Special

DreINT0150950 @ danRer10

Intron Retention

Gene
ENSDARG00000040257 | slc38a11
Description
solute carrier family 38, member 11 [Source:ZFIN;Acc:ZDB-GENE-050417-122]
Coordinates
chr9:50329221-50329685:+
Coord C1 exon
chr9:50329221-50329382
Coord A exon
chr9:50329383-50329572
Coord C2 exon
chr9:50329573-50329685
Length
190 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAT
5' ss Score
8.88
3' ss Seq
TCTGGTGTTTCTTGTTGAAGGTG
3' ss Score
7.44
Exon sequences
Seq C1 exon
CTTTAATCTGCCACCATAACAGCTTCATGATCTACGGGTCGCTGCAGGAGCCCACCCTGAGCAGGTGGTCTCTCGTCACACACATATCCGTGGGCTCATCTGTACTGGTCAGTGCTGTCTTTGCTGCAGCAGGTTATGCCACTTTTACTGTTTACACACAAG
Seq A exon
GTAAATATTTCACAATATAGATTTAAATAGGAAATACTGTGACAAATTTCTTTCTCTGTTAAACATCATTTGGGAAATATTTGATAACGAAATCACAGGCAGGCGAATAATTTTGATTTCAGCTGTATATGTGACAAATTGCACTGGAAGAACCTGAACCTGAATGTTTTTCTGGTGTTTCTTGTTGAAG
Seq C2 exon
GTGATATATTTGAGAACTACTGCAGGTCTGATAACTTGGCTACATTCGGCCGGTTCTGCTATGGTGTCAGTATAATCACTACATTTCCTCTGGAGTGCTTTGTAACACGTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000040257:ENSDART00000058892:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0149013=Aa_trans=FE(13.8=100)
A:
NA
C2:
PF0149013=Aa_trans=FE(9.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
GCTTCATGATCTACGGGTCGC
R:
TCACGTGTTACAAAGCACTCCA
Band lengths:
253-443
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]