Special

GgaINT0042918 @ galGal3

Intron Retention

Gene
ENSGALG00000023925 | Q8QFT4_CHICK
Description
NA
Coordinates
chr6:17659240-17659964:+
Coord C1 exon
chr6:17659240-17659389
Coord A exon
chr6:17659390-17659803
Coord C2 exon
chr6:17659804-17659964
Length
414 bp
Sequences
Splice sites
5' ss Seq
AGAGTACGA
5' ss Score
2.43
3' ss Seq
TAACTTTGCTGATCTCACAGGAC
3' ss Score
7.03
Exon sequences
Seq C1 exon
GCATTATTTTCAGCAACAACGAGGGATGGTTACACGTTCGGCGGTTTGCTCTCAGCACTCTGCGCAACTTTGGGATGGGGAAGAGGAGCATTGAAGAGAGGATCCAGGAGGAAGCTGAGCACTTGCTTGAAGAGATCACAAAAACAAAGA
Seq A exon
GTACGATCCACTGCTAATACAGCCTACATCTGCAAAAAAGGAACGTGCCAAGGGAGCCCACGTTCTTAGCAGAAGCTAGGGAGTCTCCATTCTTGGAGATACTCAAAAGATGTCTGCACGTGCTCCTGCGGCAGCGGCTCCCGGTGCCCCTGCTTGAACAGTGGGCAAGGTGGTCTCTCAGAAGTCTCTGAGCCCTTCTGTGAGTCTGTTAACGCACCCTACGGTGCATTTCACCCCTGAAAGCTGTTAGCAATGCCATGATTGTGTTCTGTTCTTATGGAGAACCCCTCTGTTTTCATTCAGAGACTGTGAAGTTCCAGTGTCTGCTGCAGCTCATGTTACCCAGAGTAGCCATAGGTCTCATTTAATTCATTCTTTGCTTATTTGTACACTGTAACTTTGCTGATCTCACAG
Seq C2 exon
GACTGCCCTTTGACCCAACATTCAAGCTGAGCTGCGCTGTCTCCAACGTCATATGCTCCATTGTCTTTGGGAAGCGATATGACTATAAAGACAAGAAGTTCCTATCTCTGATGAACAACATGAACAACACATTTGAGATGATGAACTCCCGCTGGGGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000023925:ENSGALT00000008787:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

No protein impact description available

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

C1:
PF0006717=p450=FE(17.2=100)
A:
NA
C2:
PF0006717=p450=FE(18.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg38)
No conservation detected
Mouse
(mm10)
No conservation detected
Rat
(rn6)
No conservation detected
Zebrafish
(danRer10)
LOW PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TTATTTTCAGCAACAACGAGGGA
R:
CCAGCGGGAGTTCATCATCTC
Band lengths:
302-716
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]