Special

BtaINT0084189 @ bosTau6

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr13:55409127-55409741:+
Coord C1 exon
chr13:55409127-55409232
Coord A exon
chr13:55409233-55409641
Coord C2 exon
chr13:55409642-55409741
Length
409 bp
Sequences
Splice sites
5' ss Seq
GCAGTAAGG
5' ss Score
4.69
3' ss Seq
CACTCACTCCCCCATTGCAGGCT
3' ss Score
8.78
Exon sequences
Seq C1 exon
GGCAACGGCCAGTGCTTCTGCAAGCCCCACGTGTGTGGCCAGACCTGCGCGGCCTGCAAGGACGGCTTCTTCGGGCTGGACCAGGCTGACTACTTCGGCTGCCGCA
Seq A exon
GTAAGGCCCACTGCTTGGCCCTTGGACCACGTCCCGGAGAGGCTGAGGCCCAGGGAGGGACACATGGGACAAGGGCAGCCAGGGCCTGGGTGTCACATGGCACTCGCTGAGCCACTCTGGGTACCTGGCCAGACCTGTGCTGGTGTGGAGGGGGTGCGGATTTAACCCCTTCTTCTCCCTCCATCCCATGCCCTGGCAGGCGTCACTCACCAATCCCAGGGCCCTTGCCCTAAATCCTGACCCTCTGCTGTCCAGAGCCCCGGGCAGCTCCTGGTGGCAGTAACACTTGTCCTCTCAGCCTGGGTCACCCTTGATGGAGGGTGGACGAAGCAGAGTCCTGAGCTGCGGGCTGCGGGAGGAGCATGGAGACCGTGGGGCTGGGCCTCACTCACTCACTCCCCCATTGCAG
Seq C2 exon
GCTGCCGGTGTGATGTTGGCGGAGCGCTGGGGCAGAGCTGTGAGCTGAGGACGGGTGCCTGCATGTGCCGCCCCAACACCCAGGGCTCCACCTGCAGCGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000003061:ENSBTAT00000003981:20
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:
PF0005319=Laminin_EGF=PD(64.7=91.7)
A:
NA
C2:
PF0005319=Laminin_EGF=PU(72.7=94.1)


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:
GCAACGGCCAGTGCTTCT
R:
CAGGTGGAGCCCTGGGTG
Band lengths:
199-608
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development