Special

BtaINT0040863 @ bosTau6

Intron Retention

Gene
Description
collagen, type XII, alpha 1 [Source:HGNC Symbol;Acc:HGNC:2188]
Coordinates
chr9:14971598-14974203:-
Coord C1 exon
chr9:14974144-14974203
Coord A exon
chr9:14971862-14974143
Coord C2 exon
chr9:14971598-14971861
Length
2282 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGC
5' ss Score
7.31
3' ss Seq
ACGTATCACATATATTTCAGAAT
3' ss Score
7.52
Exon sequences
Seq C1 exon
TTCAAACAGGTGGCCCGACAAAGCCAGGGGAGAAGAAACCTGGAAAAACAGAGATACAAA
Seq A exon
GTAAGCATTTTCCTTAATATTTTATGTGGTTTTGCAGAAGTAAGTTATAAATGTAATATATAAAGGAGATGTTCCAATTCGATCCATAGTTTGATCTCACTCCTATATTAATTTCTGTAAGTTTTATCTACAAGTATAGGCAGTGTAATAGTAATGTACGGCTAAGTGGTTATAACACCCACATTCTTACTTTCTAACCATTCTAGGGACTAAATATTCTTTTTACTGGGGGTGTATTAAATGTGTGTATGTTCAAGTTTCCCTGCAGTATTCTGGCAGTAGGTGAAAAACAAAGCTCATCACTGGACTTAAATTGTAGAAACAGATGGTAGCTTAGGGACACATGGGAAATAGAAGGTTGGACCACAAGGGAGATGCCCTCGTGGTGTCTTTAGCAATTCCATTGCCGTGAAAATTGCTGTATATATTCTGGTCATCTCTAGGGTGTTTATGTGGGCTTACTTGGTGTGACTCTAAACATTTCCAGAGTCTCTGTAGGATGTCTCTGATGAATTGATGCATTTGTAATCAAATGAAAGCAATTTTATGGTCTGGTTTTGTGGTTTCTAGGCCCTTTTTATCCTACACTGCTCTGACTTACTGGGATAAAGCCTTAAGTGGTTGGACTTCTGATTTTGCCACCTTATAAATGGGATTTATGACTCGGGATAACAATAAAAATATTGTGAACACAAAGTTCCCTTTATCTGGAATTTTCCCCTCCAGATCACTGTTTATAATTCTTTATAATGTCTAATAATCTGAAGTGAAGTTTATAGCATGCAGTTACAATGCAAATATTTTCCCTGAATCATCAATATTTATTCTAAAGCAAAGTATTATTCCAAACATTGACTTTCAATAGACTTACGTTGGCCCATTAAATAGTATGCAAAAATTATTTAGGCAGGCAACTTGTATTGGCTTGCAAATTTTTCCAGGACCCTTTCCTTCTTTTCTGAGCCAAATACTTCTCTTATTATCCACCAACTGACTGCAGGGACAAAAATATCTTCAGAAAATTTACTCAGCTTTGCCTTATGAATACAGATTTTCGTAAAAACCAACCTGTTTCCCACTCACCAACTGACCACAGAGAGAAGAAAAAATATGTTTGATTACAAACACCAATTGTTGCATTTTTGGGGATTTAAAGATACCACATGTGTTTTTACTTTTGAGTTAAAATATTTTCCCTGCCTTTTCTTTAGTGAAAGTAGATTTAGTTGTGAAATTTAAATGCATTGATGATTTGCATTGAATGTGCAAATGCATTGAAAATATTATGGGTATTTTGCATTATATTTATGATATATTTATGATATTTATGGTACTTCTGTTAAGATTTCATTAACCCTCTGGGCTAACCAGCTGCCAACTTTAGACCATTACATTGTAAAGTGCAGGAGAATGTTAAAAGATTTGCTTTTTTCTTCAGCTCTATTGCATTTGCTTAAATGGCACAGCAATTGTTCTGTAATTTTACAAAAATATTTATTTGACTGCACCAGATCTTAGTTGCCTCATATGGGATCTAGTCCCCTTATCAGAGATGGAACCTAGGCCCCCTGCATCGGTAACGCAGGGTCTTAACCACTGGACCACTTGGGAAGTTCCTGTTTTGTATTTATTGATCTGAAAGTACCAAGAATGAAAACACTTCGCTTATATTTCTTTTGTATGTCTCCTAGATATTTTATATAATTTTTACTTGGAGAAAAGAGTGAGGATATAGTTATAAAAATAGATAAGTCAATAGCACAAATGCTTGGGTCATAGGCTCTTGGAGAATCGGTCATATATCTTTTCATCTTGTCTTGCACAATGTCTTCTATGACATTTTAAAGACATAGTTGCAGAAATGCATGTTCATGAAGGTACTGAAAATACTTCTGTGTGTGTGTTAAGTTGCTTCAGTCATGTCTGACTCTCTGTGACCCAATGGACTGTAGCCCGCCAGACCAGGCAAGAATACTGAAGTGGGTTGCCATGCCCTCCTCCAGGGGATCTTCCCAACCCAGGGATTGAACCCATGTCTCTTATGTCTCCTGCCTTAGCAGGCGGGTTCTTTACAGTGCCATCTGGGAACCTGCCTGAAAATGTGTGCCAATAAAATTTTGTGTTCTTTTGTGCATGTCAGTTGTGGGGGAAGAACAATATGAAATGTTCTAATAAACGAAATGATTTTAGGAGCCAACATTTTTGCAATGTTAGTTTGTATTCTTTAATGCTAGATAGATTTAATAGCATGTCATTTAAAAAACGTATCACATATATTTCAG
Seq C2 exon
AATGTTCTGTCAGTGCCTGGACTGATTTAGTTTTTCTTGTGGATGGCTCATGGAGTGTGGGAAGAAACAATTTCAAGTACATCTTAGACTTCATTGCTGCTCTCGTGTCTGCTTTTGACATTGGGGAAGAGAAGACAAGGGTTGGAGTTGTTCAGTACAGCTCTGACACCAGGACGGAATTTAACTTAAATCAGTACTACCAACAGGAAGAGCTGCTTGCTGCAATTAAAAAAATCCCATACAAAGGTGGCAACACAATGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000020056:ENSBTAT00000026725:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.714 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0009223=VWA=PU(46.2=89.9)


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:
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]