ENST00000248901.11 CYTH4
Information
- Transcript ID
- ENST00000248901.11
- Genome
- hg19
- Position
- chr22:37,678,549-37,711,382
- Strand
- +
- CDS length
- 1,185
- Amino acid length
- 395
- Gene symbol
- CYTH4
- Gene type
- protein-coding
- Gene description
- cytohesin 4
- Gene Entrez Gene ID
- 27128
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 |
---|---|---|
1 | 37,678,549 | 37,678,629 |
2 | 37,688,662 | 37,688,744 |
3 | 37,690,701 | 37,690,765 |
4 | 37,692,040 | 37,692,106 |
5 | 37,693,605 | 37,693,723 |
6 | 37,695,267 | 37,695,347 |
7 | 37,696,948 | 37,697,060 |
8 | 37,699,295 | 37,699,443 |
9 | 37,705,253 | 37,705,364 |
10 | 37,707,029 | 37,707,105 |
11 | 37,707,497 | 37,707,568 |
12 | 37,708,061 | 37,708,215 |
13 | 37,709,480 | 37,711,382 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 37,678,611 | 37,678,629 |
2 | CDS | 37,688,662 | 37,688,744 |
3 | CDS | 37,690,701 | 37,690,765 |
4 | CDS | 37,692,040 | 37,692,106 |
5 | CDS | 37,693,605 | 37,693,723 |
6 | CDS | 37,695,267 | 37,695,347 |
7 | CDS | 37,696,948 | 37,697,060 |
8 | CDS | 37,699,295 | 37,699,443 |
9 | CDS | 37,705,253 | 37,705,364 |
10 | CDS | 37,707,029 | 37,707,105 |
11 | CDS | 37,707,497 | 37,707,568 |
12 | CDS | 37,708,061 | 37,708,215 |
13 | CDS | 37,709,480 | 37,709,552 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr22 | 37,282,508 | 37,315,341 | Link |
CDS sequence
ATGGACCTGTGCCACCCAGAGCCCGCGGAGCTGAGCAGCGGGGAGACGGAAGAGTTACAGAGGATCAAGTGGCACCGAAAGCAGCTCCTGGAGGACATCCAGAAGCTGAAGGATGAGATTGCAGATGTGTTTGCCCAAATCGACTGCTTCGAGAGTGCGGAGGAGAGCCGGATGGCCCAGAAGGAGAAGGAGCTGTGTATTGGGCGCAAGAAGTTCAACATGGACCCCGCCAAGGGTATCCAGTATTTCATTGAGCACAAGCTGCTGACCCCTGACGTCCAGGACATTGCACGGTTCCTGTATAAAGGCGAGGGCCTCAACAAGACAGCCATTGGTACCTACCTGGGGGAGAGGGATCCCATCAACCTGCAGGTCCTCCAGGCCTTCGTGGACTGCCACGAGTTCGCCAACCTCAACCTCGTCCAGGCCCTCAGGCAGTTCCTGTGGAGCTTCCGGCTGCCGGGCGAGGCCCAGAAGATAGACCGGATGATGGAGGCCTTTGCCACTCGATACTGCCTCTGCAACCCAGGCGTCTTCCAGTCCACAGACACCTGCTACGTGTTGTCCTTCTCCATCATCATGCTCAACACCAGCCTCCACAATCCCAACGTCCGGGACAGGCCGCCTTTTGAGCGCTTTGTGTCCATGAACCGCGGCATCAACAATGGTAGCGACCTGCCCGAGGACCAGCTGCGGAACCTCTTCGACAGCATCAAGAGTGAGCCATTCTCCATCCCTGAGGACGACGGCAATGACCTCACTCACACCTTCTTCAATCCAGACCGGGAGGGTTGGCTGCTCAAGCTAGGGGGCCGCGTGAAGACGTGGAAACGGCGCTGGTTCATCCTGACCGACAACTGCCTCTACTACTTCGAGTTCACCACTGACAAGGAGCCACGGGGAATTATACCTCTTGAGAACCTCTCGGTGCAGAAGGTGGATGACCCCAAGAAGCCATTCTGCCTGGAGCTCTACAACCCTAGCTGCCGAGGCCAGAAAATCAAGGCCTGCAAGACCGATGGCGACGGCAGGGTGGTGGAGGGCAAGCACGAATCGTACCGCATCTCAGCCACCAGTGCCGAGGAACGTGACCAGTGGATCGAGTCCATCCGAGCCAGCATCACCCGTGTCCCCTTCTACGACCTGGTCTCTACTCGGAAGAAGAAGATTGCCAGCAAGCAGTGA
Amino sequence
MDLCHPEPAELSSGETEELQRIKWHRKQLLEDIQKLKDEIADVFAQIDCFESAEESRMAQKEKELCIGRKKFNMDPAKGIQYFIEHKLLTPDVQDIARFLYKGEGLNKTAIGTYLGERDPINLQVLQAFVDCHEFANLNLVQALRQFLWSFRLPGEAQKIDRMMEAFATRYCLCNPGVFQSTDTCYVLSFSIIMLNTSLHNPNVRDRPPFERFVSMNRGINNGSDLPEDQLRNLFDSIKSEPFSIPEDDGNDLTHTFFNPDREGWLLKLGGRVKTWKRRWFILTDNCLYYFEFTTDKEPRGIIPLENLSVQKVDDPKKPFCLELYNPSCRGQKIKACKTDGDGRVVEGKHESYRISATSAEERDQWIESIRASITRVPFYDLVSTRKKKIASKQ*