Special

GgaINT0008957 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr15:4875925-4876589:-
Coord C1 exon
chr15:4876422-4876589
Coord A exon
chr15:4876114-4876421
Coord C2 exon
chr15:4875925-4876113
Length
308 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGTG
5' ss Score
6.13
3' ss Seq
CTGATCACCTTTCTCTGCAGGAG
3' ss Score
10.18
Exon sequences
Seq C1 exon
GTACAAGGACATATCAAAAACCTGATTGAAGAGAATTTCAACGATGAGTTGGAACAGGCTATGAGGGATCCTATTCTTTTTGGAGATTTCAGGATGGCACTGAATGAAGGAGAGCCTCGTATTTATGAAGATATACAAGCCTATGATGTGGCAAAAAATCTCTTTCAG
Seq A exon
GTAGTGTGCTTCAACTTGGAACTGTGTGTGATTTTTGTGTCTTTGCGTGAGGAAGAGTAAGGAAATTGCATCAAACAAGGTGAAATCAGTTCTTCTATGCACACGTACAGCAGTGTGCACAGAAGACTCTCATTTGGCATCTGCAGTAATGGAAATTGAGGGTCAGCTATGGAGTTTGCAGTGCTTTCCAATTATTTATTTTCCTTGATGACCTTTTCAAGAAATAATGCAGCTAAATGGGTTGTTATTTTATTAATGCTATTGTTTCCTTGGTCTCCTAGCAACATTCTGATCACCTTTCTCTGCAG
Seq C2 exon
GAGATTTTGGAGGAATATAATGAGGTTAATCTTAAAATGAATCTAGTTCTTTTTGATGATGCTTTGGAACATTTAATCCATGTGTATCGCATCATACGGATGGATCGTGGCCATGCCCTACTCATAGGAGTTGGAGGCTCAGGAAAGCAGTCTCTTACGAGATTGGCTGCCTTTACAGCTGGATGTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000003170:ENSGALT00000005023:49
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:
NO
A:
NA
C2:
PF127802=AAA_8=PU(21.3=90.5)


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:
ACAAGGACATATCAAAAACCTGATTG
R:
TGTAAAGGCAGCCAATCTCGT
Band lengths:
343-651
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]