Special

MmuINT0075761 @ mm9

Intron Retention

Gene
Description
hyaluronic acid binding protein 2 [Source:MGI Symbol;Acc:MGI:1196378]
Coordinates
chr19:56387359-56388720:+
Coord C1 exon
chr19:56387359-56387456
Coord A exon
chr19:56387457-56388464
Coord C2 exon
chr19:56388465-56388720
Length
1008 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGT
5' ss Score
10.1
3' ss Seq
TATCTTCATGTGCCCTATAGACA
3' ss Score
6.66
Exon sequences
Seq C1 exon
AAACCCAGATGGAGACCACAAACCCTGGTGTTTCGTCAAGGTGAACAGTGAGAAGGTGAAATGGGAATACTGTGATGTCACAGTCTGTCCAGTGCCTG
Seq A exon
GTGAGTCTGTGCTACCCACAAGGCCTGGGGAGGAAACGGGTGGTCTTGGGACAACCTGGTGGAAGCCCTGGTGACTGACCACTCCTACCCTTGACCCTTGCTTCACAAACAAACATATCACTCTTCCCAGGTTTCTGTAGCCCTCAGGACAATGAGCTAGCCTCGACACTTCTATCATCCCAGGTTAGATCTAAAACCTTTTTTCCTAACTCCAGGTCAGTACCTCAGTACCCTCAGCATCATACGCTGTGTGTGTCAGGTGGACAATGTCCATCACTGGCTGGGCCCTTGTGGCCTCTCAGGATGAGCTATGGTCTGAAGTCCAGCTTCTCGTTCTTTCTGACAGTCTTCATTAGCCCATCTCTCCACCCACATCTGAAAGAACGTGCCGATCTTTCTGACCAAAGGAATTCTCTCTCTGTTTCACACACGCAGCACTATTCTGTGGGTACCTCTCTGTAATGCTCGATCTCATATCTGCTTTTGTTTGTTTTTAACCATTCTTTGAGAACTGACCCAAGCATTCCTTTCTCTGACAAGCCCCCTTGAGCTCTTGAATTGGATGTTATATCTCCCTCTGTACAATCTCAAGGAACAGAACAAGCTTGCAGCCGTATAACCCATACACCCTTTGCTTGCCACAAATTTCTGGGAGAATCTCCTACCTCCCCTAATATACTAAAAAAAAAAAGCCTGAAAACATGCGTTAATGATGACATAATATGCATGAACATGATGGGTTTGTATATTTTTCGTATATGTTTGTACAACCTAGGAGTAATGCACTTCAAAATATGCAGATAAAAGCAACATCTTTCACACCAATTCTATGAAGTTGCTTTATATTACCTAAGTCATCCGACACGTCTCAGTCACTCACCAAACAACATATCGAAGGTGTGCCATCTCTTGGCTCTGAGCATTTGGTCAACTTGTGGTCAGAGTTATGACTCCAGCTATGTCCTCCAAAGGAACGGCTTGTGTGGTTTATCTTCATGTGCCCTATAG
Seq C2 exon
ACACCCCTAACCCAGTGGAAAGCCTTCTGGAGCCTGTGATGGAGCTGCCAGGGTTCGAGTCCTGCGGGAAGACGGAGGTAGCTGAACACGCAGTCAAGCGTATCTACGGGGGCTTTAAGAGCACAGCAGGCAAGCACCCGTGGCAGGTGTCCCTGCAGACCTCACTGCCGTTGACCACCTCCATGCCCCAAGGCCACTTCTGTGGGGGCGCCCTGATCCACCCCTGCTGGGTGCTCACTGCAGCCCACTGTACCGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000025075-Habp2:NM_146101:7
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.006 A=NA C2=0.013
Domain overlap (PFAM):

C1:
PF0005113=Kringle=PD(34.9=85.3)
A:
NA
C2:
PF0008921=Trypsin=PU(21.5=59.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGGAGACCACAAACCCTGGT
R:
GTACAGTGGGCTGCAGTGAG
Band lengths:
343-1351
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