Special

DreINT0049827 @ danRer10

Intron Retention

Gene
Description
collagen, type IV, alpha 5 (Alport syndrome) [Source:ZFIN;Acc:ZDB-GENE-030131-2281]
Coordinates
chr7:50889160-50890833:+
Coord C1 exon
chr7:50889160-50889325
Coord A exon
chr7:50889326-50890740
Coord C2 exon
chr7:50890741-50890833
Length
1415 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
ATGTTTGTTTTTATGAATAGGTC
3' ss Score
8.91
Exon sequences
Seq C1 exon
GGTTTGGGACTGAAAGGTACACAAGGTCCCAACGGTGAACCTGGTTTGCCAGGACCTCCTGGAGACAGAGGTTTACCAGGTTCCCCAGGATTTGGTCCTCAAGGACCTTCTGGAGAAAAAGGTATTCAGGGTGTTTCAGGAAGACCAGGGGCACCTGGACTACCAG
Seq A exon
GTAAGAAACAATGCAATGTTTATTTAAAGTTTTCTTTACTTTAAAGAGCCCCTATTATACATTAAAAAGGTCATATTTTGTTTTTGGAGGTCTCCAAACATTGTCTTATAATATGCATTCATTTTTACCTAATTATCCCAGCGATTCATTTATTCCCAAACCCCTCCTAATCTGGGCTGATTGGACGGATGACAGTCTGTTGCGATTGGTCGACAGCGTTCAGTATGAGACAGAGTAAAATGCCCACCACGGCTTATCAACAATATTGAATTAGTCAGAGTGCGTAGTGTATGTGTGCGCATACCTGCCAACACTCCTGTTTTTTCCTAGAGTCTCCCGTATTTCAGACCCATCTCCCGCCTCCCTCCTGTTTTGGTATTTATCCCGGAAAACGCCCAAAATTTCAACCCCCACCACCCACGAGCTCTGACAAAGTCCCACTCACTAATAGTTTTTTCAGATCCTTCCTTTAACAAACGGCCGATGAATCCCCCTTTGTAAATGTGTAGACTGCAGAAGCACTCGTCAGAAAAATGACGGGAACACAGCACAAGGCTGGGGCTATAACGCTGAGGAATTTTTGCAAAAATAAACCTAAACCACTGACTCTTCACAGTTTCTTCTTTGGGTAGTGAAAATAACACTAACTTTACCTTACACTTCCGAATATATTCAGCAGAGCACAGCATCTTCACAACTTTATTTAACAGGGATCTGCTACAGTGCGTGTCTTCCTCTTTTTCTTTGCTACTGTATTTGTGGGCAGGGCTGAGGGTTTAAATTTTCCTAGGTTTGCGTGTGCAATAATTGAAATGGGCTTAAGTTTCGTAACAACATCACACTGACACTTGTTATCAAGACGATTCATTTGAAGCACTCTGAGTCAACTCTTTTTTAGACAAATGAAACACTGTGCACTTTCAGATTTAAGCCATAGCTGGATATTTCACTTCACTTAGAGGTGTGTTACCAATGCCATTTGTTATTTTGTTGTCATTTTAAAAAAATAATAATAGGGGCTCTTTAAGGATCTTATTCAGTTAAAATGCAGTTTATATAAAATGCATATAGGCTATTTTCTGCTCCATTCAAGGTAAATATCTACTGTAGATTAGTCTTGAAAATCTAGATGGCACAGAATGATTGCCCTCTGTATCCAATCAGATTTCTTGCTGAACATTTAAATACTATGATTGAGTTGTCATAGCCAATAGAGCAGTAGAGTAATCTGCTGTAGCTGCATGTGCAAATCTAATCCTACAAGGCTAAATGCATTTACATTGTCTTAATTATTAACATGACACACCCTTCAGAGTTTTTGACAGCTTATTTTCTTATGGAGTGCATTTTTTGTAGCTTTCAGTTTGGTAGTGTTCTACTATAGACATTATCTCAATGTTTGTTTTTATGAATAG
Seq C2 exon
GTCAGAAAGGTGAACCTGGGATGACTGTGCCAGAAGTTGGTGAACGTGGACCCCCAGGACAGGATGGAGATCCTGGTTCACAAGGACGTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000052063:ENSDART00000073827:25
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(20.8=19.6),PF0139113=Collagen=PU(82.8=94.6)
A:
NA
C2:
PF0139113=Collagen=PD(15.6=31.2),PF0139113=Collagen=PU(46.9=71.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TGGGACTGAAAGGTACACAAGG
R:
CTGGACGTCCTTGTGAACCAG
Band lengths:
255-1670
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]