Special

DreINT0049831 @ danRer10

Intron Retention

Gene
Description
collagen, type IV, alpha 5 (Alport syndrome) [Source:ZFIN;Acc:ZDB-GENE-030131-2281]
Coordinates
chr7:50893443-50893816:+
Coord C1 exon
chr7:50893443-50893593
Coord A exon
chr7:50893594-50893702
Coord C2 exon
chr7:50893703-50893816
Length
109 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGAG
5' ss Score
6.38
3' ss Seq
ATTTTTATTTGTGAACTTAGGTG
3' ss Score
6.29
Exon sequences
Seq C1 exon
GGAGATCCTGGTTATGGTCTGCCTGGTCCTCCAGGTCCCACAGGATCACCAGGCATTAAAGGTGGACCCGGTCCGAAAGGTGATTCTGGTTTCCCTGGAAGCCCTGGTCAACCAGGCCGCCCAGGTCTCGATGGGGCTCCTGGACCTAAAG
Seq A exon
GTAGAGAATTATTTCATGTTCAAACAGAAATTAAATAGTAATGCTGTTCTCAACTCCACTGAAGATGCTGGAATCATCTAAGACTTGACATTTTTATTTGTGAACTTAG
Seq C2 exon
GTGATGCTGGTTTTCCTGGTGGTCCTGGTCCTCGTGGCCCCCCTGGGGCTCCTGCTTTTGGTCTTCAGGGCCCTCCTGGTCCTCCTGGAGCTCCAGGCTCTATTGGATCTCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000052063:ENSDART00000073827:29
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0139113=Collagen=PD(10.2=9.8),PF0139113=Collagen=PU(70.8=90.2),PF0139113=Collagen=PU(8.5=11.8)
A:
NA
C2:
PF0139113=Collagen=PD(27.7=46.2),PF0139113=Collagen=FE(53.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TTATGGTCTGCCTGGTCCTCC
R:
GAGATCCAATAGAGCCTGGAGC
Band lengths:
251-360
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]