Special

RnoINT0102270 @ rn6

Intron Retention

Gene
Description
notch 3 [Source:RGD Symbol;Acc:620761]
Coordinates
chr7:14176456-14176970:-
Coord C1 exon
chr7:14176737-14176970
Coord A exon
chr7:14176567-14176736
Coord C2 exon
chr7:14176456-14176566
Length
170 bp
Sequences
Splice sites
5' ss Seq
CAGGTTTAT
5' ss Score
4.29
3' ss Seq
TTCCTCCTCCCCTGTTGTAGGTG
3' ss Score
11.11
Exon sequences
Seq C1 exon
GCTTTGAGGGCACCCTGTGTGAGCGAAACGTGGACGACTGCTCTCCGGATCCCTGTCACCACGGGCGGTGTGTCGACGGCATTGCTAGCTTCTCATGCGCTTGTGCGCCAGGCTACACGGGCATACGCTGCGAGAGCCAGGTGGATGAGTGCCGCAGCCAGCCCTGCCGATACGGGGGCAAATGTCTAGACTTGGTGGACAAGTACCTCTGCCGCTGTCCTCCCGGAACCACAG
Seq A exon
GTTTATTTTATTTTGTTTTTTTGGGTTTTTTTTTTTTTTTTTTGTTTTTTGTTTTTGAGGGGACTGGGCTCTGACAGTACATGGGGGTGTGTGGGTGTCCGTGATGAGTTTGCAAGGGTTGCTTGATGATAGCCCTTACTCCTGCCATACTTCCTCCTCCCCTGTTGTAG
Seq C2 exon
GTGTGAACTGCGAAGTCAACATCGATGATTGCGCCAGCAACCCCTGTACCTTTGGAGTTTGCCGTGATGGCATCAACCGCTATGATTGTGTCTGTCAGCCTGGATTCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000004346:ENSRNOT00000037456:11
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:
PF0000822=EGF=PD(16.1=6.3),PF0000822=EGF=WD(100=38.0),PF0000822=EGF=PU(90.3=35.4)
A:
NA
C2:
PF0000822=EGF=PD(6.5=5.3),PF0000822=EGF=PU(90.0=71.1)


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:
GAAACGTGGACGACTGCTCTC
R:
TGGCGCAATCATCGATGTTGA
Band lengths:
246-416
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]