Special

GgaINT0049820 @ galGal3

Intron Retention

Gene
ENSGALG00000012495 | Q9DEH4_CHICK
Description
NA
Coordinates
chr7:36815964-36816634:-
Coord C1 exon
chr7:36816542-36816634
Coord A exon
chr7:36816057-36816541
Coord C2 exon
chr7:36815964-36816056
Length
485 bp
Sequences
Splice sites
5' ss Seq
TCGGTATTT
5' ss Score
4.52
3' ss Seq
AATTCTCTTGTACCTCATAGGTG
3' ss Score
7.77
Exon sequences
Seq C1 exon
GTCTTGTACAAAGAGGACCTGGGGACAGGTATCCCAACACCTGTTACTCCAGAAATAGAGAGAGTCAAACGCAATCAAGAACACATTAGCTCG
Seq A exon
GTATTTAAGAAAAAGATGATAACAATTCATTTTTGCATAACATCCTAACATGTACTCCTTTTTTCTTTAGTGATTTAAAATCTCACCTCACCCCACTCCTTTCTTCCCTCTGTCAGTACTTTTAACTTAATTCTTCCACCTTTTTGTGCTTTAACTTTTTGGAGTGATTTACAACTTTACATGCATTTCTTTTTAAGAACCGAAACCTTTATAAGCTGTGAAAACATTCTGGTGTTCCTCCCTGTGTTGGTTTTATCTTAACGCTTTATCTCCTGGGATATGTAGCCATATTTACAGAATAATCAGCCCCTTCCTTAATATTCACCTCTAGAACAAGTGTGCAATTAATGAAAAAGTGACCCTAACGCTAAACATAACTCACAGAATAGTGAGACGTAATTATTTTGCCTGTGTTGAATGCTGGGTTTTTGTATGTTCTTTGTTTGGTCAGGCTTTTTGTATGGAAATTCTCTTGTACCTCATAG
Seq C2 exon
GTGGCATACAAAGAGGGCTTAGGGACGGGCATCCCAACCCCGGTCACTCCGGAGATGGAGAGGGTCAAACGCAACCAAGAGAACATTAGCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000012495:ENSGALT00000020410:132
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.839 A=NA C2=0.968
Domain overlap (PFAM):

C1:
PF0088013=Nebulin=PD(28.0=22.6),PF0088013=Nebulin=PU(64.0=51.6)
A:
NA
C2:
PF0088013=Nebulin=PD(28.0=22.6),PF0088013=Nebulin=PU(66.7=51.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Human
(hg38)
No conservation detected
Cow
(bosTau6)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGTACAAAGAGGACCTGGGGA
R:
CGAGCTAATGTTCTCTTGGTTGC
Band lengths:
182-667
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]