Special

MmuINT0075760 @ mm9

Intron Retention

Gene
Description
hyaluronic acid binding protein 2 [Source:MGI Symbol;Acc:MGI:1196378]
Coordinates
chr19:56386161-56387456:+
Coord C1 exon
chr19:56386161-56386332
Coord A exon
chr19:56386333-56387358
Coord C2 exon
chr19:56387359-56387456
Length
1026 bp
Sequences
Splice sites
5' ss Seq
CAGGTACGA
5' ss Score
10.03
3' ss Seq
ACTTAAATTTTGTGTTTTAGAAA
3' ss Score
9.68
Exon sequences
Seq C1 exon
GTCCGGACGACTGTTATGTCGGTGATGGCTACTCTTACCGAGGCAAAGTGAGTAAGACAGTCAACCAGAACCCATGCCTTTACTGGAACTCCCACCTCCTCTTGCAGGAGACTTATAACATGTTTATGGAGGATGCAGAGACCCACGGGATCGCAGAGCACAACTTCTGCAG
Seq A exon
GTACGAACTACTGCCGCCTGTAGGTCCCATCTTGGTTGCTTGACTTTGAAACCGATTGCAAGTCAGCAGCCTTCTTTCTGAACAGGGAAGCATCCTACTCGGGATAACATAACAATAAAAACTCCCCTAGTCTCGGGGCCTCGTGCACATCGAAGTTCATTTCTTACTAACTACACGTGTCGTGTGGGTGGGACGGTGATGGGGGTGGGGTGGGTGCAGCACCAGAGTATTGCAGATACCCAGCAAGGGTAAAAAGAGAACAATGAGGCAAAAAAAAAAAAAAAAAGGCAACCAAAACCCAAGAAATGACACCTTACCTTCCACATGAATTCTGGGATTCTGTGGCAGAAATAGTCACATGGAGCCACTTGCCATCAAGAGAGAGGCTGAGGGACAAATGGATTAGACTTCCCGAGTCATCTGTCTCCAGACAACTTCTGGGTTCCTAGCTCTACCTTTAGTCTGACCAAGGTCGATGACTTGCGAGATTTGTGTACGGAGAGTGAGGGTGTTTCGCTTGTCTTTGCACTGGCCCCACACGCAATGGTGTCTTCTTTGCACACAGCACCCTACCTCTGTTTTCTTAATGCTCACTCGGAGATGCCTTCTTGTGGCGCTATCTTCATAGAGAAACTCTTTGACTAGTTCCCAAAGGATTCTCATGCCTGGGACTTGGAGGTTGGGGCCAGCTTTCACCGTGTCTGTCTGTCTGTCTATAATACTTCCTAAACACATTGAGTGGGGATCTTCAGTAGGAACCCCTCTTCTCCTATGTTTCCTGTCTCCCATGGTCCAGCACACTGGTTGGAAACTACTTTCTGGTCCTCAGGATTCTCCTCCTGACAGTAACATTTTGCCCAACATCTGTGAGCATGCTTGTATGCCAAGGTTTGCTAACCTGTTGGAGGATTCAGTGAAGAATGGTTCCCAGATGTGTGGGGATCAGGAATCCTCTGACTCAGGGTGCTTCCATGATATGAATGCCTCTGAGCCTTGATGGTCAGTCACTTAAATTTTGTGTTTTAG
Seq C2 exon
AAACCCAGATGGAGACCACAAACCCTGGTGTTTCGTCAAGGTGAACAGTGAGAAGGTGAAATGGGAATACTGTGATGTCACAGTCTGTCCAGTGCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000025075-Habp2:NM_146101:6
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.001 A=NA C2=0.006
Domain overlap (PFAM):

C1:
PF0005113=Kringle=PU(63.9=91.4)
A:
NA
C2:
PF0005113=Kringle=PD(34.9=85.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTCCGGACGACTGTTATGTC
R:
GCACTGGACAGACTGTGACAT
Band lengths:
267-1293
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