Special

MmuINT0093486 @ mm9

Intron Retention

Gene
Description
leucine rich repeat and sterile alpha motif containing 1 [Source:MGI Symbol;Acc:MGI:2684789]
Coordinates
chr2:32810701-32812072:-
Coord C1 exon
chr2:32811995-32812072
Coord A exon
chr2:32810770-32811994
Coord C2 exon
chr2:32810701-32810769
Length
1225 bp
Sequences
Splice sites
5' ss Seq
AAGGTACTG
5' ss Score
8.56
3' ss Seq
CTGACATGTTTGTTCTGTAGGTT
3' ss Score
10.09
Exon sequences
Seq C1 exon
GTGTTGATTGTCCATACAAACCACCTCACCTCCCTGCTTCCCAAGTCCTGCAGCCTCTTGAGCCTTGTCACCATCAAG
Seq A exon
GTACTGGGCGTCCTCCAGGCATCGGGGACTGGGGTCCAGGTGGCAGCTGAGCCTCTACACCCTCCTAGTGTTCTCTGTTAAAGTTTATAGTTGTGTGTGGCTGGTAAAGAGAGGGCAACTTGACTCCTCAGTGACCAGCATGGCCTCCCTCCTCCCTGTGGATCCCTCCTGGACATGGTAGATCATAGTATAGTTACAGGTCAGCCACAGATTATTCTGTATGGAGGTGAAGCTGGTAGGGTGGGTCCTTTACCCTAGGAGTAAAGACTGAAAATGTACACTCTCCTCCACGCTAGCTCCCACAGGTGGGGTTGGGGTAGTTTTGGCTCCATGGCGGTTCTTTTGTTAAGCAGTAGTCTCACTATGCAGTCAGTCCTAGCTGGCCTAGAACTGGCTATGCTCAAGCCTTTACCATGCTGATTACCCGCTCTGCCTCTGAGTCCCACCCCAGGCCATGCATAATTTTTATAGTCAGTAAAATGAGAATACTGAAGCCAGACATGGTAGCGAATATCTACAATCCTGAGACTGACAAAGAGGCTGAGGCAAGAGAATTGATCTAGCCTGGGCTACATCTTAAGAGCCTTGCTCTAAACCTTAAAAGAAGACTATGAGCTGGTGAGCTGCTGGAGTTGGGAGTGCTGGCATATCCCTTTAGTCCCAGCAGAGGCGGGCAGATCTCTGAGTTCAAGGCCAGCCAGGACTACATACCGAGACCTTGCTTCAAAAAAGGGGCAGGGCCTGGAGAGATGGCTCAGAGGTTAAGAGCACTGTCAGCTCTTCCAGAGGTCCTGAGTTCAATTCCCAGCAACCACATGGTGGCTCACAGTCATCTGTAATGGGATCTGATGCCTTTTTCTGGTGTGTCTGTCTGAAGACAGTGACAGTGTACTCACATAAAATAAATGAATAAGTCTTTTAAAAAAAAAACACAGATATGGTGATGCACACCTTTAATCCCAGCACTCAGAGGCTGGTGGGTCTCGGAGTTTGAGACCAGCCTGATCTACAGTGTGAGTTGTGAGTTCCAGGATAGCCAGTGCTATGTAGAGAGCCCATCTCAAAACACTACAAATAATAATATATAAAAGATCTGTGAGATAGAATGCGGACCGGTGGGCAGGAGGAAGGGGCACCACCAAACTGCCAGGGTACGAGGTGGCCTTATCACCTGTCAGCTGCTCTGGAGTCTGGGATTTGGGGGCCTGACATGTTTGTTCTGTAG
Seq C2 exon
GTTCTGGATCTCCATGAGAACCAGCTGACAGCCCTTCCTGATGACATGGGGCAGCTGACAGTCCTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000026792-Lrsam1:NM_199302:5
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:
PF138551=LRR_8=PD(46.2=92.3),PF127992=LRR_4=PU(6.5=11.5)
A:
NA
C2:
PF127992=LRR_4=FE(48.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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