Special

RnoINT0083983 @ rn6

Intron Retention

Gene
Description
laminin subunit alpha 4 [Source:RGD Symbol;Acc:1560062]
Coordinates
chr20:44190172-44191713:+
Coord C1 exon
chr20:44190172-44190327
Coord A exon
chr20:44190328-44191553
Coord C2 exon
chr20:44191554-44191713
Length
1226 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGC
5' ss Score
9.88
3' ss Seq
TCTTCTTCTTCTTCTTTCAGATT
3' ss Score
12.93
Exon sequences
Seq C1 exon
GTGATATTTATTCGGGAAAAGAGCAGTGGCCGATTGGTCATTGATGGTCTGCGAGTCCTCGAAGAAAGGCTCCCCCCTAGTGACGCTGCCTGGAAAATCAAGGGTCCCATTTATCTGGGAGGAGTGGCTCCCGGAAGGGCTGTGAAAAATGTCCAG
Seq A exon
GTAAGCCGGCTGTGGCAAGGCTGAGCCACTGACCCCTTGAACCGGAAAAACACTGATTCCCGGTTCTCATTTTATAGAGTAGGAACTTAGTCAAAGTGGAGCAGTTTGACTTCAAAATATATATCCTGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCGCAAGGCCCTGGGTTCAGTCCCCAGCTCTGGAAAAAAAAGAAAAGAAAAAAAAATAATATATATATCCTAGACTGTCCTGTAGGATTCCTGCCTGCCCTGGGCATTTTGACTTTTAAAATAGAAATGAGATTTTAAAAAAAAGTTTAATAGGTATAAAATGCCCTGGAATTTACATCTCCAGAGGGGGTTTATTAGTTCTGCAAGTACCTATAATTTTAATAAAAAGCTACAGTAAGACCAGAGAACAACCCATTCTACCATATTACTGACTGGGAAAAATAAAAACCTTCATCTCCTTTCAATTCGGTTCCACTTTTTCTCTTTCTCACAATTTCTAAATACTCACAGAGTGCACATGTAAGTGGGAGAATTCAGAATCTAAGAAACATTTTTGTAAATCAAATTACAGCTAATACCTCTTTTTAAAAGGGTTTCTCGGTGAATGGAAAGGATCAAAGGTCTTAATTTATCTGAAACACAAACGTAGATTTGATTTTATCCCAGGGTCAGTACATTGCTAAGATCCATTGGCGGTTTTCACTATAATTAGACTTGAAGTAAGCAGCCAGTTCTGTGGCTGTCATTTTTACTGTTCCCAAATGCGGTCTAAAACCCATTGTGCGCAGTGACACAAATGTCATATCCCGTAGTGTGATAAATTCATAACTGCATTACGAGCTAATGAAGCCAGCTCGGCAAGCTTCTCCCTGGTGGCATAGAACTTCCATCCACATCCGTGATCTGGGACCCAGCTACCCTCCTGAAGGAAAATGAATGGTAGTACGCTCGTCAACTAGAAAACCACAGTTGCAACTCGTTTTGTCGCTACCTGTGGAAACATTTCCAATGCTCAATAACTACACGCTGATGTTGTGAAATACAAAATCCCAGCTTTGAGGAATTAGTTAAAAGTAAGTGCCAGGAAGAAGCCACGTCCCTCATTCAGAACGCTAAAATGAACAAGGGGTAACTCACTCGTTTGCTTTCCCGTGGTGCATCTGGGCGCTGGGCAAGGGTATTTTAAGCAATTTCTTCTTCTTCTTCTTCTTTCAG
Seq C2 exon
ATTAACTCAGTCTACAGTTTCAGTGGCTGCCTTGGCAATCTCCAGCTCAATGGAGCCTCCATCGCCTCTGCCTCCCAAACGTTTAGCGTGACCCCTTGCTTTGAAGGGCCAATGGAGACGGGGACTTATTTCTCCACAGAAGGAGGCTATGTGGTTCTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000000599:ENSRNOT00000000737:33
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:
PF0221019=Laminin_G_2=FE(39.8=100)
A:
NA
C2:
PF0221019=Laminin_G_2=PD(14.1=33.3)


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:
TTTATTCGGGAAAAGAGCAGTGG
R:
CTAGAACCACATAGCCTCCTTCTG
Band lengths:
310-1536
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]