Special

GgaINT0008919 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr15:4897521-4898166:-
Coord C1 exon
chr15:4897990-4898166
Coord A exon
chr15:4897644-4897989
Coord C2 exon
chr15:4897521-4897643
Length
346 bp
Sequences
Splice sites
5' ss Seq
GAAGTATGT
5' ss Score
6.97
3' ss Seq
TACAAAGTTTTCCTTTCTAGGTC
3' ss Score
10.11
Exon sequences
Seq C1 exon
GTTGAATATGTTAAACAAATCTTTGTTCAAAACCTCATGGATCCACCCTTATTCAAGAATCATCCTCCACTGGCTGGAGCAATATACTGGTCCCGATCACTTTTCTATCGCATCAAACACACTATTGTTCGATTTCAGGAAGTAGAGGGGTTGCTTGCTAGTGAACGTGGAAAAGAA
Seq A exon
GTATGTTGGTTTCTTTGCTGTTTAATGAAGGAAGAAATACTTTCCTCGCACCTTTCTTCTAGGGATGTGAAAATGCTCTTATGTGAATGAAGTCCGAAGAACGTCTTTGCACGTAGTGGTCCATGTTAGTCATGAAAATTTGATTGGAAACCTTTTCACTGTTTCTCAGAGAGAGAGTGACAGAATCAATGACAGAACTCAAAAACCTAAATTCTTCATTGTCTGCATAAATTACAAGGCATTACCTACCCTCTCATTTAATACAGTTTGGAAACAAATCTTATTAAGACAGGATAGTGAATAATTTTTCCTGATCTTTAAGATGATACAAAGTTTTCCTTTCTAG
Seq C2 exon
GTCAAGCAAATATATCTTAAAGTGGCCAAGAGGATGAAAGAATATGAAGATCAGAAATATGATCAGTGGAGACATGAGACAGAAAAGATGCTCCCACTGTTATTGGAAAAAACTCTGCTGATA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000003170:ENSGALT00000005023:12
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:
PF083857=DHC_N1=PD(0.1=0.0),PF083857=DHC_N1=FE(25.4=100)
A:
NA
C2:
PF083857=DHC_N1=FE(21.5=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:
ATCTTTGTTCAAAACCTCATGGATCC
R:
TTTTTCCAATAACAGTGGGAGCA
Band lengths:
270-616
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]