Special

HsaINT0177869 @ hg19

Intron Retention

Gene
Description
unc-5 homolog B (C. elegans) [Source:HGNC Symbol;Acc:12568]
Coordinates
chr10:73044477-73045186:+
Coord C1 exon
chr10:73044477-73044620
Coord A exon
chr10:73044621-73045082
Coord C2 exon
chr10:73045083-73045186
Length
462 bp
Sequences
Splice sites
5' ss Seq
CCTGTACGC
5' ss Score
1.91
3' ss Seq
GACCCTCTCGCTTCTCCCAGACC
3' ss Score
9.52
Exon sequences
Seq C1 exon
GCCTGCGGGTGCGCGAGGTGCAGATCGAGGTGTCGCGGCAGCAGGTGGAGGAGCTCTTTGGGCTGGAGGATTACTGGTGCCAGTGCGTGGCCTGGAGCTCCGCGGGCACCACCAAGAGTCGCCGAGCCTACGTCCGCATCGCCT
Seq A exon
GTACGCCACCCTGACCCCCACCCTGTCCCTGCAGGAACCTTCCCCATCCCTGAGGATGCTGGAGAGGGAACTTCACATCTGTGGGGCCTCCTCCAGCATCCCTGGCTGAGGATGCCCACGGCAGAGACATCCCAGCACATGGATGCCAGCTCAGAGAGGGCTCCTAGACCCAGAACCTAGGCCTCTTTTCATCTACTTCTGTATAAAAGAAGCTGGCAGCTTCCTCCCCCATCCTGAGCCACTATATGCTTAGGATCCCAGAGTCAGGGAGGGAACCCTGTTCCCCCAAGTCTGCCTAGTGAGACCCCTCCTTTGGAGAAGAGGAAATTTCCCAGGCAAAGGCCAGGTGGGCCCATCAACAGTACCCTGGGTCTGCACTGCCACCCAGTGGCTACAGTGTAGCACATCAGGTTCTGATCCTGCCCGCACCTGACTGCCTTGGGACCCTCTCGCTTCTCCCAG
Seq C2 exon
ACCTGCGCAAGAACTTCGATCAGGAGCCTCTGGGCAAGGAGGTGCCCCTGGACCATGAGGTTCTCCTGCAGTGCCGCCCGCCGGAGGGGGTGCCTGTGGCCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000107731-UNC5B:NM_170744:3
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:
PF0767911=I-set=PU(34.1=88.6)


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:
CGAGGTGCAGATCGAGGTGTC
R:
GGCACTGCAGGAGAACCTCAT
Band lengths:
206-668
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains