ENST00000299162.10 FOXN4
Information
- Transcript ID
- ENST00000299162.10
- Genome
- hg38
- Position
- chr12:109,277,978-109,309,284
- 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 | 109,277,978 | 109,279,930 |
9 | 109,281,407 | 109,281,799 |
8 | 109,285,304 | 109,285,511 |
7 | 109,286,648 | 109,286,744 |
6 | 109,287,397 | 109,287,524 |
5 | 109,287,844 | 109,287,954 |
4 | 109,288,056 | 109,288,180 |
3 | 109,290,141 | 109,290,286 |
2 | 109,308,236 | 109,308,324 |
1 | 109,309,119 | 109,309,284 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 109,279,671 | 109,279,930 |
9 | CDS | 109,281,407 | 109,281,799 |
8 | CDS | 109,285,304 | 109,285,511 |
7 | CDS | 109,286,648 | 109,286,744 |
6 | CDS | 109,287,397 | 109,287,524 |
5 | CDS | 109,287,844 | 109,287,954 |
4 | CDS | 109,288,056 | 109,288,180 |
3 | CDS | 109,290,141 | 109,290,286 |
2 | CDS | 109,308,236 | 109,308,321 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr12 | 109,715,783 | 109,747,089 | Link |
CDS sequence
ATGATAGAAAGTGACACCTCATCCATAATGTCAGGAATTATTCGAAACTCAGGGCAAAATCACCACCCCTCTCCACAGGAATACAGGCTTCTAGCCACCACCAGCGATGATGACCTTCCCGGGGACCTGCAGTCGCTGTCGTGGCTCACGGCGGTGGATGTGCCTCGGCTGCAGCAGATGGCAAGTGGCCGCGTGGACCTGGGTGGCCCCTGCGTGCCACATCCACACCCAGGTGCCTTGGCTGGGGTGGCCGACCTGCATGTGGGAGCCACTCCAAGTCCCCTTCTCCATGGCCCAGCAGGCATGGCCCCCCGAGGCATGCCAGGTCTGGGCCCCATAACTGGCCACAGAGACAGCATGAGCCAGTTCCCCGTGGGGGGCCAGCCCTCATCTGGCCTGCAGGACCCGCCGCATCTGTACTCACCTGCCACCCAACCACAGTTCCCGCTCCCCCCGGGTGCCCAGCAGTGCCCTCCTGTGGGCCTCTATGGCCCCCCATTTGGGGTGCGGCCCCCCTACCCCCAGCCCCACGTGGCTGTGCATTCATCTCAAGAACTGCACCCCAAACACTACCCCAAGCCCATCTACTCGTACAGCTGTCTGATCGCCATGGCCCTGAAGAACAGCAAGACAGGCAGCCTGCCTGTGAGCGAGATCTACAGCTTCATGAAGGAGCACTTCCCCTACTTCAAGACGGCCCCCGACGGGTGGAAGAACTCGGTGCGGCACAACCTGTCTCTGAACAAGTGCTTCGAGAAGGTGGAGAACAAGATGAGCGGCTCCTCCCGCAAGGGCTGCCTGTGGGCTCTGAACCTGGCCCGCATCGACAAGATGGAGGAGGAGATGCACAAGTGGAAGAGGAAGGACCTGGCTGCCATCCACCGGAGTATGGCCAACCCTGAGGAGTTGGACAAGCTGATCTCCGACCGGCCTGAAAGCTGCCGGCGCCCCGGCAAACCGGGGGAACCAGAGGCCCCCGTGCTGACTCACGCCACCACAGTGGCCGTGGCGCATGGCTGCCTGGCTGTCTCCCAGCTCCCACCCCAGCCACTGATGACCCTGTCCCTGCAGTCAGTCCCCCTGCACCACCAGGTCCAGCCCCAGGCACATCTTGCTCCAGACTCTCCAGCACCAGCCCAGACCCCGCCACTGCACGCCCTGCCGGACCTCAGCCCCAGCCCGCTCCCCCACCCCGCCATGGGAAGGGCTCCTGTAGACTTCATCAACATCAGCACCGACATGAACACTGAGGTGGATGCCCTCGACCCGAGCATCATGGACTTCGCTCTGCAGGGGAACCTGTGGGAGGAGATGAAGGATGAGGGATTCAGCTTGGACACACTGGGCGCCTTTGCAGACTCCCCGCTTGGCTGTGACCTGGGGGCCTCAGGCCTAACCCCTGCCTCGGGTGGCAGCGACCAGTCCTTCCCAGACTTGCAGGTGACGGGTCTCTACACAGCGTACTCCACTCCGGACAGTGTGGCTGCATCGGGCACCAGCTCCTCCTCCCAGTACCTGGGTGCACAGGGGAACAAGCCTATAGCCCTGCTTTGA
Amino sequence
MIESDTSSIMSGIIRNSGQNHHPSPQEYRLLATTSDDDLPGDLQSLSWLTAVDVPRLQQMASGRVDLGGPCVPHPHPGALAGVADLHVGATPSPLLHGPAGMAPRGMPGLGPITGHRDSMSQFPVGGQPSSGLQDPPHLYSPATQPQFPLPPGAQQCPPVGLYGPPFGVRPPYPQPHVAVHSSQELHPKHYPKPIYSYSCLIAMALKNSKTGSLPVSEIYSFMKEHFPYFKTAPDGWKNSVRHNLSLNKCFEKVENKMSGSSRKGCLWALNLARIDKMEEEMHKWKRKDLAAIHRSMANPEELDKLISDRPESCRRPGKPGEPEAPVLTHATTVAVAHGCLAVSQLPPQPLMTLSLQSVPLHHQVQPQAHLAPDSPAPAQTPPLHALPDLSPSPLPHPAMGRAPVDFINISTDMNTEVDALDPSIMDFALQGNLWEEMKDEGFSLDTLGAFADSPLGCDLGASGLTPASGGSDQSFPDLQVTGLYTAYSTPDSVAASGTSSSSQYLGAQGNKPIALL*