Special

RnoINT0132814 @ rn6

Intron Retention

Gene
Description
semaphorin 3B [Source:RGD Symbol;Acc:1310079]
Coordinates
chr8:116355942-116356607:-
Coord C1 exon
chr8:116356388-116356607
Coord A exon
chr8:116356034-116356387
Coord C2 exon
chr8:116355942-116356033
Length
354 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGG
5' ss Score
7.2
3' ss Seq
CTTTCCTTTCTTTTCTTCAGATG
3' ss Score
12.53
Exon sequences
Seq C1 exon
TGCCCCAGCAAGACCTTTGGCACCTTCAGCTCCACCAAGGACTTCCCAGATGATGTTATCCAGTTTGCTCGGAACCACCCCCTCATGTACAACTCAGTCCTGCCCATGGGGGGGCGCCCTCTCTTCCTACAAGTGGGAGCTGGGTACACCTTCACCCAGATCGCTGCAGACCGGGTAGCAGCAGCCGATGGACACTACGATGTGCTCTTCATCGGCACAG
Seq A exon
GTCAGGGTCCCACCACAGTGCCCACAGGACTGAGAGCCCCTCCAGGTTCCTTGGCCCAGAGTAGAAGTTGTTCTTGGTCAATCTAATATCTACATCTTTGTCTGAGCTGTGGCCCCGCTTTCTGAGGTCTCCCCTCATTGTTTCAACCCATAACTGTTACTTTTTCATGACCCAATCATGATGAAGGTAGAGGGCACAGGGCTAGAGCACATGTGCATGCACTCACACACACATGCATGCACACACACACACACACACACACACGCACACACACATGCACACACGCACACGCACATATACACACATGGCTCGTTAGGGAAACCCAATAGTCACTCTTTCCTTTCTTTTCTTCAG
Seq C2 exon
ATGTGGGCACGGTGCTGAAAGTCATCTCAGTCCCCAAGGGCAGCCGACCTAACTCGGAAGGACTTCTCCTGGAAGAGCTGCAGGTGTTTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000016512:ENSRNOT00000066296:12
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:
PF0140314=Sema=FE(16.5=100)
A:
NA
C2:
PF0140314=Sema=FE(6.8=100)


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:
GCCCCAGCAAGACCTTTGG
R:
TCAAACACCTGCAGCTCTTCC
Band lengths:
310-664
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]