Special

GgaINT0035383 @ galGal4

Intron Retention

Gene
Description
laminin, gamma 1 (formerly LAMB2) [Source:HGNC Symbol;Acc:HGNC:6492]
Coordinates
chr8:7486252-7486833:+
Coord C1 exon
chr8:7486252-7486441
Coord A exon
chr8:7486442-7486720
Coord C2 exon
chr8:7486721-7486833
Length
279 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
AGCATGGCTCTTCTCCCTAGGCT
3' ss Score
7.98
Exon sequences
Seq C1 exon
GCAAATTCTTGGGCAACCAAGTTTTGAGCTACGGTCAGAACCTGACCTTCTCCTTCCGTGTGGACAGACGGGACACACGTCTCTCAGCAGAGGACCTGGTACTGGAAGGGGCCGGGCTGCGTGTGTCGGTGCCTCTCATTGCCCAGGGCAACTCGTACCCCAGTGAGAGCCCACTGACCTACACCTTCAG
Seq A exon
GTGAGGGGGTCCAGCCCAGCCCAATGGGAGCCCAGAGAGCAGGTGGGACCCAGTCTGCCACACACCCTGCCCTCTCAGCTCCTGGGAAAAGAAACAGCAGTAATTTTAGCTCATGAGAGTGGTCTTATCAGGTTAATTTGAAGCTGGCTGTTCAGCAGGTTGCTTAAGTGGATGCAGAGTATGTGGCAATTGCATACCTTGGTTGGAAATGGTGCTTTAAAAGGGCACAGCTGCTAGCATCTGAAAGCTTTGCAAATGGAGCATGGCTCTTCTCCCTAG
Seq C2 exon
GCTCCATGAGGCTGCTGATTACCCGTGGAGGCCTGCTCTCTCTGCATTTGACTTCCAGAAGCTTCTCCACAATTTGACTGCCATCAAGATCCGTGGAACATACAGCGAGAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004620:ENSGALT00000039414:10
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:
PF0005213=Laminin_B=FE(48.1=100)
A:
NA
C2:
PF0005213=Laminin_B=FE(29.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGCAACCAAGTTTTGAGCTACG
R:
TTCTCTCGCTGTATGTTCCACG
Band lengths:
292-571
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]