Special

HsaINT0147219 @ hg19

Intron Retention

Gene
ENSG00000012171 | SEMA3B
Description
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B [Source:HGNC Symbol;Acc:10724]
Coordinates
chr3:50311794-50312365:+
Coord C1 exon
chr3:50311794-50312013
Coord A exon
chr3:50312014-50312273
Coord C2 exon
chr3:50312274-50312365
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-SEMA3B:NM_001005914:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

NonCoding

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

C1:
NA
A:
NA
C2:
NA


Main Inclusion Isoform:
NA


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping 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