Special

RnoINT0130046 @ rn6

Intron Retention

Gene
Description
retinoid X receptor alpha [Source:RGD Symbol;Acc:3610]
Coordinates
chr3:6291967-6293532:+
Coord C1 exon
chr3:6291967-6292058
Coord A exon
chr3:6292059-6293426
Coord C2 exon
chr3:6293427-6293532
Length
1368 bp
Sequences
Splice sites
5' ss Seq
CTGGTACGG
5' ss Score
8.6
3' ss Seq
GAGGCTGTTTTCCTCTGCAGACT
3' ss Score
8.93
Exon sequences
Seq C1 exon
GGTGCTAACGGAGCTGGTGTCGAAGATGCGTGACATGCAGATGGACAAGACGGAGCTGGGCTGCTTGCGCGCCATTGTCCTCTTCAACCCTG
Seq A exon
GTACGGCCCTGCCATCTCCTCTGTGGGCCTTCGGGGCCCAGCGTCCCCATCACAGAAGACACCAATCTCCTGCCTCCACTTGTCTGGAGACTTAATGGAGAGGCTCAAGTGGCACTCTATGAGACTGGAGTGTGCACTTGACATCAGTGCTCTCCGGCTGAGCCTCGCGGGCTCTGCTGTCCACAGTGGTCTTCCGTTAGAGTGAGCTCCCAGGATGGGGTTGGTGGTCAGTCCATCTTGTTAGGTGTCCCGAGGGTGGCTGACATGTCTCAAGCCTTGGTTTGAAGGGCGTTTGGGGGGGTCAGGGTGGAGTAGCCTCTTGAGGACAGCAAGCCCCTTGGTTGGCTCTGGAGCTTCAGTGTGCGGGGCCTCCAAGCTGCTGCTGCCACAAGGCTGAGGCAGTGTCTTCTGTGTGGGACGCTGCATGCGAGGCTGGAGTGTGAGCAGTGGCCCAGGCCCGTGCTCACAGCACTGGGTGGGTGGCAGATGCCACTGGTGGCCAGTTCACATGGGGATGGGAACGCATTAGCAGAGAGTGTGGGATTCTTGCTGAGAAGAAGCTCAGGGATTCAAGGGGTGGCCCATGGACTTGTGGATGCTCTGGCCAGGCTCTAGGAAGCGCTGGGCACTTGCTGCAGCAGGCATTCATGGGCTTCCGTATTTGAAAGTTCATCCCTGTCTGCCTAGGAAGGGGTTGAATGTGGGTTGGGAGCTTGGCTGATGGGGCTCACCAGCCCTGCCCATAGTGAGTAGAAGATATGGGGGGACAGGGACATAGGCTTCCACCCCAGATAGCTCACCAGGCTGTAATTCCTGAGCCAACCTCATAGTTTCCCAGGTTAGGTCTGAGTAGGAGGTATGGCGAACCAGGGACGCTTGGGCCTGGGGCCTCAAGGGGTAGGGAGGGGTAGTCCTGTCAGGACTGGGTCAGTTGAAGGTGTCTTATGTAGTCTAAGCTACCCCCAGCATTCTTACTGGCACAGTGGGCCCTGATGGTGTTGATGACTGTGGTTGTGGCTTTCCTGCAGCCTGTATTGTGGCCAGTGTCTAGGTTCTATGGAGGAGCCTCCCCGACTCATGGTGTGGGGAGATCCTCAGGGAAGGGCTTCCTGTCACTGGGGCCAGGGCCCAAGGGCAGTAAAAGCATTGGCCATGGCCACCTAGAGAAAGGTGGGGAAACTAAGTCCTCTAATGACAAGGTCACTTGACTTTCAAGTGGCCGAGTGGAGCACCCGTCCTCCTGGTTTCGGAGCTCTGGGTCTGCAGGGCAGCCATATCTACTTGTGTAGCATATGCCCTCTCTGCTGGGCTTGCATGTTTGTGGGAGGCGGTCTGGGGGCTCTGACCTGAGGCTGTTTTCCTCTGCAG
Seq C2 exon
ACTCTAAGGGGCTCTCAAACCCTGCTGAGGTGGAGGCGCTGAGGGAGAAGGTGTATGCATCACTAGAAGCGTACTGCAAACACAAGTACCCTGAGCAGCCGGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000009446:ENSRNOT00000012892:8
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:
PF0010425=Hormone_recep=FE(16.1=100)
A:
NA
C2:
PF0010425=Hormone_recep=FE(18.2=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:
CTAACGGAGCTGGTGTCGAAG
R:
CCGGCTGCTCAGGGTACTT
Band lengths:
190-1558
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]