MmuINT0122231 @ mm9
Intron Retention
Gene
ENSMUSG00000059481 | Plg
Description
plasminogen [Source:MGI Symbol;Acc:MGI:97620]
Coordinates
chr17:12584615-12586059:+
Coord C1 exon
chr17:12584615-12584735
Coord A exon
chr17:12584736-12585940
Coord C2 exon
chr17:12585941-12586059
Length
1205 bp
Sequences
Splice sites
5' ss Seq
CAAGTAAGG
5' ss Score
7.66
3' ss Seq
AATCCTTCTTGTCCACCCAGATT
3' ss Score
7.9
Exon sequences
Seq C1 exon
AGGAATGCATGTACTGCAGTGGAGAAAAGTATGAGGGCAAAATCTCCAAGACCATGTCTGGACTTGACTGCCAGGCCTGGGATTCTCAGAGCCCACATGCTCATGGATACATCCCTGCCAA
Seq A exon
GTAAGGTCCTGCAGCCAAGCCTGGGGCTTTTTAGATATGCACTCCTCTTGAAGCAAGCAGAAACATCTGAGGAACTGAAGGCTGGGTGGCTTTGATTTTCAAGGCGGGTATCCTCCCGCTAGGCTGCATATAAAGTATGTGTTCTTGTTACTCATCACATGGTCCAGAGGCATGGGTACTTGCTAGAAAGGCAGCATCCAAGCCTTATGAATCGAATTCGAGTTATAACCAAATCCACGGCCAATTTGTATTTCTGGGAAAACGGAGACGCACACTTGGCTTGTTTATGCTCCCTTGCTCCCTTTCTCTCTACACCAGGTATGGTCTAGGTGTTCCAACTGTGATCTATAGCTATCAAGCATCTTACAGATCCCCGATATTTTATTTGTATTTACACCGAGTCATTCACAACTTCTAATCATGTTCTCAACGGTGATTATGAGTTTAAGACAGGACCAGAGGCTCCCTGCTTCAGAAAGCAAGGATGGTTTTCAGAGCAAGCACTTGTGAGGGTTCAAGGTCATTTTTTCCCCCCACAGGAAAACATCTCCCTAGAGATGTCATCCTCTTACGCCTCTTTCTGTGATGACCCTGATGTCATAACAGGGCTACTAAGACTCTCAGTAGCATGGCTAAGCCACGGCTGTCCCTGTGGACAATGGCATTGCTGAGTTTTGCATCTTCTGAAGAGCTTAAAACATGGCTCCTGCCACTGCCTTTCAAAGGCAAGCACAATAATATCCTCAAAGTATGACTAGGTCAAGCCAACTGTAGAACCCAGAAGAGGGGCAATAGACCATTGCTAGCTTTCCTCTTTGTCCTAAGCACCCAGTCTCAGAGAGGAACCAGGCACAGAGACAATCTCCCAGTTAAACCCCTGGGTTCCTGTCAAGGAGGGCTCTCTGGCCAGGTGCTTGAAGGAACATAGCTCCCAATCTTGGATTCTCTAAGCTTCCTGGTAGTGGATAGGTAGACCAGTAGGACTAGGCATCAATTTCCTGCCTGCACCATGTCACTGTCTGAAGACAGTTGCTGGGAAATGAACTCAGGACCTCTAGAATAGTTGGAGCTTGTAACCACTGAGCCATCTCTCTGTAGTCCCTATATGAGTTTTTTATTTCTAAATTATTGATATGTTATCACAGCAAATAAAAAAATGAAAGAAAACAGGAGTTAAAAAAACCAAATCCTTCTTGTCCACCCAG
Seq C2 exon
ATTTCCAAGCAAGAACCTGAAGATGAATTATTGCCGCAACCCTGACGGGGAGCCAAGGCCCTGGTGCTTCACAACAGACCCCACCAAACGCTGGGAATACTGTGACATCCCCCGCTGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000059481-Plg:NM_008877:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.049 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0005113=Kringle=PU(48.7=92.7)
A:
NA
C2:
PF0005113=Kringle=PD(50.0=95.1)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CATGTACTGCAGTGGAGAAAAGT
R:
AGCGGGGGATGTCACAGTATT
Band lengths:
230-1435
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Pre-implantation embryo development
- Muscular differentiation time course
- Spermatogenesis cell types
- Reprogramming of fibroblasts to iPSCs
- Hematopoietic precursors and cell types
Other AS DBs: