ENST00000473183.7 ESRP2
Information
- Transcript ID
- ENST00000473183.7
- Genome
- hg19
- Position
- chr16:68,262,936-68,270,030
- 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 | 68,262,936 | 68,264,218 |
| 14 | 68,264,292 | 68,264,457 |
| 13 | 68,264,744 | 68,264,930 |
| 12 | 68,265,081 | 68,265,279 |
| 11 | 68,265,385 | 68,265,597 |
| 10 | 68,265,705 | 68,266,006 |
| 9 | 68,266,149 | 68,266,191 |
| 8 | 68,266,274 | 68,266,406 |
| 7 | 68,266,480 | 68,266,590 |
| 6 | 68,266,664 | 68,266,718 |
| 5 | 68,267,230 | 68,267,328 |
| 4 | 68,267,671 | 68,267,785 |
| 3 | 68,267,897 | 68,268,010 |
| 2 | 68,269,537 | 68,269,665 |
| 1 | 68,269,751 | 68,270,030 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 15 | CDS | 68,264,129 | 68,264,218 |
| 14 | CDS | 68,264,292 | 68,264,457 |
| 13 | CDS | 68,264,744 | 68,264,930 |
| 12 | CDS | 68,265,081 | 68,265,279 |
| 11 | CDS | 68,265,385 | 68,265,597 |
| 10 | CDS | 68,265,705 | 68,266,006 |
| 9 | CDS | 68,266,149 | 68,266,191 |
| 8 | CDS | 68,266,274 | 68,266,406 |
| 7 | CDS | 68,266,480 | 68,266,590 |
| 6 | CDS | 68,266,664 | 68,266,718 |
| 5 | CDS | 68,267,230 | 68,267,328 |
| 4 | CDS | 68,267,671 | 68,267,785 |
| 3 | CDS | 68,267,897 | 68,268,010 |
| 2 | CDS | 68,269,537 | 68,269,665 |
| 1 | CDS | 68,269,751 | 68,269,948 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr16 | 68,229,033 | 68,236,127 | Link |
CDS sequence
ATGACTCCGCCGCCGCCGCCGCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGACCCCGCCGCGGACCCCTGCCCCTGGCCCGGATCACTGGTCGTCCTCTTCGGGGCTACGGCGGGTGCGCTGGGACGGGACCTGGGCTCGGACGAGACCGACTTAATCCTCCTAGTTTGGCAAGTGGTTGAGCCGCGGAGCCGCCAGGTGGGGACGCTGCACAAATCGCTGGTTCGTGCCGAGGCGGCCGCACTGAGTACGCAGTGCCGCGAGGCGAGCGGCCTGAGCGCCGACAGCCTGGCGCGGGCAGAGCCGCTGGACAAGGTGCTGCAGCAGTTCTCACAGCTGGTGAACGGGGATGTGGCTTTGCTGGGCGGGGGCCCCTACATGCTCTGCACTGATGGGCAGCAGCTATTGCGACAGGTCCTGCACCCCGAGGCCTCCAGGAAGAACCTGGTGCTCCCCGACATGTTCTTCTCCTTCTATGACCTCCGAAGAGAATTCCATATGCAGCATCCAAGCACCTGCCCTGCCAGGGACCTCACTGTGGCCACCATGGCACAGGGTTTAGGACTGGAGACAGATGCCACAGAGGATGACTTTGGGGTCTGGGAAGTCAAGACAATGGTAGCTGTTATCCTCCATCTACTCAAAGAGCCCAGCAGTCAATTGTTTTCGAAGCCCGAGGTGATAAAGCAGAAATACGAGACGGGGCCTTGCAGCAAGGCTGATGTGGTGGACAGTGAGACTGTGGTACGGGCTCGTGGGTTGCCGTGGCAGTCATCAGACCAGGACGTGGCTCGCTTCTTCAAAGGGCTCAACGTGGCCAGGGGTGGTGTAGCACTCTGCCTCAACGCCCAGGGCCGCAGAAATGGCGAGGCCCTCATCCGCTTTGTGGACAGCGAGCAGCGGGACCTAGCGCTGCAGAGACACAAGCACCACATGGGCGTCCGCTATATTGAGGTGTATAAAGCGACAGGGGAGGAGTTTGTAAAGATTGCAGGGGGCACATCACTAGAGGTGGCTCGTTTCTTGTCACGGGAAGACCAAGTGATCCTGCGGCTGCGGGGACTGCCCTTCTCGGCTGGGCCAACGGACGTGCTTGGCTTCCTGGGGCCAGAGTGCCCAGTGACTGGGGGTACCGAGGGGCTGCTCTTTGTGCGCCATCCTGATGGCCGGCCGACTGGTGATGCCTTCGCCCTCTTTGCTTGTGAGGAGCTGGCACAGGCTGCACTGCGCAGGCACAAGGGCATGCTGGGTAAGCGATACATTGAACTCTTCCGGAGCACTGCAGCCGAAGTGCAGCAGGTCTTGAACCGCTATGCATCCGGCCCACTCCTTCCTACACTGACTGCCCCACTGCTGCCCATCCCCTTCCCACTGGCACCTGGGACTGGGAGGGACTGTGTACGCCTCCGAGGCCTGCCCTACACGGCCACCATTGAAGACATCCTGAGCTTTCTGGGGGAGGCAGCAGCTGACATTCGGCCCCACGGTGTACACATGGTGCTCAACCAGCAGGGCCGGCCATCGGGCGATGCCTTCATTCAGATGACATCAGCAGAGCGAGCCCTAGCTGCTGCTCAGCGTTGCCATAAGAAGGTGATGAAGGAGCGCTACGTGGAGGTGGTCCCCTGTTCCACAGAGGAGATGAGCCGAGTGCTGATGGGGGGCACCTTGGGCCGCAGTGGCATGTCCCCTCCACCCTGCAAGCTGCCCTGCCTCTCACCACCTACCTACACCACCTTCCAAGCCACCCCAACGCTCATTCCCACGGAGACGGCAGCTCTATACCCCTCTTCAGCACTGCTCCCAGCTGCCAGGGTGCCTGCTGCCCCCACCCCTGTTGCCTACTATCCAGGGCCAGCCACTCAACTCTACCTGAACTACACAGCCTACTACCCAAGCCCCCCAGTCTCCCCCACCACTGTGGGCTACCTCACTACACCCACTGCTGCCCTGGCCTCTGCTCCCACCTCAGTGTTGTCCCAGTCAGGAGCCTTGGTCCGCATGCAGGGTGTCCCATACACGGCTGGTATGAAGGATCTGCTCAGCGTCTTCCAGGCCTACCAGCTACCCGCTGATGACTACACCAGTCTGATGCCTGTTGGTGACCCACCTCGCACTGTGTTACAAGCCCCCAAGGAATGGGTGTGTTTGTAG
Amino sequence
MTPPPPPPPPPGPDPAADPAADPCPWPGSLVVLFGATAGALGRDLGSDETDLILLVWQVVEPRSRQVGTLHKSLVRAEAAALSTQCREASGLSADSLARAEPLDKVLQQFSQLVNGDVALLGGGPYMLCTDGQQLLRQVLHPEASRKNLVLPDMFFSFYDLRREFHMQHPSTCPARDLTVATMAQGLGLETDATEDDFGVWEVKTMVAVILHLLKEPSSQLFSKPEVIKQKYETGPCSKADVVDSETVVRARGLPWQSSDQDVARFFKGLNVARGGVALCLNAQGRRNGEALIRFVDSEQRDLALQRHKHHMGVRYIEVYKATGEEFVKIAGGTSLEVARFLSREDQVILRLRGLPFSAGPTDVLGFLGPECPVTGGTEGLLFVRHPDGRPTGDAFALFACEELAQAALRRHKGMLGKRYIELFRSTAAEVQQVLNRYASGPLLPTLTAPLLPIPFPLAPGTGRDCVRLRGLPYTATIEDILSFLGEAAADIRPHGVHMVLNQQGRPSGDAFIQMTSAERALAAAQRCHKKVMKERYVEVVPCSTEEMSRVLMGGTLGRSGMSPPPCKLPCLSPPTYTTFQATPTLIPTETAALYPSSALLPAARVPAAPTPVAYYPGPATQLYLNYTAYYPSPPVSPTTVGYLTTPTAALASAPTSVLSQSGALVRMQGVPYTAGMKDLLSVFQAYQLPADDYTSLMPVGDPPRTVLQAPKEWVCL*