Special

GgaINT0129356 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr18:394092-394885:-
Coord C1 exon
chr18:394812-394885
Coord A exon
chr18:394180-394811
Coord C2 exon
chr18:394092-394179
Length
632 bp
Sequences
Splice sites
5' ss Seq
AGGGTAAGT
5' ss Score
10.45
3' ss Seq
ATTTGTTCTTGCTTCCACAGGAG
3' ss Score
10.76
Exon sequences
Seq C1 exon
AGAGTGGTGGTGGTGGCAAGAAGGGAGGCAAGAAGAAGGGTTCTTCTTTCCAGACTGTATCAGCTCTTTTCAGG
Seq A exon
GTAAGTACAGAAGTAATTGTCTCTTGATCTTTCTCATTTTACTGAACCTGTTAACATTTTTCTTTGTATCAAAAACATATTTTAAGTTATTCATGAAAGGGCTAACTTCAAGTCAGATGAGGCCAGGGGAAAGATAGATACTGATTTAGTCTCTCCTTGAATGTTTGAAAAAGTAGCCTAGGTCAGGCTACAGTTTCATTTAATTATATGCATGTGGGTTAGTAGGACTAAGCTCTCTTCTGTCCTGGAAGGACAATGGTGGATATGGATGTCTGTCTGAAGGAGTGTCTAGTCTGGATCTGCACATGCATTTGCAAATGAATATACACATGAAGTCAAAGCAATAGGGAAATGCCAACACCAGCTATCACCCCTCCACAGTGTAAGGCAGATGGAAACACTCTTATTTGAACGCTAGATATGATCTGGCATCCCGTACAGTTTTTCATACTCAACAGCTTTGCCATTACTCCAAACCAGGACTTCAAGACTAAAAACTATTAAAAACCTCAAATTGGTATGGTACTACATGGGAATATCAAGTCCATTATTCCTTTACAACAGCTCCAATATCTCACAGAACTGCAGAGTTAACATTTGTTAATGAAAAACATTTGTTCTTGCTTCCACAG
Seq C2 exon
GAGAACCTGAACAAGCTGATGACCAACCTACGGAGCACTCACCCCCATTTTGTGCGCTGTATCATCCCTAATGAAACAAAAACTCCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000023867:ENSGALT00000001420:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.400 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(3.5=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.2=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]