGTGTGGGCTTACCTGTGAGCACAAGGCCGACCTTCTCCCTATCAGTGCATCCGTCCAGTTTATTAAAATTCCTGCACAGTTACCCCACCCCCTGACAAGATTCCAGATCAATTATACAGAGTATGACTGCAACAGAAATGAGGTGTGTTGGCCGCAGCTTCTATATCCATGGACTCAGTATTATCAAGGGGAGCTGCATTCTCAGTGTGTTGCTAAGGGCTTACTGTTGCTGTTGTTCCTCACATTGGCCTTGTTCCTCAGCAACCCCTGGACCAGAATATGCAAAGCCTATAGTTAG
Amino sequence
MGFQPPAALLLRLFLLQGILRLLWGDLAFIPPFIRMSGPAVSASLVGDTEGVTVSLAVLQDEAGILPIPTCGVLNNETEDWSVTVIPGAKVLEVTVRWKRGLDWCSSNETDSFSESPCILQTLLVSASHNSSCSAHLLIQVEIYANSSLTHNASENVTVIPNQVYQPLGPCPCNLTAGACDVRCCCDQECSSNLTTLFRRSCFTGVFGGDVNPPFDQLCSAGTTTRGVPDWFPFLCVQSPLANTPFLGYFYHGAVSPKQDSSFEVYVDTDAKDFADFGYKQGDPIMTVKKAYFTIPQVSLAGQCMQNAPVAFLHNFDVKCVTNLELYQERDGIINAKIKNVALGGIVTPKVIYEEATDLDKFITNTGIMTQRFVVKFLSYNSGNEEELSGNPGYQLGKPVRALNINRMNNVTTLHLWQSAGRGLCTSATFKPILFGENVLSGCLLEVGINENCTQLRENAVERLDSLIQATHVAMRGNSDYADLSDGWLEIIRVDAPDPGADPLASSVNGMCLDIPAHLSIRILISDAGAVEGITQQEILGVETRFSSVNWQYQCGLTCEHKADLLPISASVQFIKIPAQLPHPLTRFQINYTEYDCNRNEVCWPQLLYPWTQYYQGELHSQCVAKGLLLLLFLTLALFLSNPWTRICKAYS*