Special

RnoINT0131711 @ rn6

Intron Retention

Gene
Description
sodium voltage-gated channel alpha subunit 8 [Source:RGD Symbol;Acc:3638]
Coordinates
chr7:142610370-142611744:+
Coord C1 exon
chr7:142610370-142610511
Coord A exon
chr7:142610512-142611537
Coord C2 exon
chr7:142611538-142611744
Length
1026 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGT
5' ss Score
10.65
3' ss Seq
ACTTGGCCTTCATCTTTCAGACC
3' ss Score
10.55
Exon sequences
Seq C1 exon
GCAATGCCCAGAGGGATTCCAGTGCATGAAAGCAGGAAGGAACCCCAACTACGGTTACACCAGCTTTGACACCTTCAGCTGGGCCTTCTTGGCATTATTCCGCCTTATGACCCAGGACTATTGGGAGAACTTATACCAGCTG
Seq A exon
GTAAGTACGGCCTCTCTTTCTTTAGTGATATTGTCCTCACGGGGTTATGAGGAGCTGGGGACTGTCTGTGTGACACACCCACAGTGAAGACGTTAGGTGGGAGCCCTTGGGATGATGAATTCAGACAGCTCTTAGCCTGGTTTCTTGGCTGTTTAATCATGGTCAGCTGTGGAAGCTCACATCCTGACCCCCTCAGAGCACCCGCTTCCTCTCAGGTCAGGTTGCTCTCCGCACCCTGACTGCATCGTCTTCTGGATCTTCTGGTATCAGGACATTTGTTTAAGCAGCAGCAAACACTCATTTGTGCAGGGCATCTTCCTGGGTATTAAAACGAGGGGGAACTCTATCCCTGGGACCCTGAAGTGTGACTTAATATTTTTAGAGCTATACTGCATCTGGGCTTGTTCAGGTATGCAGTCCCCGTCCTATAATGACTTCACTGTCCTGTAATCCACAAGTCATAATGAGGAAAATCGGTGTCGATTGCTAATCTTAGAAATCCAGACGAGCCATTGTTTTTTTCTCTGGCTGGTGATGCTAGTTAGAAGATTAAAAAAAAAATAAATCTCCCCTTGCAAAAAGGAGCCTCTTCAAGAGAAGCTTCTGTTTCCAATCCCCAAGTCAGCCCTTACAGTTGAGCATAACAGACAGTAAATTCCACTAAGTGCTGGCTGATTGAAAGCATCAGGATGAGCTAGGCCTGTGCTGCGGGTCTGTGATCCTGGCACTCAGGAGCCGGGGGCAGGAGGATCACTGGGAGTTTAAAACCAGTTTGATTCACACAGCAAGTCCCATACCAGCCAGGGCTACACTGTAAGACCTTTTCTAAGATAGACAGACAGAAACAGAATATCTTTCTATGAAAGCAAAATCCAGGAGGCATTTCCCTCTCACAACGGAAGCAAGAGTTAAGCATTAGGAAGAGATTTGACCACTGGGATACGGGGTGGGTGCAAGGCACCACGCAAAGGAAACTCTGACCTCCTCAGCTGGCGACACGCTGAGAACTTGGCCTTCATCTTTCAG
Seq C2 exon
ACCTTACGAGCCGCTGGGAAAACGTACATGATCTTCTTTGTCTTGGTCATCTTCGTGGGTTCTTTCTATCTGGTGAACTTGATCTTGGCTGTGGTGGCCATGGCTTATGAGGAACAGAACCAGGCAACACTGGAGGAGGCAGAGCAAAAAGAGGCCGAGTTCAAGGCAATGCTGGAGCAACTCAAGAAGCAGCAGGAGGAGGCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000005309:ENSRNOT00000008160:8
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=0.072
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=FE(18.7=100),PF057587=Ycf1=FE(16.8=100)
A:
NA
C2:
PF0052026=Ion_trans=PD(12.4=44.9),PF057587=Ycf1=FE(24.4=100),PF0043013=ATP-synt_B=PU(72.1=89.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCAGAGGGATTCCAGTGCATG
R:
CTGTGCCTCCTCCTGCTGC
Band lengths:
342-1368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]