Special

MmuINT0078168 @ mm9

Intron Retention

Gene
Description
hemicentin 1 [Source:MGI Symbol;Acc:MGI:2685047]
Coordinates
chr1:152480740-152482333:-
Coord C1 exon
chr1:152482252-152482333
Coord A exon
chr1:152480877-152482251
Coord C2 exon
chr1:152480740-152480876
Length
1375 bp
Sequences
Splice sites
5' ss Seq
ACGGTAAAT
5' ss Score
7.76
3' ss Seq
TACTGTGTTCTCATGTTTAGTGC
3' ss Score
8.22
Exon sequences
Seq C1 exon
GTGGAGGATACAGGAAGATACACCTGCCTGGCATCCAGTCCTGCAGGGGATGATGATAAAGAATATTTAGTGAGAGTACACG
Seq A exon
GTAAATTTGGTGGCTTATGTTTGATCCACACACAACCCTAGTTAAAAACTGTACTAGAGAAAACTTGACATTTCACAACACATCATATGTTGATAAGTTGAAAAATACATACATATTTTACAAATTTTATTCTTAGTGTTAATAACATATGCGCTCTTTGGGATGTAGTTCATTGAAGTTTTGAGTTATTAGTCTCATTTTCACACAAAGAATTCAAATTTGATGTTTTAAAAATACCAGAACATAAATTACAATAATGATTAGAATAAAAACAATCCTTAGTCTTACCACATAACAATACAATGGTTTTTTTTATGTGAACATTAGATGGAAAAAAAAATGTGATCATAGTTGGGCATAGCAGCATATATCTGTAGTCCCAGCTTCTAGGGAAGTTGAGATAGGAAGATTGCCTAAGCTTAGAGTTTGCAACTGACTAGGGAATCAAGAAGATCCTTAATATCAAGAAAGTGACAATTCAGAACACAGAACTTAAGTTGCTTTATGTCTCACTTAATGGCGTGACAAACATTCTTATGTTAACAAATATATTCTATGGCATCATCTTTAAGATTGTATGTTGCCATATATCTTACTCCCTGTTTAGAGTTATTTAGGCAAATTAGGATATTCTGCCTTTTTATCTATATTAACAATATGTTAGCAACTCCCTTTATTTTTAAATTTTACTGAACTACACTTACTTGTTTATACATGCATGAATGTGCACATATATCCTTTTAAAGATATATGCCTTTTACTTGCCAGAAAGTTTGAATTAACTAGGCCCTTTCGAATAATATATATATATATATATATATATATATACTTAAACTGCTCTTCATGGAGAGAATTGTTTGAAAACTAAACAGATCTTTATCTAATTTTCAGAGCCTGACTGACTAGGCAATGCAGATTGTCTGGTATGAAGTTTCCCTGATATCTCTACTCAAAATTTAGCCTACCTAAGTAAACCCTAAAATATGATTTACTGAGAAATATATCTGTATTAATCAGGAAAAATGGACATAGTTCTTCGTACTGTGATGAGCAGTTCCTAATTCAGTAATTTTTTTGATAGTCAGGGAAAAGTATTGCCTATATGTCTCCATTTCCTTACCACCTGTCAAATGGTGGTGGTGATGTGGTTGTCGTATTATTTACATCATTGTTGGAAAGATTCCATTATTAAGCAACATGAAAGTGCTAAACAATAAAGATGCAATTTGTTAATAATCTAGACCATACATTGAATGGCAAACTGTTGAGGATCACGCCTCTTTTATCATACAATAAGCTTAACCCTTGCTGGATACTGATGGATCATTTACATCCCATTTATCAAACCCACTTGATACTGTGTTCTCATGTTTAG
Seq C2 exon
TGCCTCCTAATATTGCTGGCATGGATGAAGCCCAGGACTTCACTGTGTTAAGGAACAGGCAGGTGACACTGGAATGCAAATCCGATGCGGTGCCTCCACCTGTGATCATGTGGCTCAAAAACAGGGAGCAGTTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000066842-Hmcn1:NM_001024720:70
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.214 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0767911=I-set=PD(29.1=89.3)
A:
NA
C2:
PF0767911=I-set=PU(44.7=82.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGATACAGGAAGATACACCTGCC
R:
CTGTAACTGCTCCCTGTTTTTGA
Band lengths:
214-1589
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