ENST00000283916.11 TMPRSS11D
Information
- Transcript ID
- ENST00000283916.11
- Genome
- hg19
- Position
- chr4:68,686,594-68,749,720
- Strand
- -
- CDS length
- 1,257
- Amino acid length
- 419
- Gene symbol
- TMPRSS11D
- Gene type
- protein-coding
- Gene description
- transmembrane serine protease 11D
- Gene Entrez Gene ID
- 9407
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 |
|---|---|---|
| 10 | 68,686,594 | 68,688,216 |
| 9 | 68,691,450 | 68,691,592 |
| 8 | 68,692,979 | 68,693,238 |
| 7 | 68,698,922 | 68,699,099 |
| 6 | 68,700,801 | 68,700,839 |
| 5 | 68,703,890 | 68,704,047 |
| 4 | 68,708,276 | 68,708,343 |
| 3 | 68,719,786 | 68,719,904 |
| 2 | 68,725,275 | 68,725,396 |
| 1 | 68,749,644 | 68,749,720 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 10 | CDS | 68,688,055 | 68,688,216 |
| 9 | CDS | 68,691,450 | 68,691,592 |
| 8 | CDS | 68,692,979 | 68,693,238 |
| 7 | CDS | 68,698,922 | 68,699,099 |
| 6 | CDS | 68,700,801 | 68,700,839 |
| 5 | CDS | 68,703,890 | 68,704,047 |
| 4 | CDS | 68,708,276 | 68,708,343 |
| 3 | CDS | 68,719,786 | 68,719,904 |
| 2 | CDS | 68,725,275 | 68,725,396 |
| 1 | CDS | 68,749,644 | 68,749,651 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr4 | 67,820,876 | 67,884,002 | Link |
CDS sequence
ATGTATAGGCCAGCACGTGTAACTTCGACTTCAAGATTTCTGAATCCATATGTAGTATGTTTCATTGTCGTCGCAGGGGTAGTGATCCTGGCAGTCACCATAGCTCTACTTGTTTACTTTTTAGCTTTTGATCAAAAATCTTACTTTTATAGGAGCAGTTTTCAACTCCTAAATGTTGAATATAATAGTCAGTTAAATTCACCAGCTACACAGGAATACAGGACTTTGAGTGGAAGAATTGAATCTCTGATTACTAAAACATTCAAAGAATCAAATTTAAGAAATCAGTTCATCAGAGCTCATGTTGCCAAACTGAGGCAAGATGGTAGTGGTGTGAGAGCGGATGTTGTCATGAAATTTCAATTCACTAGAAATAACAATGGAGCATCAATGAAAAGCAGAATTGAGTCTGTTTTACGACAAATGCTGAATAACTCTGGAAACCTGGAAATAAACCCTTCAACTGAGATAACATCACTTACTGACCAGGCTGCAGCAAATTGGCTTATTAATGAATGTGGGGCCGGTCCAGACCTAATAACATTGTCTGAGCAGAGAATCCTTGGAGGCACTGAGGCTGAGGAGGGAAGCTGGCCGTGGCAAGTCAGTCTGCGGCTCAATAATGCCCACCACTGTGGAGGCAGCCTGATCAATAACATGTGGATCCTGACAGCAGCTCACTGCTTCAGAAGCAACTCTAATCCTCGTGACTGGATTGCCACGTCTGGTATTTCCACAACATTTCCTAAACTAAGAATGAGAGTAAGAAATATTTTAATTCATAACAATTATAAATCTGCAACTCATGAAAATGACATTGCACTTGTGAGACTTGAGAACAGTGTCACCTTTACCAAAGATATCCATAGTGTGTGTCTCCCAGCTGCTACCCAGAATATTCCACCTGGCTCTACTGCTTATGTAACAGGATGGGGCGCTCAAGAATATGCTGGCCACACAGTTCCAGAGCTAAGGCAAGGACAGGTCAGAATAATAAGTAATGATGTATGTAATGCACCACATAGTTATAATGGAGCCATCTTGTCTGGAATGCTGTGTGCTGGAGTACCTCAAGGTGGAGTGGACGCATGTCAGGGTGACTCTGGTGGCCCACTAGTACAAGAAGACTCACGGCGGCTTTGGTTTATTGTGGGGATAGTAAGCTGGGGAGATCAGTGTGGCCTGCCGGATAAGCCAGGAGTGTATACTCGAGTGACAGCCTACCTTGACTGGATTAGGCAACAAACTGGGATCTAG
Amino sequence
MYRPARVTSTSRFLNPYVVCFIVVAGVVILAVTIALLVYFLAFDQKSYFYRSSFQLLNVEYNSQLNSPATQEYRTLSGRIESLITKTFKESNLRNQFIRAHVAKLRQDGSGVRADVVMKFQFTRNNNGASMKSRIESVLRQMLNNSGNLEINPSTEITSLTDQAAANWLINECGAGPDLITLSEQRILGGTEAEEGSWPWQVSLRLNNAHHCGGSLINNMWILTAAHCFRSNSNPRDWIATSGISTTFPKLRMRVRNILIHNNYKSATHENDIALVRLENSVTFTKDIHSVCLPAATQNIPPGSTAYVTGWGAQEYAGHTVPELRQGQVRIISNDVCNAPHSYNGAILSGMLCAGVPQGGVDACQGDSGGPLVQEDSRRLWFIVGIVSWGDQCGLPDKPGVYTRVTAYLDWIRQQTGI*