Special

GgaINT0008949 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr15:4881297-4881952:-
Coord C1 exon
chr15:4881818-4881952
Coord A exon
chr15:4881514-4881817
Coord C2 exon
chr15:4881297-4881513
Length
304 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGG
5' ss Score
7.61
3' ss Seq
TTTGACTTTTTTTACGACAGGTG
3' ss Score
8.96
Exon sequences
Seq C1 exon
CAAGAGAGAATTGAATTGAATCGTTTATTCGAAAAATATGTGCCCTGCCTTATTGATATGATTACAGAGGGAATTGTGGATGGCAAACAAGAAGAAAGGCTGAAGACCATTGTTCCTCAAACAGATTTAAATATG
Seq A exon
GTGAGGAATAGAAAATAAAGGTTGAAAAAGTTTTTCTTAGAAGTGGAGCTGACTAACGAAGACAAAAGTCTCCCAAGGAAATCAGGGGTGTAGTGTTTACAGTGAAATGTCAGTTTGCTACCAAGAAACAACAGAAACAGTCAGTTCCTTACCAGTGCTGTCCTGCTGTCATTAATACTTGTATCAGTAGATACATCTGTAGCGACAAAATATCAGCAAACACTCAAACAGCTGAAAACATAGTAAGAGTTTTTACCTATCTAAATAGTGATTCTGTTCACATTTTTGACTTTTTTTACGACAG
Seq C2 exon
GTGGTTCAGCTGACTGTGATGCTGGAAGCTCTGCTTGGGGCACAACCTGATGATCCTGATGTTCTAGAGTGCTTTTTCTTGGAAGCCTTATATTTCTCTTTAGGTGCTTCTCTTCTTGATGCTGGAAGAGTTAAATTTGATAAATACATTAAACATGTTTCCTGTATGTCAACTGTTCATGATGAGAACATCCTGGCTAAGCCAGGGGAGCTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000003170:ENSGALT00000005023:41
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:
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:
CAAGAGAGAATTGAATTGAATCGTTT
R:
CAGCTCCCCTGGCTTAGC
Band lengths:
348-652
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]