Special

BtaINT0077910 @ bosTau6

Intron Retention

Gene
Description
integrin, alpha 6 [Source:HGNC Symbol;Acc:HGNC:6142]
Coordinates
chr2:24168107-24171533:-
Coord C1 exon
chr2:24171402-24171533
Coord A exon
chr2:24168318-24171401
Coord C2 exon
chr2:24168107-24168317
Length
3084 bp
Sequences
Splice sites
5' ss Seq
TAGGTAGGA
5' ss Score
7
3' ss Seq
ACCATGTTTTGTTTTTCTAGGCT
3' ss Score
10.2
Exon sequences
Seq C1 exon
GGATTGTTCGTGTAGAGCAAAAGAATAACACTTTTTTTGACATGAACATCTTTGAAGATGGGCCTTATGAAGTTGGTGGAGAGACTGACCATGATGAAAGTCTAGTTCCTGTTCCTGCTAACAGTTATTTAG
Seq A exon
GTAGGAACGAGAGTAGATGACATGCCTACCTCCTCAGATGCCTCTGTGTGACACCGCTGTCACAGGACCCTGGACTGTGAGGCTGAGAAAAGGCCAGATTGGGGCTGGGGGCCTGTGGCTGCATTTAGTGGAATTTAAAGCTTGGTGATCCCTGAGGTATTCTGACTGATTCTTGTGGTATCTGACCTGAGCTGCCTCAAAGCAGGAGGAAACCTACCGTCTCCTAAAATCTTCTGTCCTGCGTGGAGGTCTGTTTCCCGAGCTAATGTCCGCTTCTGTAACCCGCACCAGGCGGTCCATGCAGCCATGACACCATGCGTGGTTGTAAGCAAGAGGCCGAGTTGTCTTCCCTCTCCGTTCAGAGTCTCTTTTTGGAGAGCTACTCTTGAAGAGCTACATTTATGAAGTTACTCGTAAGTGGCAGGTCAAGACCTCCAGGTCCATCCTTTGTGACTGCCCTTCTCCAGGGGTTGGCCTCGCTTCTGGATTGTCACAAGGCCCCTGGCCGGTGGCATGGGGGCTTTCCAGCCGAGCCAGAGCCGCACTGCTAAAGCAGCTCCGAGGACACCCAGATTGTGGTCTAAGTGCCAATTCCTTAACTCCTAACGCTTGTTTGCGTTACTAATGGGTGTCCTAAATTATTCATGTGCATTATGGTAATTACACAAAGGCTTTTAAAAGCTTTAATTCTTGGTATGAGTTGACATAAAGAATAATTACTGTGTAATTCTTGGAAAAAAATGTAAAAAATCTACTAAATCTAAATAGTATCCTGTTCTTTTTAAAAAATAGATAAGTACCATATGCTGGAGATCTTACTAGAACAATGGAAGGTTAAAAAGGGGAAAAAAATGGGTGTAGATCTAAAAATAATTCTAAATAAGGTATTAATAAACATATTCTTTAAAAATTGTTCTAATTATATAGATATGTATAAACATACTGTTAATTAAAAAAAACTTTTCAGAAACTCCCCCACCCCTAAATTAAGAATTTGATGTGAAGACATAGAATGGAGAAAACTTATACTTACCACTTGTTAAGCACCTACTGTATGCTATAAATCACACACTATTACTACTTTATAGGTCTTATTTGTTCTTTCCAACTATATTATAAAATAAATATTATTTTCCTTTTGCTGATGGGGGAAAAAATGCCTGTCACTGAGGGAAATGAATTTCCTAGTCCAAGGTCACACAATTAATACTCCCCCAGCCAAGGGAAGAAATGCTCATGAAAATGATTGGGACAGGGTGGGAAGCAGCTGGGTATGTGAATGCTTTCAGTGGCTTTGCAGGACAGGAGGGGAACACAGGGCTGAGTGGTTTGCAGTCTCAATTATTAAATAGGATTTTCCAGGGCAAAATTCTTTTCAAGGTAAATATTAATACTCTCAGTAAACCAATATTTTAATTGAATAAATTTTAACAGTCTCTTCAAATGAGTTACTTAATTTATGCCATTTCAATTTAATGTTTCTGGTCAAGAAGCCAACACTTTGGTTCATAAGATAGATGCCCGTGGATTTTATCTTAGTGTCTACTGGAACATGTGAAACTATTAAACTTTTTTTTATTAAACACATTTGCCACTTTCAGAATGGATTTCCTCAAAAGCGGGTACTGGGTCGGGGTGGGGAGAATAGTGTCACATTTCTACTGTTACATTTTGGCTGTCTGTGCATCTGTCATTTCGAAAAAATCAGCAGGTTTTAGGAGGAAAATGATCTGCATGAGGTTTGGAAGCTGGCAAAGAGGGTGGCTTGCCGGATGCAGCAGTGGCCTCAACATTGCGAGCACGGCAGTAGCCGGTGTGCCTCTTACCAAGCATAATTGCTTTTTCTTCAATCTCTTCCGTCCCGTGCATGTGTACAGGCCTGCTGTTTTTGACCAGCGTTTCCTATACAGATCCCGATCAGTTTGTTTATAAAACACAGCCTCCCAGGGAGCAGCCCGACACATCCCCTGATGTGATGATGAATAGCTACCTAGGTTTGTGACCTCTGAGATGACAAATAAATGGTCTTGGTCATGGTCATTTAAGAATTTTTTTTTTTTTGATCCATATAGAGCATAAATCTTTTTATTTTCTATTTCATTTCAAGTGAAGCACACACAAAAAGCATGCTGCAGTTGAGGCTCTGCAGCCAGAATGGCTTCCAGAGCTGGATTCAATTGTGTCTCCTTTATAAACTTGTATCCTGTTTTTCAACACGCTTCACAATTTGAGAACTGCAACAGTAGCGGTGATGCTTTTCATAAATAAAACCCAATTAAAAGGGTGAGCTTATAGTATTCTGCATCTGCCTCGTCTTCACATAGGAAGATTTGCTTTATTTGGACAATTTTGATGCGTGGACATTTGTGTCTGCTTGCCATTTAACCTCAGTTGGTAATCTGACATCCTACCTGATGCTTTATAATGAGGTTTCTAATGTTTTTCTGCCCTCTGAACAAGTGTGTAATTGATACAGATGACAACTTGCTCACCTCTATTGTTTACGCTAGGTTCTCAAATCTCATCAGTCATGGTTTTGTTTGCATGTTTGTGTCTGAGAACTAAGTTGGCCCTAAGGAGTAAAATGCTGGCTGTGGTATATTAATGTTGTTAGCATTCTTTTATTGCCTGATGACCAAAGAGATTGATGAATATACAAGTTACTAATCACTGCATTATAGCAAGACCCATAGGCACTCAGTTATGCTATGTCAGGTTACATCTTGGTGTACAGGATGTAACTTTCCCTGGATAATTTAGTATCTAGCTTGATCTCCTTTTACAGCAGTTTCAGTATTGGAATGGAGTTTGAACTGATTCTTAAGTAGCATGTATGCTTCATGATTGAAGTTACACAAATGCTAACTAGCACAGGTGCTTTTTTAAAATGCCTTAACAGGGAAATACCTACTATTTTATGCTTGAGTCAAATCTCCTGGTTCTGTAATTCTTATCATAGATATGATAGCTGGTGGGGAGGGTCAGAAGGAGAGTGGTGGGAAACCACAGGTAGTGATGAAGTAACCAGTGTTAGATACCTCCTGAAAAACAAGAGTTGATAAGTACCATGTTTTGTTTTTCTAG
Seq C2 exon
GCTTTTCTTTGGACTCGGGGAAAGGTATTGTTTCCAAAGATGAGATCACTTTCGTGTCTGGTGCTCCTAGAGCCAATCATAGTGGAGCGGTGGTTTTGCTTAAAAGAGACCTGAAGTCTGCGCACCTTCTCCCTGAGCACATATTTGATGGGGAAGGGCTGGCTTCTTCATTTGGCTATGACGTAGCAGTGGTGGACCTCAACAAAGACGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000017266:ENSBTAT00000022960:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.111 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF135171=VCBS=PU(6.8=7.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]