Special

BtaINT0084217 @ bosTau6

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr13:55422250-55422675:+
Coord C1 exon
chr13:55422250-55422430
Coord A exon
chr13:55422431-55422525
Coord C2 exon
chr13:55422526-55422675
Length
95 bp
Sequences
Splice sites
5' ss Seq
GGCGTGAGT
5' ss Score
7
3' ss Seq
TCCTGCCCCTCCCACCCAAGGCT
3' ss Score
5.75
Exon sequences
Seq C1 exon
GAAGGACACTTTGGCTTCGAGGGCTGCGAGGGCTGCCGCCCATGCGCCTGTGGACCAGCCGCCGAGAGTTCCGAGTGCCACCCCCAAAGTGGGCAGTGCCACTGCCGGCCAGGGACTGGGGGACCCCAGTGTCGCGAGTGTGCCCCCGGCCACTGGGGGCTCCCCGAGCAGGGCTGCAGGC
Seq A exon
GTGAGTGCGAGCAGGCGGGGTACCTTGGGGTGGCGAGTACCCCCAGGGTCCTCAGCCAGCTACTCACCCCGCCTCTCCTGCCCCTCCCACCCAAG
Seq C2 exon
GCTGCCAGTGCCAGGGGGGACACTGTGACCTGCACACGGGCCGCTGCACGTGCCCTCCTGGGCTCGGTGGGGAACGCTGTGAGACCTGCAGCCACCAGCACCAGGTGCCTGTGCCAGGAGGACCTGGGGGCCACGGCGTGCACTGTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000003061:ENSBTAT00000003981:47
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=0.039
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PD(24.4=18.0),PF0005319=Laminin_EGF=PU(95.8=75.4)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(2.1=2.0)


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:
CATGCGCCTGTGGACCAG
R:
GTGCAGGTCACAGTGTCCC
Band lengths:
176-271
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development