Special

MmuINT0162672 @ mm10

Intron Retention

Gene
ENSMUSG00000037129 | Tmprss13
Description
transmembrane protease, serine 13 [Source:MGI Symbol;Acc:MGI:2682935]
Coordinates
chr9:45337046-45338418:+
Coord C1 exon
chr9:45337046-45337089
Coord A exon
chr9:45337090-45338255
Coord C2 exon
chr9:45338256-45338418
Length
1166 bp
Sequences
Splice sites
5' ss Seq
CCCGTAAGC
5' ss Score
4.37
3' ss Seq
TCCTCTCCATTTTCTCCCAGACT
3' ss Score
8.38
Exon sequences
Seq C1 exon
GTCGCAATGTCCTTCCCGGCGGTATGTCTCCCTCCAGTGTTCCC
Seq A exon
GTAAGCTGTTTCTCTTTTTGGAGTGTGGTCTATGGGGGTGGGATGAGATGCTGTCTAAGGAGCTCAGTCCTGTTACCTGTCATTCCCAGGGAGTCATATGAGTCTCCTAAACCTTTGCTGGAAACTGAGTGAGGACAGCAGGTGTGGGCTAGCTGATAGTTTTGTGTCAACATTCACTTGAATGCTTGCCCATGGAGGATACTGCATCAGCGTCTGTACAGACAGGGCAGGAGTTACTGATTCAGAGCCCTGCAAGGCAATAGCCATTACTGGGCACTGTGCCTTGCCTAAGATCAGAAACCAGGCAGGTGGGGAGCTGACACCTGACCTTGGAGTTGGCCCCTAAGCCCTAACTGTGAGTGACCCCACAAGGTTTATGTTCTTGGTGGTGAAGCCAGGGTGCAGGCTGTCCCACTGTTGTGGCTGTAGTGCCCACTGCTCAGATGGTGTGCCACCCTCTCTCCTCTGCAAGCAGAAAAGCCCCATACCTGAGCTCACTCAGCAGGCTGCCCCTCCCCGCCCTGGGCTTGACTCATTCGAGACTTGTTCCCTGTGCAAGCCCAGCTATGCATCATAGGAAATCTATTTATTTCTCCTTCATTTTGAAATGAGAGACTGCCAGACTAGTGCTTACCAGTTCAGGGTTGTGATAGCATCTTTTGCTTTTCTGAGCCCTTGATGACAGTCCTGGGATTCACCCTCTTAACCAAGCCAAACTCCACGCTGAAGCACTGGACATGGAGTGAGCATTTGCCAGATGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGGAAGGAAGGAAGAAAAAGAGAGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGGAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGGGAACAAGGTGGAAGCTGCCTGGGGTCAGACTTCACTAGACACCTCCAGAAGGCTAAGACCACCTTGTACTACTTCTGCTTGGACAGGGAATAGGTGTGCCACATTAGACTCTTTGGACAAAGGGTGACCTTCAGTTGCCTGCCCGGAGCTCGAGAAGAGCAGGAGAGGCTCTAAAAGAAGCATATGACATGTTCTGTCCTCTCCATTTTCTCCCAG
Seq C2 exon
ACTGTGGTTTGAGAGCTATGACCGGGCGGATCGTGGGAGGGGCTCTGACCTCGGAGAGCAAGTGGCCCTGGCAAGTTAGCCTGCACTTCGGCACCACCCACATCTGTGGGGGCACACTCATCGATGCCCAGTGGGTGCTCACCGCTGCCCACTGTTTCTTTGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000037129:ENSMUST00000034597:7
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:
PF154941=SRCR_2=FE(16.5=100)
A:
NA
C2:
PF154941=SRCR_2=PD(5.5=9.1),PF0008921=Trypsin=PU(19.2=80.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTCGCAATGTCCTTCCCGG
R:
ACAAAGAAACAGTGGGCAGCG
Band lengths:
207-1373
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • Ribosome-engaged transcriptomes of neuronal types
  • Neural differentiation time course
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types