Special

BtaINT0061207 @ bosTau6

Intron Retention

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr7:18016725-18017507:-
Coord C1 exon
chr7:18017382-18017507
Coord A exon
chr7:18016848-18017381
Coord C2 exon
chr7:18016725-18016847
Length
534 bp
Sequences
Splice sites
5' ss Seq
TAGGTGAGC
5' ss Score
7.96
3' ss Seq
GAGTGCTGTGTCCCGTCTAGATG
3' ss Score
6.57
Exon sequences
Seq C1 exon
ATGTGGATGAGTGCCGTGTGCTCCCTCACCTGTGCCCTCATGGTGAATGCATCAATAGCCTTGGCTCCTTCCGTTGCCACTGCCAGGCTGGGTACGCGCCTGACACCACTGCCACAGCCTGCCTAG
Seq A exon
GTGAGCCCCCCGCCCCTTTTCTCTGAGCCTCTCCTTACAGCACCTGGCACACACTTCCATGAGAAAACCAAGTCCAGAAAGCAAAGCAGCTTCGTTTCTTTCCTCCACCCAACTCTATTTGGGCCGCTTTTCTCCTGTTATTTGGTGCATCCTAAGATTTTCAATTACATTGTGTAGCAGGGGTTCATCTAAATCAGGGTCAGCAAACTCCTGCCCAAAGGCTGAATCCGGCCCTCTGCTTGTTTTGTTAATAAAGTTTTATTGTCACACGGCCATGCCTGTTTGTCTTCTCATACAGTGGCTGTTTTTCCTGCTACAAAGACAGAGTTGAGTAGTTGGAATTAAGACCACAAAGCCAAATATATTTACTCTCTGGCTTTTTGCAGAAAAAAATGCTGGTTCCTTGGTTAAGCCCACAGATTCTGGTTGTCTAGGGTCTGGGAAAGAGGCCTCAACTGGGCCTGGGTGGAGAACCCCACCCCTGAGCCCCCAGGAATGTCTGTCTGACCCTCCTGAGTGCTGTGTCCCGTCTAG
Seq C2 exon
ATGTGGATGAGTGCAGCCAGGCCCCCACGCCATGTCCCTTCCTCTGCAAAAACACTGAGGGCAGCTTCCTGTGTGCCTGCCCCCGTGGCTACCTGCTGGAGGAGAACGGCAGGATCTGCCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000000595:ENSBTAT00000035613:59
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:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.2),PF0764510=EGF_CA=PU(0.1=0.0)


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:
ATGTGGATGAGTGCCGTGTG
R:
AGATCCTGCCGTTCTCCTCC
Band lengths:
243-777
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]