Special

MmuINT0075762 @ mm9

Intron Retention

Gene
Description
hyaluronic acid binding protein 2 [Source:MGI Symbol;Acc:MGI:1196378]
Coordinates
chr19:56388465-56389859:+
Coord C1 exon
chr19:56388465-56388720
Coord A exon
chr19:56388721-56389716
Coord C2 exon
chr19:56389717-56389859
Length
996 bp
Sequences
Splice sites
5' ss Seq
CGAGTAGGT
5' ss Score
5.76
3' ss Seq
CATCTTATTTTACTTTGTAGCAT
3' ss Score
7.96
Exon sequences
Seq C1 exon
ACACCCCTAACCCAGTGGAAAGCCTTCTGGAGCCTGTGATGGAGCTGCCAGGGTTCGAGTCCTGCGGGAAGACGGAGGTAGCTGAACACGCAGTCAAGCGTATCTACGGGGGCTTTAAGAGCACAGCAGGCAAGCACCCGTGGCAGGTGTCCCTGCAGACCTCACTGCCGTTGACCACCTCCATGCCCCAAGGCCACTTCTGTGGGGGCGCCCTGATCCACCCCTGCTGGGTGCTCACTGCAGCCCACTGTACCGA
Seq A exon
GTAGGTATCCATGGGGAAGGGAGAACAGATGACTGGGGTGCAAACAGCCTCTCTTTCCTCCAAGTGACACCTCAGAAGTTTTGGCAGGACTGGGGTTAAATGCCCAGAGGGGAAAGAACAGAGCCTTAATTGAGAGTGGATATAGCTACCATGGCTTACCACAGCTGTTCCATGAAGTCTACCATATGTAGCTAACTACCAAGAGAGGGCAGGGTTTGTGTGTTTTGTGAATTGTGTTATCCCTGATGCCTTTACTACAGAGGTCTTTCCATGTAGCAAGTATTTAGTATGTACGTTGAAGGAAAGATATATAGTTATGCCTTTTTTTTTAGGAGACTTGGGTTTTAGGAAAGTTTAATGTCTTAACTAAAGTCTCATGGAAAGAAGGCCAGTGAATGAGATTGAATTCAGCTCTGTCTTCTTCCTGAGCCTCTAGAGTCTACCCTGAATGGGCAAAATGGCCCATTATCATCAGTGAACCTCCAGGTCAGGCATTCTCATCTTCACCTCCAGTGTCTTCTGGGAACTGAGAAATCATCACCTCTTCCAGATTCTCTAAGTTCATGGTCAGGGCTGGTCTCATGAGCCCTGGCTTGAGAGGCAGCCTGCATAACTTCTGCTCTACTCTATCCTCTGGGATTCTAGTGTGGTTCCCCAAGAGAAGTTAGACACATGAACATTAGCACCTACTCACGAATGACAGCAGACTTGCTCAAGATTTCAATGGCTGACATGTAGCCAAGCCCAGAGGAAAAAAGAGATCTCCTGGGAAAAGTGAGTGTGTGATTGCACTCTCCATCTACTGATGAAGAAGTCCCATTGCATGGTCTTATCTGGAATCCAAACAGAGTTTTGTAAGGGAGCAAAGAACTGCAGATAAAGATACTGAAGCCGAAGGCCAGGCACTTTACCAAGGTCACATGGCTTCCTAGACTGCATAGCTCCTTCCTCTGTCATCTCAGGGCAATTTCCTGAGCATCTTATTTTACTTTGTAG
Seq C2 exon
CATAAACACCAAGCATCTAAAAGTTGTACTAGGGGATCAGGACCTGAAGAAGACAGAATCCCATGAACAGACCTTCAGGGTGGAAAAAATACTGAAGTACAGTCAGTATAATGAAAGAGATGAGATTCCCCACAATGACATTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000025075-Habp2:NM_146101:8
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.013 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=PU(21.5=59.3)
A:
NA
C2:
PF0008921=Trypsin=FE(20.3=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:
TTCGAGTCCTGCGGGAAGAC
R:
TGTCATTGTGGGGAATCTCATCT
Band lengths:
343-1339
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