Special

HsaINT0147219 @ hg38

Intron Retention

Gene
ENSG00000012171 | SEMA3B
Description
semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]
Coordinates
chr3:50274363-50274934:+
Coord C1 exon
chr3:50274363-50274582
Coord A exon
chr3:50274583-50274842
Coord C2 exon
chr3:50274843-50274934
Length
260 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGG
5' ss Score
7.2
3' ss Seq
ACCCCTTCTCATCCCTGCAGACG
3' ss Score
12.17
Exon sequences
Seq C1 exon
TGCCCCAGCAAGACCTTTGGCACCTTCAGTTCCACCAAGGACTTCCCAGACGATGTCATCCAGTTTGCGCGGAACCACCCCCTCATGTACAACTCTGTCCTGCCCACTGGGGGGCGCCCTCTTTTCCTACAAGTTGGAGCCAATTACACCTTCACTCAAATTGCCGCGGACCGGGTTGCAGCCGCTGACGGACACTATGACGTCCTCTTCATTGGCACAG
Seq A exon
GTCAGGGTCCCTCCACAGCGACCCCCAGGCTCCCAGCCAGGCCCTGTGGGCTGCTGATGGAAGCTCTCCCTGTTCAGTCCCATCTCCACATCCTTTCCTGGGCTGTGTCTCCACCCTGTGGATGCTGCCCAACCCACACTCTTCCAGTCCACACTCTTCACAACCCAAACATGCTGAGGGTAGACGCCTCAAAGGCGAGGAGACACTAGCCCCAGCTGTCCGGGAGCACCAATGGTCATTACCCCTTCTCATCCCTGCAG
Seq C2 exon
ACGTTGGCACGGTGCTGAAGGTGATCTCGGTCCCCAAGGGCAGTAGGCCCAGCGCAGAGGGGCTGCTCCTGGAGGAGCTGCACGTGTTTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000012171:ENST00000616701:11
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(47.4=100)
A:
NA
C2:
PF0140314=Sema=FE(19.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TTTGGCACCTTCAGTTCCACC
R:
CTCAAACACGTGCAGCTCCTC
Band lengths:
297-557
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