Special

RnoINT0084163 @ rn6

Intron Retention

Gene
Description
laminin subunit gamma 1 [Source:RGD Symbol;Acc:621052]
Coordinates
chr13:70682307-70683150:-
Coord C1 exon
chr13:70682905-70683150
Coord A exon
chr13:70682461-70682904
Coord C2 exon
chr13:70682307-70682460
Length
444 bp
Sequences
Splice sites
5' ss Seq
AAGGTTAGT
5' ss Score
8.54
3' ss Seq
TCTCTGTCTTCCCACCCTAGCCT
3' ss Score
8.61
Exon sequences
Seq C1 exon
GCAAGAGATGTGAGCTCTGTGATGACGGCTACTTTGGAGACCCTCTGGGCAGCAATGGACCCGTGAGACTCTGCCGCCCATGTCAGTGCAACGACAACATAGACCCCAACGCAGTTGGCAACTGCAACCGTCTGACTGGAGAATGCCTGAAGTGCATCTATAACACGGCTGGCTTCTACTGCGACCGGTGCAAAGAAGGGTTTTTCGGAAATCCCCTGGCTCCCAATCCAGCAGACAAGTGCAAAG
Seq A exon
GTTAGTCACTGGCCAGACTCAGTCCCGCGCACGCCTTGATGTGCAGATCCGCCGTGGGGTCTCTTTCAGTGCCTACAGAAGTTTGTGCAGTGTGAACCATTTGCAGAACTTAAAATGGCTGCACTCCGCACCAAAAAAAAAAGTGAAACAGGAGAATTTATTATGTTGACAATGTAGCGGATGTTTTATTGCTTGTTATTATTCAGGTAATAATCAGTTAACAACTCTGAATACGATGGTTCTCTTTTCACCCTGTGTTTACAAAGTCAGTGCATGTTTTAATTGACAGCACATCTCTGTTCAGATTACTAAGACAAGACTCTCTGTGCCTGGGCAGCTTCTGTACGAGACAACGCAGGCCTAAAGAACCTGTTCAAGTGTCTCATGCTTTAGTGCTCTCCCTGGTGATTCGCATCTGTGACTGTCTCTGTCTTCCCACCCTAG
Seq C2 exon
CCTGCGCCTGCAATCCCTATGGTACAGTACAGCAGCAGAGCAGCTGTAACCCAGTGACCGGGCAGTGCCAGTGTCTGCCTCATGTGTCAGGCCGGGACTGTGGCGCTTGTGACCCTGGCTTCTACAACCTGCAGAGCGGGCAAGGCTGCGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000002680:ENSRNOT00000003605:14
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(42.3=26.5),PF0005319=Laminin_EGF=WD(100=65.1)
A:
NA
C2:
PF0005319=Laminin_EGF=WD(100=94.2)


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:
CGGCTACTTTGGAGACCCTCT
R:
CTGCAGGTTGTAGAAGCCAGG
Band lengths:
355-799
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]