Special

GgaINT0129587 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr18:10079271-10079731:+
Coord C1 exon
chr18:10079271-10079397
Coord A exon
chr18:10079398-10079578
Coord C2 exon
chr18:10079579-10079731
Length
181 bp
Sequences
Splice sites
5' ss Seq
GAGGTATGG
5' ss Score
8.98
3' ss Seq
CCTGCTGCTGCTGCCCACAGGTG
3' ss Score
11
Exon sequences
Seq C1 exon
GCTGGCGGTCTGTGAGAAGGCTCTGGCCGAATACCTGGAGACAAAGCGACTGGCCTTCCCCAGGTTCTACTTCGTTTCCTCCGCGGATCTGCTTGACATTCTATCTAATGGGAACGAGCCAACTGAG
Seq A exon
GTATGGGCTGAGCACAAACCAGGAGGCGCAGCCCACCTCAATCACGTCCTGACATATTGCAGATGTCTTAAAATCTCCGAACTGAACAGTGTCCCTGACCCGCTGCGGCACAGGGATGCAGCACCCTGAGCTGCAAAACGCCCTCTGACCCCAATGGGGCTCCTGCTGCTGCTGCCCACAG
Seq C2 exon
GTGTCCCGTCACCTCTCGAAGCTGTTTGACAGTCTCGCTAAGCTGAAGTTCAAGATGAGCCCGGACAAAAAGCCGCTGAAGACGGCCCTGGGGATGTTCAGCAAAGAGGAGGAGTTTGTGCCGCTGAGCGCAGAGTGCGATCTGTCCGGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007106:ENSGALT00000011513:29
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:
PF083938=DHC_N2=FE(10.1=100)
A:
NA
C2:
PF083938=DHC_N2=FE(12.1=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:
CGGTCTGTGAGAAGGCTCTGG
R:
CGGCACAAACTCCTCCTCTTT
Band lengths:
245-426
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]