Special

RnoINT0084005 @ rn6

Intron Retention

Gene
Description
laminin subunit alpha 5 [Source:RGD Symbol;Acc:621023]
Coordinates
chr3:175573249-175573973:-
Coord C1 exon
chr3:175573868-175573973
Coord A exon
chr3:175573349-175573867
Coord C2 exon
chr3:175573249-175573348
Length
519 bp
Sequences
Splice sites
5' ss Seq
GTAGTAAGT
5' ss Score
8.01
3' ss Seq
CCTGTTCTTTTCCAACACAGGCT
3' ss Score
8.47
Exon sequences
Seq C1 exon
GGCAATGGGCAGTGTTTCTGCAAGGCTCATGTGTGTGGCAAGACCTGTGCAGCCTGCAAGGATGGCTTCTTTGGCCTGGATCATGCTGACTACTATGGCTGCCGTA
Seq A exon
GTAAGTGCTCATACACCGCCCCCACCATGATCTGTGTTGTGTTATGCACACTGGAAGTCTGGGGCCCAGGGAAGTACAAGTGGGTCAGGCAGGGAGGGGTCTCATTCTGACAACAGCAAGAGGAGCAGATGTACACACACACACACACACACACACACACACACACACACACACACACACCAGTCAGCCAGCCAGCCAGCCAGCTTGTGCTGAGAGTATCTCTGTTCTGACACATGACCCTTTGCTCCCCATCCTGTGTTCCTAGCAGACATCACTAATCCATCCCAGTTCCCTTGCTCCTGCCCCCAAGCAGACCTTAAGAGTTGATGTTAGTTTATTTACTGAGGGTAGTAGATGCGAGAGGCTATGCATACATGACAGTTATCCAGGTGGACGTGCTGTCCCCTCTCTGGGCTTGGTAGGGACCTGCCTATGGGGCCTAACCTGGAGAGTTATGAGAGGGACCCCTGAGGGTGGTAGGGACCAGGTAGCCTCTGATCCTGTTCTTTTCCAACACAG
Seq C2 exon
GCTGCAGGTGTGATGTTGGAGGTGCCCTGGGTCAGGGCTGTGAACCAAAGACGGGTGCCTGCAGGTGCCGCCCTAACACCCAGGGCCCTTCCTGCAGCGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000053691:ENSRNOT00000081226:20
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(66.0=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:
GCAATGGGCAGTGTTTCTG
R:
AGGAAGGGCCCTGGGTGTTA
Band lengths:
198-717
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]