ENST00000598963.3 HSFX2
Information
- Transcript ID
- ENST00000598963.3
- Genome
- hg38
- Position
- chrX:149,592,512-149,595,314
- Strand
- -
- CDS length
- 1,272
- Amino acid length
- 424
- Gene symbol
- HSFX2
- Gene type
- protein-coding
- Gene description
- heat shock transcription factor family, X-linked 2
- Gene Entrez Gene ID
- 100130086
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 |
|---|---|---|
| 2 | 149,592,512 | 149,593,299 |
| 1 | 149,594,137 | 149,595,314 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 149,592,592 | 149,593,299 |
| 1 | CDS | 149,594,137 | 149,594,700 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chrX | 148,674,172 | 148,676,974 | Link |
CDS sequence
ATGGAGGACAAGCGATCATTGAGTATGGCTCGCTGTGAAGAAAGAAATTCGAGGGGACAGGATCATGGCTTGGAAAGGGTGCCTTTCCCTCCCCAGTTGCAGTCAGAGACCTACCTTCACCCAGCAGATCCTTCCCCTGCCTGGGACGACCCGGGGTCCACTGGGAGCCCTAACTTGAGGCTGCTGACAGAAGAAATCGCTTTCCAACCTCTGGCCGAGGAAGCTTCGTTCAGAAGGCCGCACCCTGACGGTGACGTCCCGCCCCAGGGAGAAGATAATCTCCTCTCCCTCCCCTTTCCACAGAAACTGTGGAGACTGGTCAGCAGCAACCAGTTTTCGTCCATCTGGTGGGATGACAGTGGGGCTTGTAGAGTGATCAATCAAAAACTCTTTGAAAAGGAGATTCTCAAAAGGGACGTCGCACACAAAGTGTTTGCCACAACTTCGATAAAGAGCTTCTTCCGCCAGCTAAACTTGTATGGCTTCCGAAAACGGCGTCAATGCACTTTCAGGACCTTCACCCGCATTTTCTCCGCAAAAAGGCTGGTCTCCATCTTGAATAAGTTAGAGTTCTACTGCCATCCTTACTTTCAAAGAGACTCCCCTCACCTCCTCGTGAGGATGAAGAGAAGAGTGGGTGTCAAGTCTGCACCAAGACATCAGGAGGAGGACAAGCCAGAAGCTGCTGGATCCTGTCTGGCACCAGCAGACACTGAGCAACAAGATCACACGTCTCCGAATGAGAATGACCAGGTCACACCGCAACACCGGGAACCGGCCGGTCCCAACACCCAAATCAGGAGTGGCTCTGCTCCACCAGCAACTCCTGTGATGGTGCCTGATTCCGCCGTGGCGAGTGACAACAGTCCAGTGACCCAGCCGGCCGGCGAGTGGTCAGAGGGCAGCCAGGCTCACGTCACTCCGGTGGCCGCTGTCCCTGGGCCTGCAGCGCTGCCCTTCCTCTATGTCCCTGGATCTCCCACTCAGATGAATTCTTACGGGCCTGTGGTGGCCCTTCCCACAGCGTCCCGTAGTACCCTTGCCATGGACACCACAGGACTTCCTGCACCTGGCATGCTGCCCTTTTGCCATCTCTGGGTACCGGTGACCCTAGTGGCTGCTGGGGCTGCACAGCCTGCTGCCTCCATGGTCATGTTCCCCCATCTCCCAGCTCTGCACCACCATTGCCCCCACAGCCACCGCACGTCACAGTACATGCCAGCTAGCGATGGGCCCCAGGCGTACCCAGACTACGCAGACCAGAGCACATAG
Amino sequence
MEDKRSLSMARCEERNSRGQDHGLERVPFPPQLQSETYLHPADPSPAWDDPGSTGSPNLRLLTEEIAFQPLAEEASFRRPHPDGDVPPQGEDNLLSLPFPQKLWRLVSSNQFSSIWWDDSGACRVINQKLFEKEILKRDVAHKVFATTSIKSFFRQLNLYGFRKRRQCTFRTFTRIFSAKRLVSILNKLEFYCHPYFQRDSPHLLVRMKRRVGVKSAPRHQEEDKPEAAGSCLAPADTEQQDHTSPNENDQVTPQHREPAGPNTQIRSGSAPPATPVMVPDSAVASDNSPVTQPAGEWSEGSQAHVTPVAAVPGPAALPFLYVPGSPTQMNSYGPVVALPTASRSTLAMDTTGLPAPGMLPFCHLWVPVTLVAAGAAQPAASMVMFPHLPALHHHCPHSHRTSQYMPASDGPQAYPDYADQST*