Special

MmuINT0089627 @ mm9

Intron Retention

Gene
Description
laminin B1 [Source:MGI Symbol;Acc:MGI:96743]
Coordinates
chr12:31973068-31974286:+
Coord C1 exon
chr12:31973068-31973180
Coord A exon
chr12:31973181-31974206
Coord C2 exon
chr12:31974207-31974286
Length
1026 bp
Sequences
Splice sites
5' ss Seq
CTGGTAGGT
5' ss Score
8.37
3' ss Seq
ATTCATCTTCTGATCTGCAGCCG
3' ss Score
6.5
Exon sequences
Seq C1 exon
CATGTGCTTGCAATCCTCTGGGAACAATTCCTGGTGGGAATCCTTGTGATTCTGAGACTGGCTACTGCTACTGTAAGCGCCTGGTGACAGGACAGCGCTGTGACCAGTGCCTG
Seq A exon
GTAGGTAATCCTGATCTCTGCAGATGAGAAGGTAGTGACTCTGACATGTTTGTTTTGTTTTTGAGGTAGGGTCTCAGTATGTAGCCAAGGCTGGCTTTGAACCCACAATCCTCCCGACCCTGCCATCCAGGCCCTTGTATGTGCATACCCCATACCTGGCAGATGAGGAATGTCTTTCCCATTTTTATTTTTTAACCCATAATTTTTACTTTTACATTTTAATGTTAAGGAGAAAAGTCAAAATGAGGGATTCTAGTGAATCATTTGACAAACTGCAATGAATGCTGCTTATGAAGACAAGTGAACAAGTCTGTCTTTTTTTTAATGGCATTGCTAACAGCTGGGTAAGGACATGAGTTAGGACTTGTTAGCTTCGAACAGAAACAGGTCAACTTACACTGTGAAAAGTGTTTCAGAGAGGTGTCTCAGGAACTACTAAAAATGTAATATTCCTAAGCTAGTGACCTCACTTCTAAGGCTCCTCATGAGATCCTCAGAGAACTGGACAAAGGGGCATTCCTGATAGACTCATTGCACCCTTATTAATTATGGCAGGAAACTGTAATCGATAGTGGGGAAAATGGTTGCCTAAAGTTGGGGATTTCCATACAATGTGATATTCAGTTGTGGAAAATGACATTAATGCAAAGAAGTGTTTACTTCATTGCATTTACAAACAAAACAGACTCGAGGTGTGAATAACACTTTATGTAGGAAAAAATTTCATCAAGACAGACAAAAATTTGGAGGAAGCACACCAATAATACTGGCCGTAATTGTTCTTTCTGCCAGAGCCACTTGAATGAGGAAAACCGATCCCTGTCTGCTCACTCCGAGCCAGGCAGGCCTTTCTTTCATGTGGCACAAAGCTGAGTTTCTTTAGTAAGATTATTCCTACTCCGGGTCTGTTCCCTTGGTTGGAAGAAATACTTGGGCTAATCCAGGCAGGCTGCAGCTTGTTCTTTGCTGAGTCTCTTGTACAGCCAGAGGAGCCGTCCTTTACACGATTCATCTTCTGATCTGCAG
Seq C2 exon
CCGCAGCACTGGGGTTTAAGCAATGATTTGGATGGGTGTCGACCTTGTGACTGTGACCTTGGAGGGGCGCTGAACAATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000002900-Lamb1:NM_008482:11
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:
PF0005319=Laminin_EGF=PU(72.0=94.7)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(24.0=44.4),PF0005319=Laminin_EGF=PU(23.9=40.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGTGCTTGCAATCCTCTGGG
R:
TATTGTTCAGCGCCCCTCCAA
Band lengths:
191-1217
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