Special

GgaINT0049741 @ galGal4

Intron Retention

Description
NA
Coordinates
chr7:34746245-34747107:-
Coord C1 exon
chr7:34747003-34747107
Coord A exon
chr7:34746353-34747002
Coord C2 exon
chr7:34746245-34746352
Length
650 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
TTGTTTAATTCTTCACTTAGAAA
3' ss Score
5.79
Exon sequences
Seq C1 exon
CGTTTGTATACTGAGGCCTGGGATAAAGACAAGACACAAATTCACATAATGCCTGACACACCTGAAATCACACTGGCAAAACAGAATATGCATAACTACAGCGAG
Seq A exon
GTGAGTATGTTAGATCTCCATAGGTTCTGTGTCAATATTCTTATAAACCTAATGCAGATATTTTTATAGATCAATTTCTTTAAGTAACACCAAATATCTGTAATCAAAATTGTGGCTTTAGAAGCATAATTTGTAATACATCTGTGATCTCTGCTTTGAATAATTCTATGAAAACTGTGTCTATGGTGAATTCTGGGGTGTTCTTTCTGCCATGATAGATATTGCTAGAAAAGTGCAAAATTCATTCCAACGTTAGAGATGCAAAAAAAAAAAAATCCTTCACAATTGTGATGATTATTGTTCCCAGTGTTCAGTGTTAGTTTAGGCAGAAATATTCACATCAGTGGGAGGTGGCTTTAGAAAGCTTTATTCTACTTGTAATTGAAGGAATAGTTTATCAAGTTGTAATCTATGTCATGTTATTAAAGTTTAGAAAGAAAAAGATTATTAGTGTATTTAGCAAAGATCTTCGTTCAGTATAGATTCATATGAGTTACTGATCTGGAGATTTGAACTAAGGAAGTTAGATAAAACCAGGATAGAATAAATCTTAACAATTTTTTTTACCTACTCGCATGCAATTTGTTTTGCACAGAATGCAGTATATGGAGTTTAGCTACATTAATCCTGTTGTTTAATTCTTCACTTAG
Seq C2 exon
AAACTGTACAAGCAAGCCATGGAAGAAGCAAAAAAGAAAGGCTATGATTTGAGAAGTGATGCTATCCCAATTCAGGCTGCCAAAGCATCCAGGCAAATTGCCAGTGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000028654:ENSGALT00000020410:43
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.200 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0088013=Nebulin=PD(37.9=31.4),PF0088013=Nebulin=PU(55.2=45.7)
A:
NA
C2:
PF0088013=Nebulin=PD(37.9=30.6),PF0088013=Nebulin=PU(55.2=44.4)


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:
CGTTTGTATACTGAGGCCTGGG
R:
GCAATTTGCCTGGATGCTTTGG
Band lengths:
206-856
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]