Special

GgaINT1011522 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr18:10088599-10089197:+
Coord C1 exon
chr18:10088599-10088832
Coord A exon
chr18:10088833-10089032
Coord C2 exon
chr18:10089033-10089197
Length
200 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
CCATCCTCCCCGCTGTGTAGGTG
3' ss Score
7.96
Exon sequences
Seq C1 exon
CCCGAGGTCAAGGTCTCCATCAGCCATTTCATGTCCTATGTGCATATGAGCGTGAAGGAGATGTCCCAGACCTACCTGGCTGTGGAGCGACGCTATAACTACACCACACCAAAGACCTTCCTGGAGCAGATAAAGCTCTACCAAACCCTGCTCTCTAAGAAGAGGAGTGAGCTTACTGCCAAGATTGAGAGGCTGGAGAATGGCCTGACAAAGCTGCAGAGCACGGCCTTGCAG
Seq A exon
GTGGGCATGGTCCGGCTCCATCCTGAGGAGGGATGGTGGGCACGAGAGCAGGGCTTCGCCCCACACAGAGCTCTCGGTTTGGGCAATGGGCCACGTGGGCTGCTGGGGCACGGGTGGCAATGCAGCCCCCAGCCGAGGAGCCCGCTGGTCCCTTCAGGGTTTGATGGTGCCCGACCTCTCCCATCCTCCCCGCTGTGTAG
Seq C2 exon
GTGGATGAGCTGAAAGCCACGCTGGCAGTCCAGGAGGCAGAGCTGAAGCAGAAGAACGAGGATGCAGATAAACTGATCCACGTGGTGGGCGTCGAAACAGAGAAGGTCAGCAAGGAGAAAGCCATCGCTGACGAGGAGGAGCTGAAGGTCCAGGCCATCAACACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007106:ENSGALT00000011513:56
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:
PF127802=AAA_8=PD(18.7=64.1),PF127772=MT=PU(4.4=19.2)
A:
NA
C2:
PF127772=MT=FE(15.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCACACCAAAGACCTTCCTGG
R:
GTTGATGGCCTGGACCTTCAG
Band lengths:
293-493
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]