ENST00000299162.10 FOXN4
Information
- Transcript ID
- ENST00000299162.10
- Genome
- hg19
- Position
- chr12:109,715,783-109,747,089
- Strand
- -
- CDS length
- 1,554
- Amino acid length
- 518
- Gene symbol
- FOXN4
- Gene type
- protein-coding
- Gene description
- forkhead box N4
- Gene Entrez Gene ID
- 121643
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 |
---|---|---|
10 | 109,715,783 | 109,717,735 |
9 | 109,719,212 | 109,719,604 |
8 | 109,723,109 | 109,723,316 |
7 | 109,724,453 | 109,724,549 |
6 | 109,725,202 | 109,725,329 |
5 | 109,725,649 | 109,725,759 |
4 | 109,725,861 | 109,725,985 |
3 | 109,727,946 | 109,728,091 |
2 | 109,746,041 | 109,746,129 |
1 | 109,746,924 | 109,747,089 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 109,717,476 | 109,717,735 |
9 | CDS | 109,719,212 | 109,719,604 |
8 | CDS | 109,723,109 | 109,723,316 |
7 | CDS | 109,724,453 | 109,724,549 |
6 | CDS | 109,725,202 | 109,725,329 |
5 | CDS | 109,725,649 | 109,725,759 |
4 | CDS | 109,725,861 | 109,725,985 |
3 | CDS | 109,727,946 | 109,728,091 |
2 | CDS | 109,746,041 | 109,746,126 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr12 | 109,277,978 | 109,309,284 | Link |
CDS sequence
ATGATAGAAAGTGACACCTCATCCATAATGTCAGGAATTATTCGAAACTCAGGGCAAAATCACCACCCCTCTCCACAGGAATACAGGCTTCTAGCCACCACCAGCGATGATGACCTTCCCGGGGACCTGCAGTCGCTGTCGTGGCTCACGGCGGTGGATGTGCCTCGGCTGCAGCAGATGGCAAGTGGCCGCGTGGACCTGGGTGGCCCCTGCGTGCCACATCCACACCCAGGTGCCTTGGCTGGGGTGGCCGACCTGCATGTGGGAGCCACTCCAAGTCCCCTTCTCCATGGCCCAGCAGGCATGGCCCCCCGAGGCATGCCAGGTCTGGGCCCCATAACTGGCCACAGAGACAGCATGAGCCAGTTCCCCGTGGGGGGCCAGCCCTCATCTGGCCTGCAGGACCCGCCGCATCTGTACTCACCTGCCACCCAACCACAGTTCCCGCTCCCCCCGGGTGCCCAGCAGTGCCCTCCTGTGGGCCTCTATGGCCCCCCATTTGGGGTGCGGCCCCCCTACCCCCAGCCCCACGTGGCTGTGCATTCATCTCAAGAACTGCACCCCAAACACTACCCCAAGCCCATCTACTCGTACAGCTGTCTGATCGCCATGGCCCTGAAGAACAGCAAGACAGGCAGCCTGCCTGTGAGCGAGATCTACAGCTTCATGAAGGAGCACTTCCCCTACTTCAAGACGGCCCCCGACGGGTGGAAGAACTCGGTGCGGCACAACCTGTCTCTGAACAAGTGCTTCGAGAAGGTGGAGAACAAGATGAGCGGCTCCTCCCGCAAGGGCTGCCTGTGGGCTCTGAACCTGGCCCGCATCGACAAGATGGAGGAGGAGATGCACAAGTGGAAGAGGAAGGACCTGGCTGCCATCCACCGGAGTATGGCCAACCCTGAGGAGTTGGACAAGCTGATCTCCGACCGGCCTGAAAGCTGCCGGCGCCCCGGCAAACCGGGGGAACCAGAGGCCCCCGTGCTGACTCACGCCACCACAGTGGCCGTGGCGCATGGCTGCCTGGCTGTCTCCCAGCTCCCACCCCAGCCACTGATGACCCTGTCCCTGCAGTCAGTCCCCCTGCACCACCAGGTCCAGCCCCAGGCACATCTTGCTCCAGACTCTCCAGCACCAGCCCAGACCCCGCCACTGCACGCCCTGCCGGACCTCAGCCCCAGCCCGCTCCCCCACCCCGCCATGGGAAGGGCTCCTGTAGACTTCATCAACATCAGCACCGACATGAACACTGAGGTGGATGCCCTCGACCCGAGCATCATGGACTTCGCTCTGCAGGGGAACCTGTGGGAGGAGATGAAGGATGAGGGATTCAGCTTGGACACACTGGGCGCCTTTGCAGACTCCCCGCTTGGCTGTGACCTGGGGGCCTCAGGCCTAACCCCTGCCTCGGGTGGCAGCGACCAGTCCTTCCCAGACTTGCAGGTGACGGGTCTCTACACAGCGTACTCCACTCCGGACAGTGTGGCTGCATCGGGCACCAGCTCCTCCTCCCAGTACCTGGGTGCACAGGGGAACAAGCCTATAGCCCTGCTTTGA
Amino sequence
MIESDTSSIMSGIIRNSGQNHHPSPQEYRLLATTSDDDLPGDLQSLSWLTAVDVPRLQQMASGRVDLGGPCVPHPHPGALAGVADLHVGATPSPLLHGPAGMAPRGMPGLGPITGHRDSMSQFPVGGQPSSGLQDPPHLYSPATQPQFPLPPGAQQCPPVGLYGPPFGVRPPYPQPHVAVHSSQELHPKHYPKPIYSYSCLIAMALKNSKTGSLPVSEIYSFMKEHFPYFKTAPDGWKNSVRHNLSLNKCFEKVENKMSGSSRKGCLWALNLARIDKMEEEMHKWKRKDLAAIHRSMANPEELDKLISDRPESCRRPGKPGEPEAPVLTHATTVAVAHGCLAVSQLPPQPLMTLSLQSVPLHHQVQPQAHLAPDSPAPAQTPPLHALPDLSPSPLPHPAMGRAPVDFINISTDMNTEVDALDPSIMDFALQGNLWEEMKDEGFSLDTLGAFADSPLGCDLGASGLTPASGGSDQSFPDLQVTGLYTAYSTPDSVAASGTSSSSQYLGAQGNKPIALL*