Special

RnoINT0121162 @ rn6

Intron Retention

Description
pregnancy-zone protein [Source:RGD Symbol;Acc:628643]
Coordinates
chr4:161811340-161811976:-
Coord C1 exon
chr4:161811820-161811976
Coord A exon
chr4:161811415-161811819
Coord C2 exon
chr4:161811340-161811414
Length
405 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
TTCTCCTTCCATTCTTCCAGGGT
3' ss Score
10.66
Exon sequences
Seq C1 exon
GCTCACTGCATTTGTGCTCAAGGCCTTCGCTCAAGCTCAGTCATACATCTATATAGAAAAGACACACATCACAAATGCTTTCAATTGGCTCTCGATGAAACAAAGGGAGAACGGTTGTTTCCAACAGTCTGGATCCCTGCTCAACAATGCGATGAAG
Seq A exon
GTGAGGCCCTGCTAGCGTCTCTGCGAGACTCTCGAGGTTGTGATACATAGGAAGGGAGGCCTCTCTAAGAGTTCTCCGGTCCTTCAGGCTGGAGAGATGAGTCCACAGTTGAGAGTGGTTAGTGCTATTGCAGAGGATCTATTTGGTTCCCAGCATCCTTCCACCCATTTCTAACCAGCTCCACATGACCCAATGCCTCCCTCTTCTGGCATCAGTGGGTACTGCATTCATGAACGAACCCACATATAGATACACACATATATACGTGATCTTACAATCTTAAAAGAAAAAGAAAAGAATTCTCCAGTCCTGATGACATAACTCAGAGGGTCTAATGCTTTTAACAAAGACTTAGCAGACCAGCAAAGACTGAGGTGTGTGAGCGTTCTCCTTCCATTCTTCCAG
Seq C2 exon
GGTGGTGTGGATGATGAAGTGACACTCTCTGCCTATATCACCATTGCTCTGCTGGAGATGCCCCTGCCTGTCACT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000006709:ENSRNOT00000009467:26
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:
PF076789=A2M_comp=FE(19.5=100)
A:
NA
C2:
PF076789=A2M_comp=FE(9.0=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:
GCTCACTGCATTTGTGCTCAA
R:
TGACAGGCAGGGGCATCTC
Band lengths:
230-635
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]