Special

GgaINT0143168 @ galGal4

Intron Retention

Gene
Description
sodium channel, voltage gated, type IV alpha subunit [Source:HGNC Symbol;Acc:HGNC:10591]
Coordinates
chr27:1633711-1635282:-
Coord C1 exon
chr27:1635004-1635282
Coord A exon
chr27:1633765-1635003
Coord C2 exon
chr27:1633711-1633764
Length
1239 bp
Sequences
Splice sites
5' ss Seq
GTGGTACGT
5' ss Score
8.61
3' ss Seq
TTCTCTCCCAATCCCCACAGGCG
3' ss Score
10.82
Exon sequences
Seq C1 exon
GTGGTGGTAAATGCCTTGTTGGGTGCCATCCCCTCCATCATGAACGTCCTGCTGGTCTGCCTCATCTTCTGGCTGATATTCAGCATCATGGGGGTGAACCTCTTCGCAGGGAAGTACTACCGATGCGTCAACACCACCACGGGGGACCTCTTTGACATCAGCGTGGTGAACAATAAGAGCGACTGCATGGCTCTCCTCCACACCAACGAGGTCAGATGGGTCAACGTCAAAGTCAACTTCGACAACGTGGGCTTGGGATACCTGTCCTTGCTGCAGGTG
Seq A exon
GTACGTACCGATCACTGCGCATCGTCATAGCAGAGGGTCATCCATCATCATCGTCATAGCAGAGTCAGCAATTGCCATCGTCATAGCATGGGGTGAACAGCATCAAGGCTAAAGTGAAATGCATGTCTGAAGCCCACGCCAGGGTTCCTGGCTGCTGCTTAGCTCCAAGATTTAATTTAACCCAAAAACTGCAGGCTCGAGGAGGAAACAGGCAGGATAGAAGATGGGAGGGGAAAATTAAGTGTAGCAAGGGAACTGTTGGGGATGAGTACACAAAGCAGCAAGGTTGGAGCTGTGGGAAATCCTCCACAGCACGGCATGCAGGAGCAGGGAGGAGAAAGAGTTTTAAGCACCATTATTTGGAAAAGGAAGATGCTGTGACCCAGGGTCATAGAGCCACTTGAGCCTCTCACTTGCTCGACCTGTCTCTCAGTCTTCCCAAAATCGAGACTCCCATCCCCCCTTCGCAGCCTCCCTGCATGAAGATGTTCTTGCTAGAGTGAGGTCTGCGACAGTCATAGGCTGCAAGAGTTTTGGCTGGGGAAGATGACGACTGGAAAAAAGAGCATGTGAGCATTGGCCATGGGTGAATGCAGCCATGCTTCCATTGAACTCACCACAGCTGAGCAAGGCGAGCAGAAGGGGAACTGCTCACCACGACGTTAATAAAAGTACAGGTGTGGGCTCTGTTATTGGGTCACTCCCACTGGATCCAGGGGAACTAGTGGTTGCAGAACTAAAGCAGAACTCAAACTGATCAACCAGCTATAAACTCAGCTTCCTCTTCAAGGCTTGTTGTTTCCTCAGACTCAGGAAATAAGATGTTCTGGCTTTTTGCTTAACAAATCAACTGCAGAAGCCTATAAAAGATGCAAGACGCCCCCACCTCAGTGGGACAGAATCATAGAACCATAGAATGACTGGGTTGGGAGGGAGAATGGTTGGGCTTGGAAGGACCTCAAAGATCATCCAGTTCCAACCCCCCTGCCTTGAGCCAGGTTGCCAACCACCAGATCAGGTTGCCCAGGGCCGTATCCAACCTGGCCTTGAACACCTCCAGGGACATTCACAGACTCTCTGGGCAGCCTGTGCCAGCACCTCAACACCCTCTCCATGAAAAATTTTCCCCTGCCATCTGAACCCCAACCTAAACCCCAGAAGTGTCCCCATTGCCTTCCACTCCCTTCATAGCCCCATACACCTCCTGTTGAGCTTGCTCTTCTCTCCCAATCCCCACAG
Seq C2 exon
GCGACCTTCAAAGGTTGGATGGACATCATGTACGCTGCTGTGGACTCACGTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000252:ENSGALT00000040680:24
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:
PF0052026=Ion_trans=FE(40.4=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(7.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGGTGGTAAATGCCTTGTTGG
R:
GAGTCCACAGCAGCGTACATG
Band lengths:
326-1565
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]