Special

GgaINT0129597 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr18:10081924-10082549:+
Coord C1 exon
chr18:10081924-10082081
Coord A exon
chr18:10082082-10082410
Coord C2 exon
chr18:10082411-10082549
Length
329 bp
Sequences
Splice sites
5' ss Seq
CAGGTACGG
5' ss Score
10.88
3' ss Seq
AACCTTCTCTGCTTCCCCAGACC
3' ss Score
9.17
Exon sequences
Seq C1 exon
GTGAAATGTGTTCAGGATGCAATTCGTGCTAAAAAGAAAACGTTCAATTTTCTCGGAGAGACGATATCGCTGGTGCCATCGGTCGGGCTGTTCATCACGATGAACCCTGGCTATGCAGGACGGACAGAACTGCCCGAAAACTTAAAGGCTCTGTTCAG
Seq A exon
GTACGGGCAGGCAGATGGGTCACCATTAACGTGGCACAGCTGTGACATGAACTGAAGCCATTGCTCATGTACACGAGGACACCCGTGCGTGCTGGTGGCTCTGCTGTAAGAGACCCCCGGAGCACTCAGCTCAGAGCTGTGGGGCTGCTCAGTACAGGAGGGTGCTCAGAGCACCTGGCTGTGTAATGCGGGCCGGCGGGGGGCTGCATGAGGTTGCCACCTGTTTCTCATTCTAACAGCAGCAGTGCATGATCTGAATGAAAAAACGGTGCAAATCTTGATGGCTTGTGGCTGTGTATGCACCCTGCTAACCTTCTCTGCTTCCCCAG
Seq C2 exon
ACCCTGTGCCATGGTGGTTCCGGACTTTGAGCTCATCTGTGAGATCATGCTCGTTGCAGAAGGCTTTATTGATGCCAAGCTCCTAGCAAGGAAGTTCATTACTTTGTACACACTCTGCAAGGAGCTGCTGTCCAAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007106:ENSGALT00000011513:37
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:
PF127742=AAA_6=FE(22.5=100)
A:
NA
C2:
PF127742=AAA_6=FE(19.9=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:
TGTGTTCAGGATGCAATTCGTG
R:
CTTGGACAGCAGCTCCTTGC
Band lengths:
288-617
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]