Special

GgaINT0013864 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:2949]
Coordinates
chr14:14999561-15001004:-
Coord C1 exon
chr14:15000861-15001004
Coord A exon
chr14:15000228-15000860
Coord C2 exon
chr14:14999561-15000227
Length
633 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTT
5' ss Score
7.64
3' ss Seq
TTTTGCGTTGATCCCTGTAGGTA
3' ss Score
9.48
Exon sequences
Seq C1 exon
AGTGAAGACAAGCTGATCCGTCTTTGGATTCATGAGGTGTACCGAGTTTTCTATGATCGCTTAGTTGATGAGGAGGACAGGGAGGTATTCTTTCAGATGGTAAAAAAGACAACATCAGACAGCTTCAAGCAGAACCTTGATAAG
Seq A exon
GTATTTTTCAGCAACATGGTAGACCCAAGTGTTTCAGAAACACTTAGACACTGAGATTGCATTAGCACTGGATATATTTTGAATGATTTATATTGGTGCATTCATAAAGTTTGGATTTTCGTCTGTTTGTATTATGTATTATATGTACTCTTATGGAAACTAATATTTCATATCTGCATGATCCAGAACTTGAAAAGGATTCTGCTTTGGTACAGAGGACTGCGTGGGATAACTGTCGTTCACTGTTCACTTGTGCTCCTGCTTAACATACACTGGAATGAGTTGCTGGGAGTAGTGGGTACTTTTCTGAGAAGCCTTTTGGCAACTTTTCGTGCTTTTCACAGTACAATCACCATGTGAGATGTGCATGGCAGAAACTTGCATGCCTGCTTACAGCATATAACTCTGTTCAGGAGGTTTTTCTGTTTCACCTCTCCACCCTCTTCCACTCTTCCACTCTCTTTTTTTTCTTTCTTTCGTCTTTGTTTCTTTTTTTTTCTTCCATACTAAGATGATAACCAAAATGGCTGGAAAATGGCACTTCCCGCAGTATTATTATTATATGATAAGAATAATTACTGCTTTAACGGAAGTAATTCTCCAGTAGTCTGAATTTTGCGTTGATCCCTGTAG
Seq C2 exon
GTACTGAGTCATCTCTCACCCACTGGCAAGGTCACAGATGATCATATCCGCAGCCTTTTCTTTGGAGACTATCTGAAGCCAGACAGTAATGCAAAAGTGTACGATGAAATCACAGACTTGAAGGAACTGACAGCTGTGATGGAATCCTACCTGGAGGAATACAACAATACCAGCAGAGCACCAATGCCCCTAGTCATGTTCAAGTTTGCTATTGAGCATATCTCAAGGATATGCAGAGTACTGAAACAAGATAATGGACATCTTTTGTTGGTGGGCATTGGTGGAAGTGGTCGACAAAGTGCTACCAAGCTAGCCACCTACATGAGTATGTTTGAACTCTTTCAAATTGAAATTACAAAGTCCTATGGAATCAATGAATGGAAAGAAGATATTAAACGAGTCATGCTAAAGGCTGGTGTTGGTAACAAGAACATTTCCTTTTTGTTCTGTGATAATCAAATAAAGGATGAAGCATTTATAGAAGACATCAACATGCTTTTAAATACTGGTGATGTGCCTAATATTTTTGCTGCTGATGAGAAGGCTGAAATTGTTGAGAAAATGCAAAGTGCATCAAGGATGGGGAGTGAGAAAATTGAAGCTACTCCGCTTGCTATGTACAATTTCTTTATTGAAAGGATGAAGAAAAATTTACATATTGTCTTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002350:ENSGALT00000003708:46
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=0.000
Domain overlap (PFAM):

C1:
PF127752=AAA_7=PD(4.1=22.9)
A:
NA
C2:
PF127802=AAA_8=PU(62.6=75.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTGATGAGGAGGACAGGGAGG
R:
GCCCACCAACAAAAGATGTCC
Band lengths:
356-989
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]