MmuINT0139967 @ mm9
Intron Retention
Gene
ENSMUSG00000020877 | Scrn2
Description
secernin 2 [Source:MGI Symbol;Acc:MGI:1343092]
Coordinates
chr11:96892194-96893602:+
Coord C1 exon
chr11:96892194-96892375
Coord A exon
chr11:96892376-96893402
Coord C2 exon
chr11:96893403-96893602
Length
1027 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGAG
5' ss Score
7.1
3' ss Seq
GTACTCTGATTTTCTATCAGGCT
3' ss Score
7.5
Exon sequences
Seq C1 exon
TGTACCTATATCGAGGTGGAACAGGTGGGGAAGACACACGCTGTGATTCTGAGCCGCCCCTCTTGGCTGTGGGGAGCTGAGATGGGGGCCAACGAGCTTGGTGTCTGCATTGGAAACGAAGCAGTGTGGACCAAAGAGCCTGTGGGGCAGGGGGAAGCCCTGCTGGGTATGGACCTGCTCAG
Seq A exon
GTAGAGAGCTGCTCTTCAGTGCCCCACTTCCTCCCACCTAGCCTGAGTCTATTGGGCTTGTCTCTGTTGGCCTTGCCCTTGAGGCCTTTCTAAGGCGGCTGCAGTCTTATATCTTCCTAGTCTGATAAAGGACCTCCCTTGGCCTAGAGTGCTTTAATTTTTTTTTCAGTACTTTTTGTTTTGAGACAGGGTTTCTCTGTGTAGCCTTGGCTGTCCAGGAATTTGCTCTGTAGACCAGGATGGCCTTGAATTCACAGAGATCCTCCTGCCTGTGTGCCACCACACATAGTTCAGTACAACTTTTGTTTGTTTGTTTTTTGGTTTTTCAAGACAGGGTTTCTCTGTGTAGCCCTGGCTGTCCTGGAACTCACTCTGTAGACCAGGCTGGCCTCGAACTCAGAAATCCACCTGCCTCTGTCTCCCAGGTGCTAGGATTAAAGGCATGCACCACCACTGCCCAGTACTACTTTTGTTAATTGAAATATTACATAGTTGCGGTTTATAAAAACTGGTAAATGTGAGGCAGCCCCGCCTGAGGAGAGGTTCAGGCGGTTTTTCCTTGGAGAGAGTGTTCCAGACCTTTCCATGGAATTCACAGTCCTTAGCTTGGCAACTATATGGTTTATTATTGTTTTTTCATGTTTGTTTGTTTTTGTTTTATTTTATGTTTTGAGACAGGGTCTCACTGCATAACCCTGACTGGCTTAGAATTCACTATGTAGACCAGGCTAGCCTCAAACTCACAGAGATCTGCCCGCCTCCCAAGTGCTGGGGTTGAAAGTGTGTACCACTACTCCAGCTGATTTTTCACTTTGCTTTGGTATTTTTGTTTGTTTGTTTTAAGAGATCATGTAGTATGTAGCTGAGTCCAGAGATGAACTTCTGATCTCCCTGCCTCCACTCCGGAGGAATCACAGGCCTGGCCTGCATGATTGTTTAATACCATCATGGCTGCTGGGTTTGCTGTGCTACGTGGGCTTTTCATCAAACCCGTGTGGACCGCTTCTGTACTCTGATTTTCTATCAG
Seq C2 exon
GCTGGCTTTGGAACGGAGCAGCACTGCCCAGGAGGCTGTTCACGTGATTGCAGGCTTGCTGGACCGCTATGGGCAGGGAGGCAGCTGCCGGGAGGATCCAGAGCCGTTCTGCTATCACAACACCTTTTTACTGGCTGATCGGACAGAGGCGTGGGTGCTGGAGACAGCTGGGAGCCTGTGGGCTGCTCAGCGGATCCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000020877-Scrn2:NM_146027:3
Average complexity
IR-S
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:
PF0357710=Peptidase_C69=PU(21.0=60.7)
A:
NA
C2:
PF0357710=Peptidase_C69=PD(50.4=96.9)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Cow
(bosTau6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GAACAGGTGGGGAAGACACAC
R:
ACAGGCTCCCAGCTGTCTC
Band lengths:
343-1370
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: