Special

RnoINT0138488 @ rn6

Intron Retention

Gene
Description
solute carrier family 4 member 3 [Source:RGD Symbol;Acc:3712]
Coordinates
chr9:82746826-82747500:+
Coord C1 exon
chr9:82746826-82747006
Coord A exon
chr9:82747007-82747364
Coord C2 exon
chr9:82747365-82747500
Length
358 bp
Sequences
Splice sites
5' ss Seq
AGGGTAGGG
5' ss Score
5.76
3' ss Seq
TTTCCCTCACTGTGTCCTAGGAG
3' ss Score
9.01
Exon sequences
Seq C1 exon
GTGTTCGTGGAGCTGAATGAACTGATGTTGGACCGGAGCCAGGAGCCACACTGGCGGGAGACAGCACGCTGGATCAAGTTCGAAGAGGATGTGGAGGAGGAGACAGAGCGCTGGGGGAAGCCTCATGTTGCTTCGCTCTCCTTCCGTAGCCTCCTGGAGCTTAGGAGGACCATTGCCCAGG
Seq A exon
GTAGGGCTCCTTGGGCTGGCCCTTCTCCCCACCGTAGCTCCATCTGTGTTGGGCTGCCCAGTGTGCCGGGATCATTTGGGGAATTCTGAGGGGCAGGACTACACATTGCACCTGGGCCTAATGGACGGCCTTCTAGCTGTCTGCACTCTTAGGGTATGACTCCCATTGCTCGGCTCCTTGTGCCTCAGCCCCTCGCACACCATTTTCCATATGCTCCTCCAGATGCCTGTGAGGTGTGTAACTGCTGTTAGTGCATTGGCCCTCAGCTCACTTTACACATTGGCCTGCCCTTGGGGAGCAAGGTAGTGGGGTGGGCCTCCCTTCTGGCCGGACGGCTCTTTCCCTCACTGTGTCCTAG
Seq C2 exon
GAGCGGCTCTCCTGGACCTGGAGCAGACCACCCTGCCGGGCATCGCTCACCTTGTGGTGGAGACCATGATTGTATCTGACCAGATCCGGCCCGAGGACAGGGCTAGCGTTCTGAGAACTCTGCTCCTGAAACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000020138:ENSRNOT00000027337:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.082 A=NA C2=0.130
Domain overlap (PFAM):

C1:
PF075658=Band_3_cyto=PU(11.5=50.8)
A:
NA
C2:
PF075658=Band_3_cyto=FE(16.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCGTGGAGCTGAATGAACTGA
R:
TGTGTTTCAGGAGCAGAGTTCT
Band lengths:
312-670
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]