Special

BtaINT0061105 @ bosTau6

Intron Retention

Gene
Description
fibrillin 2 [Source:HGNC Symbol;Acc:HGNC:3604]
Coordinates
chr7:26847454-26848094:+
Coord C1 exon
chr7:26847454-26847504
Coord A exon
chr7:26847505-26847968
Coord C2 exon
chr7:26847969-26848094
Length
464 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
CTTGCTTCATTTCCCTGCAGACG
3' ss Score
10.42
Exon sequences
Seq C1 exon
ATACAGCTTGCCCAAGAGGGTTTGCCAGGATAAAAGGTGTTACTTGTGAAG
Seq A exon
GTGAGTAGGTTCTTAAAAACATTGTGAATCTTTAGGAAAGTATTTAAAATTGACATTCTCTCCCATACTTTGGAGATATTTATCATTCTCAAAAACCTTGGAATTTCGGTAAAAATACTCTTACGCTGTCAACAAATGTTTTAGAATAATACTTTTAGGAAACAGCTTTGAGTTTCCCATTTCTCCTCTTTATGCTGTGGGGTAAATTTTCATCCCTCGCCTTTAAGGCATAGAGCAGCTGGCAAAGAGCTTATCTCGGCTGTGTTTTATGGACGAGCAAGGCTGTGGCAGTTTTCACAGCTGGTACCCAGGGGACCCAGTAGCTTCGTTGTGAAATATATCTGCTTAACTGAGGTAATAATCCATATTATTGCAAAATGAATATGCTATACAGGAAGTAAGATTACACCTGCTTTTTCTATCGGTGACATCTTTATTCCTCTGCTTGCTTCATTTCCCTGCAG
Seq C2 exon
ACGTTAATGAATGTGAGGTGTTTCCTGGCGTTTGCCCAAATGGACGGTGTGTCAACAGCAAAGGATCTTTTCATTGTGAGTGCCCTGAAGGCCTTACATTGGATGGAACTGGCCGTGTGTGTTTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000015307:ENSBTAT00000020360:56
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:
PF0068312=TB=PD(17.1=38.9),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.3)


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]