ENST00000174618.5 MNT
Information
- Transcript ID
- ENST00000174618.5
- Genome
- hg19
- Position
- chr17:2,287,367-2,304,354
- Strand
- -
- CDS length
- 1,749
- Amino acid length
- 583
- Gene symbol
- MNT
- Gene type
- protein-coding
- Gene description
- MAX network transcriptional repressor
- Gene Entrez Gene ID
- 4335
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 |
|---|---|---|
| 6 | 2,287,367 | 2,290,943 |
| 5 | 2,291,151 | 2,291,343 |
| 4 | 2,297,337 | 2,297,448 |
| 3 | 2,297,599 | 2,297,640 |
| 2 | 2,298,169 | 2,298,748 |
| 1 | 2,303,934 | 2,304,354 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 6 | CDS | 2,290,195 | 2,290,943 |
| 5 | CDS | 2,291,151 | 2,291,343 |
| 4 | CDS | 2,297,337 | 2,297,448 |
| 3 | CDS | 2,297,599 | 2,297,640 |
| 2 | CDS | 2,298,169 | 2,298,748 |
| 1 | CDS | 2,303,934 | 2,304,006 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr17 | 2,384,073 | 2,401,060 | Link |
CDS sequence
ATGAGCATAGAGACGCTACTGGAGGCGGCCCGCTTCCTGGAATGGCAAGCGCAGCAACAACAGAGAGCACGTGAGGAGCAGGAGCGGCTTCGCTTGGAGCAGGAGCGAGAGCAGGAACAGAAGAAGGCCAATAGCCTGGCCAGGCTGGCACATACCCTTCCTGTGGAGGAACCCCGCATGGAGGCGCCACCCCTGCCTCTGTCTCCACCGGCTCCCCCGCCGGCACCCCCACCACCACTTGCCACCCCTGCCCCACTGACTGTCATCCCTATCCCTGTGGTGACCAACTCCCCTCAGCCTCTACCCCCACCCCCACCCTTGCCCGCGGCAGCCCAGCCTCTGCCCCTGGCGCCTCGTCAGCCGGCCCTGGTTGGCGCCCCCGGACTCAGCATTAAGGAGCCTGCCCCCCTGCCCAGCAGGCCGCAGGTGCCCACCCCTGCTCCCCTACTGCCGGACTCGAAGGCCACCATTCCACCCAATGGCAGCCCCAAGCCTTTGCAGCCCCTCCCCACGCCTGTCCTGACCATAGCGCCACACCCTGGAGTCCAGCCTCAGCTGGCCCCCCAGCAGCCGCCCCCACCCACGCTGGGGACCCTGAAGTTGGCACCAGCTGAAGAAGTCAAATCCAGTGAACAGAAGAAGAGGCCCGGGGGGATCGGAACCAGAGAAGTCCACAACAAATTGGAGAAGAACAGGAGGGCCCATCTGAAAGAGTGCTTTGAGACCCTGAAGCGGAACATCCCCAACGTGGATGACAAGAAGACGTCCAATCTGAGCGTGCTGCGGACGGCGCTGCGGTACATCCAGTCCCTGAAGAGGAAGGAGAAGGAATATGAGCATGAAATGGAGCGGCTGGCACGTGAGAAGATTGCCACGCAGCAGCGGCTGGCAGAGCTCAAGCACGAGCTGAGCCAGTGGATGGACGTACTGGAGATTGACCGCGTGCTGCGGCAGACGGGCCAGCCCGAGGATGACCAGGCCTCCACCTCCACCGCCTCTGAGGGTGAGGACAACATAGACGAGGATATGGAGGAGGACCGGGCGGGCCTGGGCCCACCTAAGCTGAGCCATCGTCCCCAGCCGGAGCTGCTGAAGTCCACCCTGCCACCCCCCAGCACCACCCCTGCGCCTCTGCCTCCACACCCACACCCTCACCCCCACTCCGTGGCCCTACCTCCTGCCCACCTCCCCGTGCAGCAGCAGCAGCCACAGCAGAAGACCCCTCTGCCAGCCCCTCCTCCCCCACCGGCTGCCCCTGCCCAGACACTGGTGCCAGCTCCAGCCCATCTGGTGGCGACGGCTGGGGGTGGCTCCACGGTCATCGCCCACACAGCCACCACTCACGCTTCAGTCATCCAGACTGTGAACCACGTTCTGCAGGGGCCAGGCGGCAAGCACATCGCCCACATCGCCCCCTCGGCCCCCAGCCCTGCGGTGCAACTGGCGCCTGCCACACCCCCCATTGGGCACATCACTGTGCACCCTGCCACCCTCAACCATGTGGCCCACCTGGGCTCCCAGCTGCCCTTGTACCCGCAGCCCGTGGCAGTGAGCCACATCGCCCACACCCTCTCGCACCAGCAAGTCAACGGCACGGCCGGCCTGGGGCCCCCGGCTACTGTCATGGCAAAGCCGGCCGTGGGGGCTCAGGTGGTGCACCACCCCCAGCTGGTGGGCCAGACCGTGCTCAACCCTGTGACCATGGTCACCATGCCCTCCTTCCCAGTCAGCACACTCAAGCTGGCTTGA
Amino sequence
MSIETLLEAARFLEWQAQQQQRAREEQERLRLEQEREQEQKKANSLARLAHTLPVEEPRMEAPPLPLSPPAPPPAPPPPLATPAPLTVIPIPVVTNSPQPLPPPPPLPAAAQPLPLAPRQPALVGAPGLSIKEPAPLPSRPQVPTPAPLLPDSKATIPPNGSPKPLQPLPTPVLTIAPHPGVQPQLAPQQPPPPTLGTLKLAPAEEVKSSEQKKRPGGIGTREVHNKLEKNRRAHLKECFETLKRNIPNVDDKKTSNLSVLRTALRYIQSLKRKEKEYEHEMERLAREKIATQQRLAELKHELSQWMDVLEIDRVLRQTGQPEDDQASTSTASEGEDNIDEDMEEDRAGLGPPKLSHRPQPELLKSTLPPPSTTPAPLPPHPHPHPHSVALPPAHLPVQQQQPQQKTPLPAPPPPPAAPAQTLVPAPAHLVATAGGGSTVIAHTATTHASVIQTVNHVLQGPGGKHIAHIAPSAPSPAVQLAPATPPIGHITVHPATLNHVAHLGSQLPLYPQPVAVSHIAHTLSHQQVNGTAGLGPPATVMAKPAVGAQVVHHPQLVGQTVLNPVTMVTMPSFPVSTLKLA*