Special

HsaINT0147231 @ hg38

Intron Retention

Gene
ENSG00000012171 | SEMA3B
Description
semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]
Coordinates
chr3:50273298-50273646:+
Coord C1 exon
chr3:50273298-50273443
Coord A exon
chr3:50273444-50273534
Coord C2 exon
chr3:50273535-50273646
Length
91 bp
Sequences
Splice sites
5' ss Seq
CGGGTGAGG
5' ss Score
8.48
3' ss Seq
CCCTTTGATCGTCCCGGCAGAAC
3' ss Score
9.8
Exon sequences
Seq C1 exon
AGCCCAAGTTTGTCAAGGTATTTTGGATCCCGGAGAGCGAGAACCCAGACGACGACAAAATCTACTTCTTCTTTCGTGAGACGGCGGTAGAGGCGGCGCCGGCACTGGGACGCCTGTCCGTGTCCCGCGTTGGCCAGATCTGCCGG
Seq A exon
GTGAGGAGTCCCTGGGCCACACCCGGCGACCCTGCCCCTACCCCTTTGCCTGCCCTGGTCTCGCCCTCATCCCCTTTGATCGTCCCGGCAG
Seq C2 exon
AACGACGTGGGCGGCCAGCGCAGCCTGGTCAACAAGTGGACGACGTTCCTGAAGGCGCGGCTGGTGTGCTCGGTGCCCGGCGTCGAGGGCGACACCCACTTCGATCAGCTCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000012171:ENST00000616701:7
Average complexity
IR
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:
PF0140314=Sema=FE(10.9=100)
A:
NA
C2:
PF0140314=Sema=FE(8.4=100)


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:
ATTTTGGATCCCGGAGAGCGA
R:
AACGTCGTCCACTTGTTGACC
Band lengths:
174-265
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development