ENST00000433935.6 ZMYND15
Information
- Transcript ID
- ENST00000433935.6
- Genome
- hg38
- Position
- chr17:4,739,833-4,746,113
- Strand
- +
- CDS length
- 2,229
- Amino acid length
- 743
- Gene symbol
- ZMYND15
- Gene type
- protein-coding
- Gene description
- zinc finger MYND-type containing 15
- Gene Entrez Gene ID
- 84225
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 | 4,739,833 | 4,740,050 |
| 2 | 4,740,519 | 4,741,140 |
| 3 | 4,741,582 | 4,741,816 |
| 4 | 4,741,915 | 4,742,070 |
| 5 | 4,742,331 | 4,742,491 |
| 6 | 4,743,303 | 4,743,455 |
| 7 | 4,743,767 | 4,743,847 |
| 8 | 4,743,991 | 4,744,107 |
| 9 | 4,744,190 | 4,744,278 |
| 10 | 4,744,369 | 4,744,467 |
| 11 | 4,744,625 | 4,744,778 |
| 12 | 4,744,870 | 4,744,928 |
| 13 | 4,745,215 | 4,745,375 |
| 14 | 4,745,819 | 4,746,113 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 4,740,549 | 4,741,140 |
| 3 | CDS | 4,741,582 | 4,741,816 |
| 4 | CDS | 4,741,915 | 4,742,070 |
| 5 | CDS | 4,742,331 | 4,742,491 |
| 6 | CDS | 4,743,303 | 4,743,455 |
| 7 | CDS | 4,743,767 | 4,743,847 |
| 8 | CDS | 4,743,991 | 4,744,107 |
| 9 | CDS | 4,744,190 | 4,744,278 |
| 10 | CDS | 4,744,369 | 4,744,467 |
| 11 | CDS | 4,744,625 | 4,744,778 |
| 12 | CDS | 4,744,870 | 4,744,928 |
| 13 | CDS | 4,745,215 | 4,745,375 |
| 14 | CDS | 4,745,819 | 4,745,990 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr17 | 4,643,128 | 4,649,408 | Link |
CDS sequence
ATGGAGTTTGTGTCTGGATACCGGGATGAGTTCCTTGATTTCACTGCCCTTCTCTTCGGCTGGTTCCGAAAGTTTGTGGCAGAGCGTGGAGCTGTAGGGACTAGCCTTGAGGGCCGCTGCCGGCAGCTGGAGGCCCAGATCAGAAGGCTACCCCAGGACCCTGCCCTTTGGGTGCTCCATGTCCTGCCCAACCATAGTGTGGGCATCAGCCTGGGGCAAGGGGCAGAACCAGGTCCTGGACCAGGCCTGGGGACTGCCTGGCTCCTGGGAGACAACCCTCCACTCCACCTGCGAGACCTGAGCCCCTACATCAGCTTTGTCAGCCTAGAGGATGGGGAGGAAGGGGAGGAGGAAGAGGAGGAAGATGAAGAAGAAGAGAAGAGAGAGGACGGGGGTGCAGGCAGCACAGAGAAGGTGGAACCAGAGGAGGACCGGGAGCTAGCCCCTACCAGCAGGGAGTCCCCCCAGGAAACAAACCCTCCAGGAGAGTCAGAGGAGGCTGCCCGGGAGGCAGGAGGTGGCAAGGATGGCTGCCGAGAGGACAGGGTGGAGAACGAAACAAGACCCCAGAAGAGGAAGGGACAGAGGAGTGAGGCTGCCCCCCTGCACGTTTCCTGTCTCTTACTTGTGACGGATGAGCATGGCACCATCTTGGGCATTGATCTGCTAGTGGATGGAGCCCAGGGAACCGCAAGCTGGGGCTCAGGGACCAAGGACCTGGCTCCTTGGGCCTATGCTCTCCTCTGTCACAGCATGGCCTGTCCCATGGGCTCTGGGGATCCCCGAAAGCCCCGACAGCTTACTGTGGGAGATGCCCGGCTGCATCGAGAGCTGGAGAGCTTGGTCCCAAGGCTAGGTGTGAAGTTAGCCAAAACCCCAATGCGGACATGGGGTCCCCGGCCAGGCTTCACCTTTGCTTCCCTTCGTGCTCGAACCTGCCATGTGTGTCACAGGCACAGCTTTGAAGCGAAGCTGACACCTTGCCCCCAGTGTAGTGCTGTCTTGTATTGTGGAGAGGCTTGTCTCCGGGCTGACTGGCAGCGGTGCCCAGATGATGTGAGTCACCGATTTTGGTGCCCAAGGCTTGCAGCCTTCATGGAGCGGGCAGGAGAACTGGCAACCCTGCCTTTTACCTACACCGCAGAGGTGACCAGTGAAACCTTCAACAAAGAGGCCTTCCTGGCCTCTCGGGGCCTCACTCGTGGCTATTGGACCCAGCTCAGCATGCTGATTCCAGGCCCGGGCTTCTCCAGACACCCCCGAGGCAACACGCCATCCCTCAGCCTTCTTCGCGGTGGAGACCCCTACCAGCTTCTCCAGGGAGACGGGACTGCCCTGATGCCTCCTGTGCCCCCACATCCACCCCGGGGTGTTTTTGGCTCATGGCAGGATTACTACACATGGCGGGGCCTCAGCTTGGACTCCCCCATAGCCGTGCTTCTCACCTACCCGCTGACCGTGTACTACGTCATCACCCACCTGGTGCCCCAGTCCTTCCCTGAGCTCAACATCCAAAACAAACAGTCACTGAAGATCCACGTGGTGGAGGCCGGGAAGGAGTTTGACCTTGTCATGGTGTTTTGGGAGCTTTTGGTCCTGCTCCCCCATGTGGCCCTGGAGCTGCAGTTTGTAGGTGATGGCCTGCCCCCCGAAAGCGACGAGCAGCATTTTACCCTGCAGAGGGACAGCCTGGAGGTGTCTGTCCGGCCTGGTTCCGGCATATCAGCACGGCCCAGCTCTGGCACTAAGGAGAAAGGGGGCCGCAGGGACCTGCAGATCAAGGTGTCAGCAAGGCCCTACCACCTGTTCCAGGGGCCCAAGCCTGACCTGGTTATTGGATTTAACTCCGGGTTTGCTCTCAAGGATACGTGGCTGAGGTCTCTGCCCCGGTTACAGTCCCTCCGAGTGCCAGCCTTCTTCACCGAGAGCAGCGAGTACAGCTGTGTGATGGACGGCCAGACCATGGCGGTGGCCACTGGAGGGGGCACCAGCCCTCCCCAGCCCAACCCCTTCCGCTCCCCCTTTCGCCTCAGAGCGGCCGACAACTGCATGTCCTGGTACTGCAATGCCTTCATCTTCCACCTGGTTTACAAGCCTGCTCAAGGGAGCGGGGCCCGCCCGGCGCCCGGGCCCCCACCCCCATCCCCAACTCCCTCTGCTCCTCCTGCCCCCACCCGAAGGCGCCGAGGAGAAAAGAAACCTGGGCGGGGGGCCCGCCGGCGGAAATGA
Amino sequence
MEFVSGYRDEFLDFTALLFGWFRKFVAERGAVGTSLEGRCRQLEAQIRRLPQDPALWVLHVLPNHSVGISLGQGAEPGPGPGLGTAWLLGDNPPLHLRDLSPYISFVSLEDGEEGEEEEEEDEEEEKREDGGAGSTEKVEPEEDRELAPTSRESPQETNPPGESEEAAREAGGGKDGCREDRVENETRPQKRKGQRSEAAPLHVSCLLLVTDEHGTILGIDLLVDGAQGTASWGSGTKDLAPWAYALLCHSMACPMGSGDPRKPRQLTVGDARLHRELESLVPRLGVKLAKTPMRTWGPRPGFTFASLRARTCHVCHRHSFEAKLTPCPQCSAVLYCGEACLRADWQRCPDDVSHRFWCPRLAAFMERAGELATLPFTYTAEVTSETFNKEAFLASRGLTRGYWTQLSMLIPGPGFSRHPRGNTPSLSLLRGGDPYQLLQGDGTALMPPVPPHPPRGVFGSWQDYYTWRGLSLDSPIAVLLTYPLTVYYVITHLVPQSFPELNIQNKQSLKIHVVEAGKEFDLVMVFWELLVLLPHVALELQFVGDGLPPESDEQHFTLQRDSLEVSVRPGSGISARPSSGTKEKGGRRDLQIKVSARPYHLFQGPKPDLVIGFNSGFALKDTWLRSLPRLQSLRVPAFFTESSEYSCVMDGQTMAVATGGGTSPPQPNPFRSPFRLRAADNCMSWYCNAFIFHLVYKPAQGSGARPAPGPPPPSPTPSAPPAPTRRRRGEKKPGRGARRRK*