Special

BtaINT0129531 @ bosTau6

Intron Retention

Gene
Description
sodium channel, voltage gated, type VIII alpha subunit [Source:HGNC Symbol;Acc:HGNC:10596]
Coordinates
chr5:28221235-28223345:-
Coord C1 exon
chr5:28223061-28223345
Coord A exon
chr5:28221289-28223060
Coord C2 exon
chr5:28221235-28221288
Length
1772 bp
Sequences
Splice sites
5' ss Seq
GTGGTAAGA
5' ss Score
8.24
3' ss Seq
TGACTGACTCTGTTTGCCAGGCA
3' ss Score
6.51
Exon sequences
Seq C1 exon
GTGGTGGTGAATGCCTTGGTGGGCGCCATCCCCTCCATCATGAATGTGCTGCTGGTGTGTCTCATCTTCTGGCTGATTTTCAGCATCATGGGAGTTAACCTGTTTGCGGGAAAGTACCACTATTGCTTTAATGAGTCTTCTGAGATCCGATTTGAAATTGAAGATGTCAACAATAAAACAGAGTGCGAAAAGCTCATGGAGGGGAACAACACAGAAATCAGATGGAAGAACGTGAAGATCAACTTTGACAATGTTGGGGCAGGATATCTGGCGCTTCTTCAAGTG
Seq A exon
GTAAGATTGTTTTCAGTCCTGTGAGAATTGGACAGCTAGCAGAAATCTCCTTTCGTTCTTTTTCAACCCTATGTCCAGAATCAGGGTTGCTCTTAAGTAAGGGGTCACTGTCATTTCCCAAAGCAGATCCAGGGAGACACCTCTCCTGAGTACTGTGAGGTCTCTGAGACCTCAGTCAAGGGAATCTGTCATTGTGCTCAGAAGTTGAGTTCTGCTTAGCAAATAAGGATTTCTGCAACACAGTAAGGTTGCAGAGAGATCACCTTCTTTCTCCAGGACAGAAGTATGTAGTTAAAGAGAAAATAGGTAAGTCACAGACCAAAAAGAAAAAAAGGGCAATTTTGATGGAGCAGAACAATCCCACATTAACTGCTATGCCAGAGTTAACTGAAGAATATGACAATATGGTGGTGCTATGATGCTGCCACTATGTCATCTCAACTGCAGAGAAGGGTCTCCATGTATCACAGCAAGAAATGAAGCATTTCATCATGTCTAGTTTTCTCTCTCTCTCTGGCCAATTTTCTGGAGTGTTTGACAGGATAGTATGATGCAATGAAAACTCCTGGGCTTTGAAATCAGATGTAGGTTTGAGCCACACTCTGACATTTATTGGATATGTAACCTTGGACAAATTACTCAACCTCCCTGAGTCTTTTTCTTCATCTCTTAAATTTGAATAGTAATACCTTGCATGGTAGTTAAGAGGATTCATGGTGATTTATTAACATTCCCTAACAATGCCTGGCACACAGCAGGCATGTGCTTCATTAATAGTGTTTGCTCTTCCGTTTCTTTGTTACTATTACAACTGTTTTTACATCATATAGTTTCTGGGAGGATTAAATGTGATAGTGCAGGTGAAGCACTCAACTCAGCCTTGAGTGTAGTACAGTCTTAACTATTAGCTAGAAGGAGGCGGAGTTAATGGGATGAGCAGGGGTTTATCCCATTCCACAGCTCTTTAGTTGTTCTGTCCCGGTTCAAAAAATTGGACCCACAGATTGAACCAGAATTGGAGCAGCTTCAAGAAACCAGTGCCCATTAGCTGGCCAAATGTTGTATTGAGTCCCCACCATATGCTAGGCACTGTGCTTGGGCATTACCAGGGCCATCAGATGAATAAAGAACTGCCCAGGCCCTGAGAAAACTTAGAATCTGGTTGAGTTACTTAAATGGTAAACACGGAGGCTGTTAAATTGGTTACCCGTATTAGTTTCCAAAATCAGGTTAGGCACAATGGGAGAATTGAGTAGGGGCTGCCTAGGATAAAGCCGGTATTGCCACTACAGTAGGGTAAATGTGTGTTACTGAAGAGGGAAAAGTTCTAATTGAGGTTTTTTCTTAGTGAAACTATGAATTTTTCAAACCCCCATTACTTGTTTCACACGGTTTTAAAAATGACTCCTTCATAAAAGAGGGGTAAGTTCTAAGTAACATCAGTAGATCCCTGCCATTCATAAATACGAGTTTGCCCTTGCTTTAGGCAACCTTCTTAGACTCATTCTGAAGACCTTTTGTAAAAGTGTTGGCTCAACTACCATTGTCAACATGTTCCTTTGCCAGACTTTGATGTTATACTCAGGGACTTAGACAAAGCTCCCATGGGATCTGTATTAACAAACAGAAAATTTCTGCGTCCACTTGAGGCTGCACCCAAACTCCCCAACTTGTGTTCTCACAGAACCTAAGCCTGCCTTTTCGACCCTACCTAGACTCCCACCCACCCACCCGCTAACAGGCACAGTCTAATGACTGACTCTGTTTGCCAG
Seq C2 exon
GCAACCTTCAAAGGCTGGATGGACATCATGTATGCAGCCGTAGATTCCCGAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000021339:ENSBTAT00000061543:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=FE(40.9=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(7.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GTGGTGGTGAATGCCTTGGTG
R:
CGGGAATCTACGGCTGCATAC
Band lengths:
335-2107
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]