ENST00000373294.8 TBX22
Information
- Transcript ID
- ENST00000373294.8
- Genome
- hg19
- Position
- chrX:79,277,741-79,287,268
- Strand
- +
- CDS length
- 1,563
- Amino acid length
- 521
- Gene symbol
- TBX22
- Gene type
- protein-coding
- Gene description
- T-box transcription factor 22
- Gene Entrez Gene ID
- 50945
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 | 79,277,741 | 79,277,943 |
| 2 | 79,278,559 | 79,278,739 |
| 3 | 79,279,562 | 79,279,663 |
| 4 | 79,281,102 | 79,281,276 |
| 5 | 79,282,203 | 79,282,367 |
| 6 | 79,282,755 | 79,282,819 |
| 7 | 79,283,490 | 79,283,575 |
| 8 | 79,285,997 | 79,287,268 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 79,277,769 | 79,277,943 |
| 2 | CDS | 79,278,559 | 79,278,739 |
| 3 | CDS | 79,279,562 | 79,279,663 |
| 4 | CDS | 79,281,102 | 79,281,276 |
| 5 | CDS | 79,282,203 | 79,282,367 |
| 6 | CDS | 79,282,755 | 79,282,819 |
| 7 | CDS | 79,283,490 | 79,283,575 |
| 8 | CDS | 79,285,997 | 79,286,610 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chrX | 80,022,242 | 80,031,769 | Link |
CDS sequence
ATGGCTCTGAGCTCTCGGGCGCGTGCCTTCTCCGTGGAAGCCTTGGTGGGGAGACCCAGCAAAAGAAAACTCCAAGACCCAATACAGGCGGAGCAGCCTGAGCTGCGGGAGAAAAAGGGCGGAGAGGAAGAGGAGGAGAGAAGGAGCAGCGCTGCAGGGAAGAGCGAGCCGCTTGAAAAACAACCTAAGACAGAGCCCTCAACATCTGCTTCCTCTGGCTGCGGCAGCGACAGCGGCTACGGCAACAGCTCTGAAAGTCTGGAAGAGAAAGATATTCAAATGGAGCTTCAAGGATCTGAACTGTGGAAAAGATTCCATGACATCGGGACTGAGATGATCATTACTAAAGCGGGCAGGCGGATGTTCCCCTCTGTTCGGGTCAAGGTGAAAGGGTTGGATCCAGGGAAGCAGTACCATGTGGCCATCGATGTGGTGCCGGTGGATTCCAAACGCTATAGGTACGTCTATCACAGCTCACAGTGGATGGTAGCTGGGAATACAGACCATTTGTGCATCATTCCTAGATTCTATGTTCACCCGGACTCACCCTGCTCGGGAGAGACCTGGATGCGGCAGATCATCAGCTTTGATCGCATGAAACTCACCAACAATGAGATGGATGACAAAGGCCACATCATTCTGCAATCCATGCATAAGTACAAACCCCGAGTGCACGTGATAGAGCAAGGCAGCAGTGTTGACCTGTCCCAGATTCAGTCCTTGCCCACTGAAGGTGTTAAAACATTCTCCTTTAAAGAAACTGAGTTCACCACAGTAACGGCTTACCAAAACCAACAGATTACGAAACTAAAAATAGAAAGAAATCCTTTTGCTAAAGGATTTAGAGATACTGGAAGAAACAGGGGTGTATTGGATGGGCTTTTAGAGACCTACCCATGGAGGCCTTCTTTCACTCTCGATTTTAAAACCTTTGGCGCAGACACACAAAGTGGAAGCAGTGGCTCATCTCCAGTGACCTCTAGTGGAGGGGCCCCCTCTCCTTTGAACTCCTTACTTTCTCCACTTTGCTTTTCACCTATGTTTCATTTACCTACAAGCTCCCTTGGAATGCCCTGTCCAGAGGCATACCTGCCCAATGTCAACCTGCCTCTATGCTACAAGATTTGTCCAACTAATTTTTGGCAACAGCAACCTCTTGTTTTACCGGCTCCTGAAAGACTAGCAAGCAGCAACAGTTCTCAGTCTTTAGCCCCACTCATGATGGAAGTGCCTATGTTATCTTCCCTGGGGGTCACCAATTCAAAAAGCGGTTCATCTGAAGACTCCAGTGATCAGTATCTACAAGCACCTAATTCTACCAATCAAATGTTATATGGATTACAGTCACCTGGAAATATTTTTCTGCCAAACTCCATCACCCCAGAAGCACTTAGTTGCTCCTTTCATCCTTCCTATGACTTTTATAGATACAATTTCTCTATGCCATCTAGACTGATAAGTGGTTCCAACCATCTTAAAGTGAATGACGACAGTCAAGTTTCTTTTGGAGAAGGCAAATGTAATCATGTTCATTGGTATCCAGCAATTAACCATTACCTTTAG
Amino sequence
MALSSRARAFSVEALVGRPSKRKLQDPIQAEQPELREKKGGEEEEERRSSAAGKSEPLEKQPKTEPSTSASSGCGSDSGYGNSSESLEEKDIQMELQGSELWKRFHDIGTEMIITKAGRRMFPSVRVKVKGLDPGKQYHVAIDVVPVDSKRYRYVYHSSQWMVAGNTDHLCIIPRFYVHPDSPCSGETWMRQIISFDRMKLTNNEMDDKGHIILQSMHKYKPRVHVIEQGSSVDLSQIQSLPTEGVKTFSFKETEFTTVTAYQNQQITKLKIERNPFAKGFRDTGRNRGVLDGLLETYPWRPSFTLDFKTFGADTQSGSSGSSPVTSSGGAPSPLNSLLSPLCFSPMFHLPTSSLGMPCPEAYLPNVNLPLCYKICPTNFWQQQPLVLPAPERLASSNSSQSLAPLMMEVPMLSSLGVTNSKSGSSEDSSDQYLQAPNSTNQMLYGLQSPGNIFLPNSITPEALSCSFHPSYDFYRYNFSMPSRLISGSNHLKVNDDSQVSFGEGKCNHVHWYPAINHYL*