Special

BtaINT0077913 @ bosTau6

Intron Retention

Gene
Description
integrin, alpha 6 [Source:HGNC Symbol;Acc:HGNC:6142]
Coordinates
chr2:24166158-24167069:-
Coord C1 exon
chr2:24166981-24167069
Coord A exon
chr2:24166277-24166980
Coord C2 exon
chr2:24166158-24166276
Length
704 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACC
5' ss Score
8.66
3' ss Seq
TGATGCCCTATTCATTTCAGGTT
3' ss Score
8.95
Exon sequences
Seq C1 exon
ATATTGCGGTTGGAGCACCCTATGATGGTAAGGGGAAGGTTTTTATCTATCATGGATCTGCGAATGGAATAAATACCAAACCAACACAG
Seq A exon
GTAACCAGATAACTTGGATTTCTATAGTTAAGGTCTCAGTAGTTTTCTTTCCAATGGATTGTTTAGATTTACGTGAATTTTCACACTAATCATGTGTTACTTACAAATCTAAAATTGTGTGAACTTTGGTTTTATAAAAATATGTATTAGAAAATAGCTTGTAAATAGATTTAAATGCAATGAGCTGCTTGTTTTAAACTGTAAAATTTCTTTGGTAAATTAAAAATCCAACTAAGCCAAAGGAAAAGACTGTTCTACCCTGGCAGCATAAGGAGATGGAATGTGATATATTTCCTTTAGTAGCATATTAAGAAGGGATGAAACTGGACAAACATAAGAGATGATTGTAATTGCATAGAGAATCAGATACCAAAATCTAAAAATTGCTTTAGAGGAAAATAAGACATTTGGAGGGCAGGAAGAGAAGTTTGGTTTGAAATACACTGATTGACTTAATATGGTACATAAGGTTATCAAAAATTCTCTTTGTCTTTTCAGATACAACATAAATCAGGTAACTTCTGTGAAAATAAAATGCATGAAATGTTTGATCATGTGTATGCTTATTTATAATTCAGTTGTGATTTAATATAATTTGTAAGTAAACTCTTTAACTTCAGTTCAAAAGAGACTTATCTTCAAAGCATAAATAAAAGGCTTATTTTAGTAGCCAGGTGTCCGTTCTGATGCCCTATTCATTTCAG
Seq C2 exon
GTTCTTGAGGGTAAGTCACCCTTTTTTGGATATTCAATTGCTGGAAACATGGACCTTGATAGAAATTCCTACCCTGATGTTGCTGTTGGTTCTCTCTCAGATTCGGTGACTATTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000017266:ENSBTAT00000022960:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.033 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF135171=VCBS=PD(4.1=10.0)
A:
NA
C2:
NO


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:
TATTGCGGTTGGAGCACCCTA
R:
TGAAAATAGTCACCGAATCTGAGAGA
Band lengths:
206-910
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]