ENST00000449592.7 TMEM120B
Information
- Transcript ID
- ENST00000449592.7
- Genome
- hg19
- Position
- chr12:122,150,658-122,219,974
- Strand
- +
- CDS length
- 1,020
- Amino acid length
- 340
- Gene symbol
- TMEM120B
- Gene type
- protein-coding
- Gene description
- transmembrane protein 120B
- Gene Entrez Gene ID
- 144404
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 |
|---|---|---|
| 1 | 122,150,658 | 122,150,870 |
| 2 | 122,181,535 | 122,181,653 |
| 3 | 122,186,232 | 122,186,348 |
| 4 | 122,188,286 | 122,188,345 |
| 5 | 122,190,034 | 122,190,129 |
| 6 | 122,199,555 | 122,199,644 |
| 7 | 122,208,813 | 122,208,878 |
| 8 | 122,209,394 | 122,209,455 |
| 9 | 122,211,327 | 122,211,419 |
| 10 | 122,212,564 | 122,212,628 |
| 11 | 122,212,968 | 122,213,036 |
| 12 | 122,213,515 | 122,219,974 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 122,150,802 | 122,150,870 |
| 2 | CDS | 122,181,535 | 122,181,653 |
| 3 | CDS | 122,186,232 | 122,186,348 |
| 4 | CDS | 122,188,286 | 122,188,345 |
| 5 | CDS | 122,190,034 | 122,190,129 |
| 6 | CDS | 122,199,555 | 122,199,644 |
| 7 | CDS | 122,208,813 | 122,208,878 |
| 8 | CDS | 122,209,394 | 122,209,455 |
| 9 | CDS | 122,211,327 | 122,211,419 |
| 10 | CDS | 122,212,564 | 122,212,628 |
| 11 | CDS | 122,212,968 | 122,213,036 |
| 12 | CDS | 122,213,515 | 122,213,628 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr12 | 121,712,752 | 121,782,068 | Link |
CDS sequence
ATGTCCGGGCAGCTGGAGCGTTGCGAGCGCGAATGGCACGAGCTGGAGGGAGAATTTCAAGAACTGCAGGAGACGCACAGGATCTACAAGCAGAAGCTGGAGGAGCTGGCTGCGCTGCAGACGCTGTGTAGCAGTTCCATCAGTAAGCAGAAGAAGCACCTCAAGGACTTGAAGCTTACACTCCAGAGGTGCAAACGCCATGCCAGTCGGGAGGAGGCGGAGCTCGTTCAGCAGATGGCAGCGAACATCAAGGAGCGGCAGGACGTCTTCTTCGACATGGAGGCCTACCTGCCCAAGAAGAACGGGCTCTACTTGAACCTGGTCCTCGGCAATGTGAACGTGACCCTCCTCAGCAACCAGGCCAAGTTCGCCTACAAGGACGAATATGAGAAGTTCAAGCTCTACCTGACCATCATCCTGCTCCTGGGTGCCGTGGCATGTCGATTTGTCCTTCACTACAGGGTGACTGACGAAGTCTTCAACTTCCTGCTGGTGTGGTATTACTGCACCCTGACCATTCGGGAGAGCATTCTCATCAGCAACGGCTCAAGAATTAAAGGCTGGTGGGTGTCTCACCACTACGTCTCCACATTCCTGTCCGGAGTGATGCTGACCTGGCCTAATGGACCCATTTATCAGAAGTTTCGCAACCAGTTCTTAGCATTTTCCATTTTTCAGAGCTGCGTCCAGTTCCTGCAATATTATTACCAGAGGGGCTGCCTCTACCGGCTGCGGGCCCTGGGGGAGAGGAACCACCTGGATCTCACAGTGGAAGGGTTCCAGTCCTGGATGTGGCGGGGCCTCACCTTTCTCCTGCCCTTCCTCTTCTGTGGCCATTTCTGGCAGCTCTACAATGCCGTCACGCTGTTTGAGCTCTCCAGCCACGAGGAATGCAGAGAATGGCAGGTGTTCGTACTGGCGTTCACCTTCCTCATCCTCTTCCTCGGCAACTTCCTGACCACGCTCAAAGTCGTGCATGCCAAGCTCCAGAAGAACAGAGGCAAGACAAAGCAGCCGTGA
Amino sequence
MSGQLERCEREWHELEGEFQELQETHRIYKQKLEELAALQTLCSSSISKQKKHLKDLKLTLQRCKRHASREEAELVQQMAANIKERQDVFFDMEAYLPKKNGLYLNLVLGNVNVTLLSNQAKFAYKDEYEKFKLYLTIILLLGAVACRFVLHYRVTDEVFNFLLVWYYCTLTIRESILISNGSRIKGWWVSHHYVSTFLSGVMLTWPNGPIYQKFRNQFLAFSIFQSCVQFLQYYYQRGCLYRLRALGERNHLDLTVEGFQSWMWRGLTFLLPFLFCGHFWQLYNAVTLFELSSHEECREWQVFVLAFTFLILFLGNFLTTLKVVHAKLQKNRGKTKQP*