Special

HsaINT0147226 @ hg38

Intron Retention

Gene
ENSG00000012171 | SEMA3B
Description
semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]
Coordinates
chr3:50270127-50270495:+
Coord C1 exon
chr3:50270127-50270284
Coord A exon
chr3:50270285-50270432
Coord C2 exon
chr3:50270433-50270495
Length
148 bp
Sequences
Splice sites
5' ss Seq
AAGGTGCCA
5' ss Score
3.41
3' ss Seq
CTCCCCCAACCTCCCGATAGCTG
3' ss Score
8
Exon sequences
Seq C1 exon
AGCTCCAGGCCTGGCATGGTCTCCAGACTTTCAGCCTGGAGCGAACCTGCTGCTACCAGGCCTTGCTGGTGGATGAGGAGCGTGGACGCCTGTTTGTGGGTGCCGAGAACCATGTGGCCTCCCTCAACCTGGACAACATCAGCAAGCGGGCCAAGAAG
Seq A exon
GTGCCAGGGACTCCCAACCCCAGCACTCCCCAGGGAAGGAGCCCTGGGACCCCACTCCAGCCTGGAGAGACCCAGAGGAATGGCTCCCTGAGGTAGAGAATATCCCAAGTTCCTGACCTGTGTCCCCTCTCCCCCAACCTCCCGATAG
Seq C2 exon
CTGGCCTGGCCGGCCCCTGTGGAATGGCGAGAGGAGTGCAACTGGGCAGGGAAGGACATTGGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000012171:ENST00000616701:2
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=PU(21.2=64.2)
A:
NA
C2:
PF0140314=Sema=FE(12.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CCTGGCATGGTCTCCAGACTT
R:
CAATGTCCTTCCCTGCCCAG
Band lengths:
210-358
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