Special

GgaINT1011511 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr18:10085504-10085953:+
Coord C1 exon
chr18:10085504-10085711
Coord A exon
chr18:10085712-10085787
Coord C2 exon
chr18:10085788-10085953
Length
76 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAGG
5' ss Score
9.16
3' ss Seq
ACGCTCTCCGCCCTTTGCAGCCA
3' ss Score
8.75
Exon sequences
Seq C1 exon
GCCTCCATGGTGCACACCACCGAGACCGTCCGCATCCGCTACTTCATGGACCTGCTGATGGAGAAGCAGCGGCCGGTGATGCTGGTGGGGAATGCGGGCACGGGGAAAACTGTGCTGATGTGGGACAAGCTCGAAGCTCTCAACACAGAGGAGTACCTGGTGCAGTCTGTGCCTTTTAACTTCTACACCACCTCTGCCATGCTGCAGG
Seq A exon
GTAAGGGCCGCCCACAGCTGCCTCTTTGGGGGCTCCGTTGTGCTTCCCCATGGCCCACGCTCTCCGCCCTTTGCAG
Seq C2 exon
CCATTCTGGAGAAGCCTCTAGAAAAGAAGTCGGGGAGGAACTATGGCCCACCAGGCACTAAGAGGCTCATTTACTTCATTGATGACTTGAACATGCCCGAGGTGGACAAGTATGGCACTGTGGCTCCGCACACACTCATCCGGCAGCACATGGACCATGGGCACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007106:ENSGALT00000011513:46
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=0.089
Domain overlap (PFAM):

C1:
PF127752=AAA_7=FE(25.4=100)
A:
NA
C2:
PF127752=AAA_7=FE(20.2=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:
AGGAGTACCTGGTGCAGTCTG
R:
GTGCCATACTTGTCCACCTCG
Band lengths:
178-254
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]