Special

GgaINT0011780 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8200295-8200979:-
Coord C1 exon
chr20:8200871-8200979
Coord A exon
chr20:8200393-8200870
Coord C2 exon
chr20:8200295-8200392
Length
478 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGG
5' ss Score
8.3
3' ss Seq
CTCCTTTCCATGCACGGCAGCAC
3' ss Score
4.79
Exon sequences
Seq C1 exon
TTTCCTTTGTCGAGGGGTTGCTGTGGATTCCCAGAGCAGATTGGCAACTTTTGAACTTACCTCGGAGGCCACGATTCGGTTCATCGCTGACCTGGCTGACTTCTTCCTG
Seq A exon
GTGAGGCTCCCTATGAGGGTTGCTGTTTGCAGGTTATGAGGAGGAGAGGTGGGAGAAGTGCCTGGCCGGCAGAAGGGCTTTCTGGCTCTGGTTTGGCTGGATGCTAGATCTCCATCCAGGTCATGTGCAGTCCAAGGTGAAGAGCGTGCTAAGTAGCATGTTTTGAAATAGATAGTTGGGTTTGGGAGAAGATGCTGACAGGAAGCTGCTCTTTGTGGAAGGAGCTCTGCAGCAACGTGACAGCGCTTCTTCCCACTTTACCTGGAGGCATTCGTGGTTGCTTAGATGGAGATAGAAGTGGAGCTCCTAAACACATTAGGGCTTGTACCAGGGAAGAAGGGGCAGGAAATAGGCATGACCTGTTATGTGTTAGCCAGTGTCTGATGAGAGGATGTTTGGTGCACTGATGGTGGACTCAGAAGCCACTGTAGGCTCCCAGACTCACTGTAACTGTATGTCTCCTTTCCATGCACGGCAG
Seq C2 exon
CACAAAGTGTACCTTGTTCCTGCTGAGCAGTTCACCATGGAGTTTGTTGAGCCGAAGGTGCATTGCATCAGTGTCCATGGCATGTTCTCATCCAATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:24
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTTCCTTTGTCGAGGGGTTGC
R:
TATTGGATGAGAACATGCCATGGA
Band lengths:
206-684
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]