Special

RnoINT0138596 @ rn6

Intron Retention

Gene
Description
solute carrier family 4 member 9 [Source:RGD Symbol;Acc:628811]
Coordinates
chr18:29359651-29360074:+
Coord C1 exon
chr18:29359651-29359812
Coord A exon
chr18:29359813-29359895
Coord C2 exon
chr18:29359896-29360074
Length
83 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
3' ss Seq
ACAACCCCCATTCCCTGCAGAAG
3' ss Score
8.61
Exon sequences
Seq C1 exon
CCTACACTCCCTGGGCGTGGCTGGCTGGTGTCTCCTTTTGGAGCTAACCCCTGGTGGCTGAGTGTGGCTGCTGCCTTGCCTGCTCTGCTGCTGTCTATCCTTATCTTCATGGACCAGCAGATCACAGCGGTCATCCTCAACCGTGCAGAATACAGACTGCAG
Seq A exon
GTAAGGCTGCCTGCCGGGTAAGGAACTCCAGGGTGGGGTCCAGACTCCACTGCTAGCCTCAGTACAACCCCCATTCCCTGCAG
Seq C2 exon
AAGGGAGCTGGCTTCCACCTGGACCTCTTCTGTGTAGCTGTTTTGATGCTGTTTACATCAGCGCTTGGGCTGCCATGGTATGTCTCAGCCACTGTCATCTCCTTGGCCCACATGGATAGTCTTCGGAGGGAGAGCAAAGCTTGTGTCCCCGGAGAAGACCCCAACTTCCTGGGCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000018525:ENSRNOT00000025137:15
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:
PF0095516=HCO3_cotransp=FE(10.3=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(11.5=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:
TGCTCTGCTGCTGTCTATCCT
R:
GTGGCTGAGACATACCATGGC
Band lengths:
174-257
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]