Special

GgaINT0087357 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]
Coordinates
chr3:28762983-28763528:-
Coord C1 exon
chr3:28763276-28763528
Coord A exon
chr3:28763174-28763275
Coord C2 exon
chr3:28762983-28763173
Length
102 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGA
5' ss Score
9.79
3' ss Seq
CTTTTGTTTTCATGATTCAGATC
3' ss Score
8.48
Exon sequences
Seq C1 exon
GCTCACTGGTAGATGATGAATCCCTGATTGGAGTTCTGCAAACAACTAAACAAACAGCTGCCGAAGTAACTAAAAAGTTGTCCGTAGCAGCAGAAACTGAAGTGAAGATTAACTCTGCTCAGGAGGATTATCGACCTGCTGCTACGCGTGGGAGCATTCTTTACTTTCTTATTACAGAAATGAGCATGGTCAATAATATGTATCAGACTTCACTGGCTCAGTTCTTAAAGTTATTTGATCAATCCATGGCCAG
Seq A exon
GTAGGAAAACACAGATCTTTCTACCATTCCAGTGTGTGTGTCTTTCCCATGTGTTTGTTGTTATTAAAATGCTTTTCTTGTCCTTTTGTTTTCATGATTCAG
Seq C2 exon
ATCTGAGAAGTCTCCCGTATCCCATAAAAGAATCTCAAATATTATTGAGTACCTTACCTATGAAATTTACACATATTCTGTTAGAGGCTTATATGAAAACCACAAGTTCCTTTTTACCCTTCTCCTGACGTTGAAAATCGATCTTGAGAGAGAACATGTGAAAAACACAGAGTTCCAGACATTCATTAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000010116:ENSGALT00000038200:56
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.012 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF127812=AAA_9=PD(10.0=27.1)
A:
NA
C2:
NO


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:
CGCGTGGGAGCATTCTTTACT
R:
TTTCAACGTCAGGAGAAGGGT
Band lengths:
245-347
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]