Special

GgaINT0048552 @ galGal4

Intron Retention

Gene
Description
sodium channel, voltage gated, type III alpha subunit [Source:HGNC Symbol;Acc:HGNC:10590]
Coordinates
chr7:19418383-19419950:+
Coord C1 exon
chr7:19418383-19418446
Coord A exon
chr7:19418447-19419808
Coord C2 exon
chr7:19419809-19419950
Length
1362 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAGA
5' ss Score
9.21
3' ss Seq
CCTGTTTGATTTTTACATAGGCA
3' ss Score
7.49
Exon sequences
Seq C1 exon
CTCATTTCTACATTTTGGAAGGACAAAGAGATGCCCTACTTTGTGGTAATAGCTCTGATGCAGG
Seq A exon
GTAAGACCCTTTCAAAAATCATCTGTTTTATTCTGTAGAAAAATCAGTAACATAAAGCCTACTTGTAGCAGTTGCAACTTCCCATTTAGCAGTGATACAGAACAATGATTTCTTTCTTAGGTCAAAATGTTCATTAACAGCCACTGTTCCTGCTTTATTAGAAATTTATCATGATAAAATCTGAACCCTACAAAGTCTACTCTGGAGATTAACTGAAAAGAGTAGGATGAAAACTAAAGTTAGAACTGAGAAAGAGAATGCATAAAATATCAAGGAAGTACAATGGCTACCTCATATTCCAAGGCTGAAAATTTTTTGTCACTGGCAAAATGTTCCATACACACATGTCCAATTGTTAGGCTTAACTGATATCTAACTGGCTTCTGTGACTAAGCTGAAAAAAAATTCAGCTTTTGTGAAGGAGATCCCTTGCACTATAATTGGATTTATCTAATCAGATTGTTTAATCTGTCTGTACTCTTAACAACATTTTAGCAATTATTTTTGCCAGGAAATTAAACATTCCAAATAGGTTCTATGTTCAAAATATGACTGAGGAGAACTTAAACACTCAGGTTAATTCAAATAGCAAATGGTTGAAAAAGATATCTTTCATTTACTCTTATATTTGTTTGTTTCTCAGAACATATTTCCTAAATTAACTTAATTATAATTTTGAAATTCGTAGATTTCCTGTGCAAAAATAGCAAATGCAGTCCCAATCCATTATGCATGCGTAGGTCGCTCCGAAACTAATGCCTCCTATTTATTTCCATGGAAACTACAACAAAGATAAAGAACACAGTAACACTGTTTGATAGACAAAATTCTCAGCTACAAAGGTCTATTTTTCAACGCAGTCACTATCATTAGTTGAACATTTTTGCCAGCAGTAAATGTGAGCCTGCATGCTGTGCACTTAAAAATCTGTACCAGTGGAGGTGACCCACTGTTGCTGTCACCACTGCTGAAACACACCACCCACCATCTCACTGTGCTCACATCCACTGCTGGATCTACATAAATGTTCAGTAAATGTTGATGAATGTCAATGGGTGCCATTTTTTTCCACATGAAGAAATTCAGTGGCACTGCTTTGCTTCATATACATTTCCATCTCAGACTCCATTTTGTCATATTGCCCCCTGTTGCCATTTATCACACAGCGCAAAATGTAACAGAATATTGGTGGGAAGGCTCAACTTCTGCTGCTATACTATCAAAATCACCCTCTAATGCCGTGGGCCAACATAATAAAATAGGCATTATTTCTGGAGTTATATATATATATGTACATACTTCATATACTACTGAGGAAAAGAAAAGTTATGAATAAATACCTCCTGTTTGATTTTTACATAG
Seq C2 exon
GCAGTGTCCAGAGGGATATATATGTGTGAAAGCTGGTAGAAATCCCAACTATGGTTACACAAGTTTTGACACTTTCAGTTGGGCTTTTCTGTCACTCTTTCGGCTAATGACTCAGGACTTCTGGGAAAACCTGTATCAACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011040:ENSGALT00000017981:7
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(7.8=100)
A:
NA
C2:
PF0052026=Ion_trans=FE(17.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTCATTTCTACATTTTGGAAGGACA
R:
CAGTTGATACAGGTTTTCCCAGA
Band lengths:
206-1568
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]