ENST00000473183.7 ESRP2
Information
- Transcript ID
- ENST00000473183.7
- Genome
- hg38
- Position
- chr16:68,229,033-68,236,127
- Strand
- -
- CDS length
- 2,154
- Amino acid length
- 718
- Gene symbol
- ESRP2
- Gene type
- protein-coding
- Gene description
- epithelial splicing regulatory protein 2
- Gene Entrez Gene ID
- 80004
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 |
|---|---|---|
| 15 | 68,229,033 | 68,230,315 |
| 14 | 68,230,389 | 68,230,554 |
| 13 | 68,230,841 | 68,231,027 |
| 12 | 68,231,178 | 68,231,376 |
| 11 | 68,231,482 | 68,231,694 |
| 10 | 68,231,802 | 68,232,103 |
| 9 | 68,232,246 | 68,232,288 |
| 8 | 68,232,371 | 68,232,503 |
| 7 | 68,232,577 | 68,232,687 |
| 6 | 68,232,761 | 68,232,815 |
| 5 | 68,233,327 | 68,233,425 |
| 4 | 68,233,768 | 68,233,882 |
| 3 | 68,233,994 | 68,234,107 |
| 2 | 68,235,634 | 68,235,762 |
| 1 | 68,235,848 | 68,236,127 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 15 | CDS | 68,230,226 | 68,230,315 |
| 14 | CDS | 68,230,389 | 68,230,554 |
| 13 | CDS | 68,230,841 | 68,231,027 |
| 12 | CDS | 68,231,178 | 68,231,376 |
| 11 | CDS | 68,231,482 | 68,231,694 |
| 10 | CDS | 68,231,802 | 68,232,103 |
| 9 | CDS | 68,232,246 | 68,232,288 |
| 8 | CDS | 68,232,371 | 68,232,503 |
| 7 | CDS | 68,232,577 | 68,232,687 |
| 6 | CDS | 68,232,761 | 68,232,815 |
| 5 | CDS | 68,233,327 | 68,233,425 |
| 4 | CDS | 68,233,768 | 68,233,882 |
| 3 | CDS | 68,233,994 | 68,234,107 |
| 2 | CDS | 68,235,634 | 68,235,762 |
| 1 | CDS | 68,235,848 | 68,236,045 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr16 | 68,262,936 | 68,270,030 | Link |
CDS sequence
ATGACTCCGCCGCCGCCGCCGCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGACCCCGCCGCGGACCCCTGCCCCTGGCCCGGATCACTGGTCGTCCTCTTCGGGGCTACGGCGGGTGCGCTGGGACGGGACCTGGGCTCGGACGAGACCGACTTAATCCTCCTAGTTTGGCAAGTGGTTGAGCCGCGGAGCCGCCAGGTGGGGACGCTGCACAAATCGCTGGTTCGTGCCGAGGCGGCCGCACTGAGTACGCAGTGCCGCGAGGCGAGCGGCCTGAGCGCCGACAGCCTGGCGCGGGCAGAGCCGCTGGACAAGGTGCTGCAGCAGTTCTCACAGCTGGTGAACGGGGATGTGGCTTTGCTGGGCGGGGGCCCCTACATGCTCTGCACTGATGGGCAGCAGCTATTGCGACAGGTCCTGCACCCCGAGGCCTCCAGGAAGAACCTGGTGCTCCCCGACATGTTCTTCTCCTTCTATGACCTCCGAAGAGAATTCCATATGCAGCATCCAAGCACCTGCCCTGCCAGGGACCTCACTGTGGCCACCATGGCACAGGGTTTAGGACTGGAGACAGATGCCACAGAGGATGACTTTGGGGTCTGGGAAGTCAAGACAATGGTAGCTGTTATCCTCCATCTACTCAAAGAGCCCAGCAGTCAATTGTTTTCGAAGCCCGAGGTGATAAAGCAGAAATACGAGACGGGGCCTTGCAGCAAGGCTGATGTGGTGGACAGTGAGACTGTGGTACGGGCTCGTGGGTTGCCGTGGCAGTCATCAGACCAGGACGTGGCTCGCTTCTTCAAAGGGCTCAACGTGGCCAGGGGTGGTGTAGCACTCTGCCTCAACGCCCAGGGCCGCAGAAATGGCGAGGCCCTCATCCGCTTTGTGGACAGCGAGCAGCGGGACCTAGCGCTGCAGAGACACAAGCACCACATGGGCGTCCGCTATATTGAGGTGTATAAAGCGACAGGGGAGGAGTTTGTAAAGATTGCAGGGGGCACATCACTAGAGGTGGCTCGTTTCTTGTCACGGGAAGACCAAGTGATCCTGCGGCTGCGGGGACTGCCCTTCTCGGCTGGGCCAACGGACGTGCTTGGCTTCCTGGGGCCAGAGTGCCCAGTGACTGGGGGTACCGAGGGGCTGCTCTTTGTGCGCCATCCTGATGGCCGGCCGACTGGTGATGCCTTCGCCCTCTTTGCTTGTGAGGAGCTGGCACAGGCTGCACTGCGCAGGCACAAGGGCATGCTGGGTAAGCGATACATTGAACTCTTCCGGAGCACTGCAGCCGAAGTGCAGCAGGTCTTGAACCGCTATGCATCCGGCCCACTCCTTCCTACACTGACTGCCCCACTGCTGCCCATCCCCTTCCCACTGGCACCTGGGACTGGGAGGGACTGTGTACGCCTCCGAGGCCTGCCCTACACGGCCACCATTGAAGACATCCTGAGCTTTCTGGGGGAGGCAGCAGCTGACATTCGGCCCCACGGTGTACACATGGTGCTCAACCAGCAGGGCCGGCCATCGGGCGATGCCTTCATTCAGATGACATCAGCAGAGCGAGCCCTAGCTGCTGCTCAGCGTTGCCATAAGAAGGTGATGAAGGAGCGCTACGTGGAGGTGGTCCCCTGTTCCACAGAGGAGATGAGCCGAGTGCTGATGGGGGGCACCTTGGGCCGCAGTGGCATGTCCCCTCCACCCTGCAAGCTGCCCTGCCTCTCACCACCTACCTACACCACCTTCCAAGCCACCCCAACGCTCATTCCCACGGAGACGGCAGCTCTATACCCCTCTTCAGCACTGCTCCCAGCTGCCAGGGTGCCTGCTGCCCCCACCCCTGTTGCCTACTATCCAGGGCCAGCCACTCAACTCTACCTGAACTACACAGCCTACTACCCAAGCCCCCCAGTCTCCCCCACCACTGTGGGCTACCTCACTACACCCACTGCTGCCCTGGCCTCTGCTCCCACCTCAGTGTTGTCCCAGTCAGGAGCCTTGGTCCGCATGCAGGGTGTCCCATACACGGCTGGTATGAAGGATCTGCTCAGCGTCTTCCAGGCCTACCAGCTACCCGCTGATGACTACACCAGTCTGATGCCTGTTGGTGACCCACCTCGCACTGTGTTACAAGCCCCCAAGGAATGGGTGTGTTTGTAG
Amino sequence
MTPPPPPPPPPGPDPAADPAADPCPWPGSLVVLFGATAGALGRDLGSDETDLILLVWQVVEPRSRQVGTLHKSLVRAEAAALSTQCREASGLSADSLARAEPLDKVLQQFSQLVNGDVALLGGGPYMLCTDGQQLLRQVLHPEASRKNLVLPDMFFSFYDLRREFHMQHPSTCPARDLTVATMAQGLGLETDATEDDFGVWEVKTMVAVILHLLKEPSSQLFSKPEVIKQKYETGPCSKADVVDSETVVRARGLPWQSSDQDVARFFKGLNVARGGVALCLNAQGRRNGEALIRFVDSEQRDLALQRHKHHMGVRYIEVYKATGEEFVKIAGGTSLEVARFLSREDQVILRLRGLPFSAGPTDVLGFLGPECPVTGGTEGLLFVRHPDGRPTGDAFALFACEELAQAALRRHKGMLGKRYIELFRSTAAEVQQVLNRYASGPLLPTLTAPLLPIPFPLAPGTGRDCVRLRGLPYTATIEDILSFLGEAAADIRPHGVHMVLNQQGRPSGDAFIQMTSAERALAAAQRCHKKVMKERYVEVVPCSTEEMSRVLMGGTLGRSGMSPPPCKLPCLSPPTYTTFQATPTLIPTETAALYPSSALLPAARVPAAPTPVAYYPGPATQLYLNYTAYYPSPPVSPTTVGYLTTPTAALASAPTSVLSQSGALVRMQGVPYTAGMKDLLSVFQAYQLPADDYTSLMPVGDPPRTVLQAPKEWVCL*