Special

RnoINT0138475 @ rn6

Intron Retention

Gene
Description
solute carrier family 4 member 3 [Source:RGD Symbol;Acc:3712]
Coordinates
chr9:82750729-82751391:+
Coord C1 exon
chr9:82750729-82750923
Coord A exon
chr9:82750924-82751172
Coord C2 exon
chr9:82751173-82751391
Length
249 bp
Sequences
Splice sites
5' ss Seq
AAGGTGTGG
5' ss Score
5.28
3' ss Seq
CTCTTCTTCTCCACACATAGGTG
3' ss Score
8.97
Exon sequences
Seq C1 exon
TTCTGCCGAGCTCAGGACCTGGAATACCTCACCGGTCGAGTGTGGGTGGGCCTCTGGCTGGTGGTCTTCGTCCTGGCCCTGGTGGCGGCTGAGGGCAGCTTCCTTGTCCGCTACATCTCGCCATTTACCCAGGAGATCTTCGCTTTCCTCATCTCACTAATTTTCATCTATGAGACTTTCCACAAGCTCTATAAG
Seq A exon
GTGTGGTAGTGTCCAAGAGGGTGAGTAGGGATAGGGTGGAGGTGGTGTCCCAAGGAGACTTGGAGCTTGATGAGAGAAGACATAGGGAAAGGGGCTTCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACATGTGCATGTGTACTGTCTTGGGAGGTGGGGATTAAGGGACACCAGGGCTGGGTTTGTTATCTGCCTGTGGAGAGTGAGGCCTCTTCTTCTCCACACATAG
Seq C2 exon
GTGTTCACAGAGCATCCTTTGCTGCCCTTCTACCCACCGGAGGAGGCCCTGGAGCCTGGCTTGGAACTGAATAGTAGTGCCCTGCCCCCCACAGAGGGACCACCAGGTCCCCGGAACCAGCCCAATACAGCTCTGCTGTCCCTCATCCTCATGCTGGGGACTTTCCTCATTGCCTTCTTCCTGCGAAAGTTCAGGAACAGCCGCTTCCTGGGGGGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000020138:ENSRNOT00000027337:16
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=0.164
Domain overlap (PFAM):

C1:
PF0095516=HCO3_cotransp=FE(32.5=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=PD(12.2=32.9),PF0095516=HCO3_cotransp=PU(19.7=80.8)


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:
AATACCTCACCGGTCGAGTGT
R:
GAGCTGTATTGGGCTGGTTCC
Band lengths:
306-555
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]