ENST00000466548.5 SLAIN1
Information
- Transcript ID
- ENST00000466548.5
- Genome
- hg19
- Position
- chr13:78,272,023-78,338,259
- Strand
- +
- CDS length
- 1,707
- Amino acid length
- 569
- Gene symbol
- SLAIN1
- Gene type
- protein-coding
- Gene description
- SLAIN motif family member 1
- Gene Entrez Gene ID
- 122060
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 | 78,272,023 | 78,272,338 |
2 | 78,272,405 | 78,272,674 |
3 | 78,293,667 | 78,293,806 |
4 | 78,318,418 | 78,318,567 |
5 | 78,320,649 | 78,320,990 |
6 | 78,327,338 | 78,327,493 |
7 | 78,334,963 | 78,335,245 |
8 | 78,337,280 | 78,338,259 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 78,272,049 | 78,272,338 |
2 | CDS | 78,272,405 | 78,272,674 |
3 | CDS | 78,293,667 | 78,293,806 |
4 | CDS | 78,318,418 | 78,318,567 |
5 | CDS | 78,320,649 | 78,320,990 |
6 | CDS | 78,327,338 | 78,327,493 |
7 | CDS | 78,334,963 | 78,335,245 |
8 | CDS | 78,337,280 | 78,337,355 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr13 | 77,697,888 | 77,764,124 | Link |
CDS sequence
ATGATGGCGGAGCAGGTGAAATGCGCCTCGGCAGGGGTCAGCTCTGGAGCGGGCTCCGGGCCGGTGGTGAACGCGGAGCTGGAGGTGAAGAAGCTGCAGGAGCTGGTGCGCAAGCTGGAGAAGCAGAACGAGCAGCTGCGGAGTCGAGCGGCCAGCGCGGCCGCCGCCCCGCACCTGCTGCTGCTGCCGCCGCCGCCGCCCGCCGCGCCGCCCCCCGCTGGCCTGCAGCCTTTGGGTCCTCGGAGCCCCCCGGCCGCCACGGCCACCGCCGCGGCCTCAGGGGGCCTGGGCCCCGCGTTCCCGGGCACCTTCTGCCTGCCTAGCCCCGCGCCCTCCCTGCTTTGCAGCCTGGCGCAGCCACCCGAGGCGCCCTTCGTCTACTTCAAGCCGGCAGCAGGCTTCTTCGGCGCGGGCGGTGGCGGGCCGGAGCCGGGGGGCGCGGGGACGCCGCCAGGGGCAGCTGCAGCGCCGCCCTCGCCGCCCCCCACGCTGCTGGACGAGGTGGAATTGCTGGATCTGGAGAGCGTAGCCGCCTGGCGGGACGAGGACGACTACACCTGGTTATACATTGGCTCTTCAAAGACGTTCACCTCATCAGAGAAATCCCTGACTCCTTTGCAGTGGTGTAGACATGTCCTAGATAACCCAACTCCTGAGATGGAAGCAGCGAGACGTTCCCTGTGCTTTAGACTGGAGCAAGGTTACACTTCCAGGGGCTCCCCACTCAGTCCCCAGTCATCTATCGACAGTGAGCTGAGTACTTCAGAATTGGAGGATGATTCTATCTCCATGGGATATAAATTACAGGACCTCACTGATGTTCAGATCATGGCTCGTCTGCAAGAAGAAAGTCTCAGGCAAGATTATGCTTCTACTTCAGCATCTGTATCAAGACATAGTTCCAGTGTGTCATTGAGTTCAGGAAAAAAAGGGACATGTAGTGATCAAGAATATGACCAATACAGTCTGGAGGATGAAGAGGAATTTGATCATTTGCCACCACCTCAGCCTCGTCTTCCAAGATGTTCCCCTTTCCAAAGAGGAATTCCCCATTCACAGACTTTCTCCAGCATTCGGGAGTGTAGGAGGAGCCCCAGTTCCCAGTATTTTCCTTCAAATAATTACCAGCAGCAACAGTATTATTCACCTCAAGCCCAAACTCCAGATCAGCAACCAAATAGGACCAATGGAGATAAGCTCCGAAGAAGTATGCCTAACCTAGCCCGGATGCCAAGTACAACTGCCATTAGTAGCAACATTAGTTCTCCGGTCACCGTGCGAAATAGTCAGAGTTTTGACTCAAGCTTGCATGGAGCTGGAAATGGAATTTCAAGAATACAATCTTGTATTCCATCACCGGGACAGCTTCAACACAGGGTCCACAGCGTGGGGCATTTCCCAGTGTCTATCCGACAGCCTCTTAAAGCCACAGCCTATGTGAGTCCAACCGTTCAAGGCAGCAGTAACATGCCTTTATCAAACGGCTTACAGCTGTATTCCAACACAGGAATCCCCACACCGAACAAAGCTGCAGCTTCTGGGATAATGGGTCGCAGTGCACTCCCAAGACCTTCGTTGGCAATAAATGGGAGTAACCTGCCTCGAAGCAAAATTGCACAACCTGTTAGAAGTTTTCTTCAGCCTCCAAAGCCTCTGTCTTCACTCAGCACTCTGAGGGATGGAAATTGGAGAGATGGTTGCTACTAA
Amino sequence
MMAEQVKCASAGVSSGAGSGPVVNAELEVKKLQELVRKLEKQNEQLRSRAASAAAAPHLLLLPPPPPAAPPPAGLQPLGPRSPPAATATAAASGGLGPAFPGTFCLPSPAPSLLCSLAQPPEAPFVYFKPAAGFFGAGGGGPEPGGAGTPPGAAAAPPSPPPTLLDEVELLDLESVAAWRDEDDYTWLYIGSSKTFTSSEKSLTPLQWCRHVLDNPTPEMEAARRSLCFRLEQGYTSRGSPLSPQSSIDSELSTSELEDDSISMGYKLQDLTDVQIMARLQEESLRQDYASTSASVSRHSSSVSLSSGKKGTCSDQEYDQYSLEDEEEFDHLPPPQPRLPRCSPFQRGIPHSQTFSSIRECRRSPSSQYFPSNNYQQQQYYSPQAQTPDQQPNRTNGDKLRRSMPNLARMPSTTAISSNISSPVTVRNSQSFDSSLHGAGNGISRIQSCIPSPGQLQHRVHSVGHFPVSIRQPLKATAYVSPTVQGSSNMPLSNGLQLYSNTGIPTPNKAAASGIMGRSALPRPSLAINGSNLPRSKIAQPVRSFLQPPKPLSSLSTLRDGNWRDGCY*