Special

HsaINT0147335 @ hg38

Intron Retention

Gene
ENSG00000185033 | SEMA4B
Description
semaphorin 4B [Source:HGNC Symbol;Acc:HGNC:10730]
Coordinates
chr15:90224968-90225397:+
Coord C1 exon
chr15:90224968-90225178
Coord A exon
chr15:90225179-90225281
Coord C2 exon
chr15:90225282-90225397
Length
103 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGT
5' ss Score
10.65
3' ss Seq
GAGTCCTGTCCACACCCCAGGTG
3' ss Score
4.01
Exon sequences
Seq C1 exon
TGCATCACCAACAGTGCCCGGGAAAGGAAGATCAACTCATCCCTGCAGCTCCCAGACCGCGTGCTGAACTTCCTCAAGGACCACTTCCTGATGGACGGGCAGGTCCGAAGCCGCATGCTGCTGCTGCAGCCCCAGGCTCGCTACCAGCGCGTGGCTGTACACCGCGTCCCTGGCCTGCACCACACCTACGATGTCCTCTTCCTGGGCACTG
Seq A exon
GTAAGTGTCTGCAGCCCAGCAGGCTCAGGGGAAGGGGTGCACGTGGCTGGTGGGTCATGGGCAGTGGGCTCCACCCAGGGCCTGAGTCCTGTCCACACCCCAG
Seq C2 exon
GTGACGGCCGGCTCCACAAGGCAGTGAGCGTGGGCCCCCGGGTGCACATCATTGAGGAGCTGCAGATCTTCTCATCGGGACAGCCCGTGCAGAATCTGCTCCTGGACACCCACAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185033:ENST00000411539:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.058 A=NA C2=0.021
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(16.0=100)
A:
NA
C2:
PF0140314=Sema=PD(52.0=78.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCCCGGGAAAGGAAGATCAAC
R:
AGCTCCTCAATGATGTGCACC
Band lengths:
257-360
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