Special

HsaINT0177866 @ hg19

Intron Retention

Gene
Description
unc-5 homolog B (C. elegans) [Source:HGNC Symbol;Acc:12568]
Coordinates
chr10:73056335-73057847:+
Coord C1 exon
chr10:73056335-73056499
Coord A exon
chr10:73056500-73057665
Coord C2 exon
chr10:73057666-73057847
Length
1166 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGG
5' ss Score
8.41
3' ss Seq
CTTGGCCCCCACCCTTGCAGACA
3' ss Score
9.29
Exon sequences
Seq C1 exon
GAGATCCCCTTCTATCACATTTGGAGTGGCAGCCAGAAGGCCCTCCACTGCACTTTCACCCTGGAGAGGCACAGCTTGGCCTCCACAGAGCTCACCTGCAAGATCTGCGTGCGGCAAGTGGAAGGGGAGGGCCAGATATTCCAGCTGCATACCACTCTGGCAGAG
Seq A exon
GTGAGGGAAGTCGGGGCCACATATTCCAGCTGCACACCACACTGGCGGAGGTGAGGGAAGGGTGGGGCAGATATTCCAGCTGCACACCACGCTGGCGGAGGTGAGGGAAGGGTGGGGCAGATATTCCAGCTGCACACCACGCTGGCGGAGGTGAGGGAAGGGTGGGGCAGATATTCCAGCTGCACACCACGCTGGCGGAGGTGAGGGAAGGGCGGCCAGATATTCCGGCTGCACACCACTCTGGTGGAGGTGAGGGAAGGGCGGCCAGATATTCCGGCTGCACAGCACTGTGGCATAGGTGAGGGAAGGGCCGCCAGATATTCCAGCTGCACACCACGCTGGTGGAGGTGAGGGCCAGAGGATACCTCTAGGGTTTGGGGCTGGGCTGCAGCACACAGAACCCTGTAGTTCCCTCTCACCTCCCAAGTCTGAGCGGGTATCTGGTCATGTTTTTCTAACAAGTGTCATTTATTGATTGAGTGCCATTCACATGCTTGGCATATACCAAAAAACTTACATGATCTCACAAGCACCGGGAGATGCATGACAGATATCATCCCCACCTGGGAGGTGAGAAAGTAGGTTTTAGGAAGGGCAAGGATTTGCACACAGTACACCAGTGGCAAGACTGGATTCGAACCCAGGTTGATGCAAGGACCAGGCCTGTGGTTCTCAACCGTTAAAAATCCGGATTGAGATTTAAAAACCCAGGCCACCCAGGGTGACAACACTAGATCCTCCTCTTGGGGCATTGTAAAGAGCACTGGATACAGGTCTGGACCCAGGTCTGCCACTAACTTGGCATGTGGCCATGAGCAAGCCACTCCCCTTTTCTAGACTTCACTTTCCACCTGTACAAGAGGGTGCATGTGGATTAGACTGTGGCTGGGCCTCCTTGGGGCTTCCTAACCATGAGGCTGCATCTGCATTTGCCTGGGGCCTTAGGTAAGCATGGTGCACCCCCTGAGGCCTGAAGGGTGGCCATGCAGGCCTTGCCCTTGGGAACCGACCCTTCAAGGGAGAAGCCCCTGCCTGAACAGTGGGAGTCTGTCCAGAGGAGGTGGGAGTGACTCAAGGCTCAATGAGCTCACAGTCCAAGGGGAGGGAGGCTGGAGGGCAGATGCCCAGCACTGTGCCCCTCTCACTCTTGGCCCCCACCCTTGCAG
Seq C2 exon
ACACCTGCTGGCTCCCTGGACACTCTCTGCTCTGCCCCTGGCAGCACTGTCACCACCCAGCTGGGACCTTATGCCTTCAAGATCCCACTGTCCATCCGCCAGAAGATATGCAACAGCCTAGATGCCCCCAACTCACGGGGCAATGACTGGCGGATGTTAGCACAGAAGCTCTCTATGGACCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000107731-UNC5B:NM_170744:15
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
NO
A:
NA
C2:
PF0053117=Death=PU(34.2=44.3)


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:
CCCCTTCTATCACATTTGGAGTGG
R:
CGGTCCATAGAGAGCTTCTGTG
Band lengths:
342-1508
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains