Special

RnoINT0131070 @ rn6

Intron Retention

Gene
Description
SR-related CTD-associated factor 4 [Source:RGD Symbol;Acc:727896]
Coordinates
chr11:30406465-30407277:-
Coord C1 exon
chr11:30407194-30407277
Coord A exon
chr11:30406510-30407193
Coord C2 exon
chr11:30406465-30406509
Length
684 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
3' ss Seq
TTTTGTTTTTTTTTTTTCAGCTT
3' ss Score
11.08
Exon sequences
Seq C1 exon
CTCTTCTCACTTATGGATATGAAACCACCCATCTCTAGAGCCAAGATGATTCTTATTACTAAAGCTGCTATTAAAGCTATTAAG
Seq A exon
GTAAGAAAAATATTTAATTTAGGAATACTTTTAATTGTTTAGTTAATTATTGGTGGCAGAGGTAGGGCATGAGGTGGTACGCACGTGGAGGTTAGAAAACCACCTTGAAAGTTCTCTTCCACCTTTACCTGGGATCTAGCTTAGTTTGCCAGCTTTCTATAACAAACATCCTTACCTACTGAGCCATCTTGCCAGCTCTGCTTTGAATTTTTTTTTTTTAAGTTTGTTAAACATCAGAATTTATCTTGTGAATTAAGTTTTGCTGAAGGTTTTTGGTACTACTGTGCATTTGCATTGTGACATCTATTCACAGCACTTTGCCATATTTCAATCCTTATAAACCAGCTTGTGGGGAAGGGGGAAGTCAAGACTTGGGCTATGTTACCCAAGCTCACATTTGAGTGAATGGCACAGTTAAGAAATAGTATTACTTAGTTTTGGCTCTGTTTCTGTCCCTAGTGAAATAACCTCATACCTTGATACATGAAGATTGATGAAGGAGTGTGTAGTCTTGTTTTGATTAATTCCTTTCTCGGGATTCTAAAGTTGTTGATTGTGAACTATTTCTAACGGCTCTTTGGGATAATTGCTAATTCTTTTAAGTTGGACATTTCAGGGTTTTGAATTGTGGAAAATACAGACATGTATAAACCGACTAATTTTGTTTTGTTTTTTTTTTTTCAG
Seq C2 exon
CTTTATAAGCATGTTGTTCAAATAGTAGAAAAGTTCATCAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000002104:ENSRNOT00000002881:4
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Mouse
(mm9)
No conservation detected
Chicken
(galGal4)
ALTERNATIVE
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]