Special

MmuINT0105100 @ mm9

Intron Retention

Gene
Description
expressed sequence N28178 [Source:MGI Symbol;Acc:MGI:2140712]
Coordinates
chr4:42947505-42950791:+
Coord C1 exon
chr4:42947505-42947690
Coord A exon
chr4:42947691-42950712
Coord C2 exon
chr4:42950713-42950791
Length
3022 bp
Sequences
Splice sites
5' ss Seq
TGTGTGAGT
5' ss Score
5.84
3' ss Seq
TCCGCTTCTACTTTCTTCAGGAC
3' ss Score
9.64
Exon sequences
Seq C1 exon
GTTGTCAACGACGAGATGTGTGACGTCTGTGAAGTCTGGACCGCTGAGAGCCTCTTCCCATGCAGAGTCTGCACCAGGGTTTTCCACGATGGTTGCCTGCGCCGCATGGGCTACCTCCAAGGGGACAGTGCAGTGGAGGTGACTGAGATGGCCCATACAGAGACAGGCTGGAGCTGTTACTACTGT
Seq A exon
GTGAGTCTGGACTGCAGGACAGGGGGAAAACTCGGTGTTCATCCCAGAGAAACTCTTAAAAGTGACTGTTTCTAAGTAGTGACCTAAGGGGCTTTTCTAATAGTGCATGCAAGGGTCCTGGAGCTAGAGGTGCAGTATATGGCACTTTTAAAACATGCCAGTAGCAAACAGGCCCAGTTGTAACACAGCAGACCTTGCCAAGTATGTTCCAGAGGGAGCAAGCCACCCTCGGTTAAGAATCATAAAAAGAACAGGCCTAACCTATCACTAGTCATTCTGCATGGGGCAGTGCTTTCTCTACAAGCCTGTGCCTGCCATTCCTTGTACTCATCTGAGAAACCAACCTGGCATCCTGAACAGCTCGCTTCCAGCAGAGGGAGATTCTGTTCCGGGAAAATACTTAGTCCCATGGTCCTCGCTTGACCTGCCGCCTGTTAGAAGCCTTTGTTCTTCGCCTCTGAAGTAATCATTATGTGAATTAAAGAGCAACACTGCATTGATTCAGAACTCTGAAAACCATATATAAATACCTTCCAACTTCTAATGGCAGAAAGAGTCTAAGGTTTCTGCTGAAAGCCGGATTCATAGCCATTTATCATCATGCCTGCGTGGAATCCAGGACTTCCCTGCCTGCTGTGCGGATGTCTTCCCTACTCTCTGGTTCGGTGTAAGGAGCAGCTGGCAACTGTCTTCTTCCACTGTCTGCAGAAAGCAGATAGGTGCTACTTTCTGACTCTCCATCTATGGCTAATCCACAAAATGAAGCCTACAAGTGACTTCCAGCTCCCGAAATACCTTCCCTGTAGAATATGCCACACCAGACTCTGTGCTACAGTCTTTCCCTCCACTTCTGCCCCAGTCTGTACACACACGCACACGCACGCACGCATGCACGCACGCACGCTTGCCAGTACGCTGCCAGCATGAGCCTGGGTCAATCTGTGTCCCTCTTCTGTCTCTCGGGCACTCTCTGCTTCCTTCCCAGCTCGCTAGGGGCCAGCTGCTGCCACCACCTCCACGGGCCTTTTGCACACCCTTCCTTCCAGTTCATCCCTTTCTTTTCCCTCCACTCACAATCACACTTCTTAAGAGCGTTTCACAGCCTCCTGACTTCTCTGCCCTGCAGTGTGACCTCGGCCGTCAGCACTTTGTTGAGTTGGCTTGTGTTGAGCCCACCGACAATCTTCTGTTTCTCAGGCATCTTCTTAGTCAGTCTTTTTCCTTGTTTCCTCCTCTTTCTCCTGGCAGTTAGGTATTTTCTAGAATTTATACAATATATGCAAGCTAGAGAAAGTGTTTCCAAATAACGAATCCCCGGATGCGTGTCTGACCAGTGCTAGCACCGCCCACTATGCCATGCCACAGCTATGCTATGCCATGCCCAGTCTTCGCTTGGTACCCAGTACTCCCAAGGGTCTTCCAGCCTTCTCTGACCTCTCCTCCGCACCCGTGGTTTGTTCCAGTTCTAGATGCTGTCTGTATTCCTCAGGATTCCATTGTCTTTCCCACTGTATTCGTTGTCTTCGAGTGACTTTGTCCTATAACCTACAATCAAATTATTAACGATGCCCGTATCGGTGCCCAGACTTAAATTTCCTGTCTCAGGGGCTTATCCATCTTGATGTCTCACCAGTACTTCATGCTCAGAATGTACCGAAATGAACTGATGTCCCTGCCTAAGCCTGCTCTTTCTCCATTCCTTTCTTCTGTGAGCAGTAGTATCTATCATTCCCCAGTTTCCCACCCCCCACTCTTCCGGTACCCTCCCTCATCCCCCACTGCCGGTACCCTCCCTCATCCTCCACTGCCTGTACCCTCCCTCATCCCCCACTGCCTGTACCCTCCCTCATCCCCCACTGCCGGTACCCTCCCTCATCCCCCACTGCCTGTACCCTCCCTCATCCCCCACTGCCTGTACCCTCCCTCATCCCCCACTGCCTGTACCCTCCCTCATCCCCCACTGCCGGTACATCAGCAGGTTCAATGACCTCTGACACCTCTCGCTTCTTCCCTCCCCTGTCCGCTGGGTTTAGCCACCTGCTTTTTCTTACCTGTGCCTCTGGAACAGCACCCAGCGGCGATCCATACCACCAGATTTTGCTCTTCTAATCTGACCATGACAGCTGCCCCTCTGTGCCTCCTCAATGTCCTTAGAGTAAAAGGTCTGAGTTACGGGGCCCCGTCAAGGCCATCTGAGGAGTGTCACAATTCTTCATTTCGAGTTCTCCCCGATTGCCTTCACACTCACATGCAGCAGCCACACAGTACCAAACATCCCAGTGCTGTGCACACTCATGTGCCCAGGACACGCCAGGCGCTCGGTGACAGAACCATAGGATTGCTTGTGAAACTCACGCCATGTCTGAGTCTGCTCCTGGCTGCTATTTTAGGAGGAAAGTTAACTAATCATTACAAAGAACCTTCAATAGTAATGCTAACAAAATAAGACCTCAATGCTGCTTTAGTAATTAAACTCCTATGACACCATAAAAATTGGTTTTGTTTAGGGACATTTCAAAACCCATTCTTGAGCCATTTAAAGTTGCACAACCCACTAGAAGCAGGGCTATTTGTTTTTTATAACTAAAATGTGCTTTAAGCCTGGCCACAAAGCCAGTGGACATAAAATAAACACATACTGAGCAGCTGATGGGTGGAGCTAGGACCTACAGCTGAGTACCTGTCTCTCTTTACACCCACAGCAGCTTTGGGGGTTGCTTCTGTGGCATCCCTAGGGCAGTTCACAGGCTAACTTGGAAGCAGGTATTGAATAAAGAGACTGGACTAGAGCCAGGATAGCTGGATTTTAGGGGGGTGGGGTTCATCCCTAGAGTCACTCAGCTCCAAGCAGATCTTCCCTCTGTCTGGCGCCCCAGTCTCCTTGACAGTGGCTGGGTGGTTGGGATCGTGGGTTTTACCTCCTCTCTGGTGGAGGTGCTGTTTCCGTCTCTCTTGATCCTTAGCGTTTCCCTTGTCACTGGCCTGTGTGGCCACTAGCTAACTCCGCTTCTACTTTCTTCAG
Seq C2 exon
GACAACCTTAACCTGCTGCTTACTGAGGAGGAGATGTATAGCCTTACTGAGACCTTTCAGCGGTGTAAAGTCATCCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000036062-N28178:NM_172690:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.015 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0013017=C1_1=WD(100=91.5),PF0062824=PHD=WD(100=68.1)
A:
NA
C2:
NO


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