Special

HsaINT0147224 @ hg38

Intron Retention

Gene
ENSG00000012171 | SEMA3B
Description
semaphorin 3B [Source:HGNC Symbol;Acc:HGNC:10724]
Coordinates
chr3:50275705-50277179:+
Coord C1 exon
chr3:50275705-50275844
Coord A exon
chr3:50275845-50276301
Coord C2 exon
chr3:50276302-50277179
Length
457 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
ACGCTGCCCTCTGCCCGCAGGTG
3' ss Score
13.34
Exon sequences
Seq C1 exon
ACTCGTCTCGTCCCGCGCTGCTGGAACACAAGGTGTTCGGCGTGGAGGGCAGCAGCGCCTTTCTGGAGTGTGAGCCCCGCTCGCTGCAGGCGCGCGTGGAGTGGACTTTCCAGCGCGCAGGGGTGACAGCCCACACCCAG
Seq A exon
GTGAGCCTTACTCCGCCCTCCCCGCCAGGCTCCTGTCCCACCCCCTGCATCCAGGAGAGGCCCCGCCCTACCCAACGAAGCCCCGTCCAACCAGACCCACTCCCCGCCCTGTCCAGTTTGGTCCCTCACCTGCACTCCACAAGCTGCTGAGGCCCCATTGCGTCCAACGGGGCTCCCGACCCGCCTCCCCTGAATCAAGGAGAAGACCCGCCCTCGACCCTCCCATTAAGGTCCCTGACCACCCCCCACCAAGTTCATGTAAACCCCGCCTCTTTCGGATTCTCCCTTGAAGACCACCAGCTCCCAAACACTCAGCCTTAAAATGTGCGCCTGCGGGCACCCCTTTCCCGCTCCACCTCGGCTCCCAATGACTCTTTGCTTCTTCCGTCGCGTGCTAGGGCCCGGAAGCCCTGTTCCCGGCCCGACACCCCCGCCTCACGCTGCCCTCTGCCCGCAG
Seq C2 exon
GTGCTGGCAGAGGAGCGCACCGAGCGCACCGCCCGGGGACTACTGCTGCGCAGGCTGCGGCGCCGGGACTCGGGCGTGTACTTGTGCGCCGCCGTCGAGCAGGGCTTTACGCAACCGCTGCGTCGCCTGTCGCTGCACGTGTTGAGTGCTACGCAGGCCGAACGACTGGCGCGGGCCGAGGAGGCTGCGCCCGCCGCGCCGCCGGGCCCCAAACTCTGGTACCGGGACTTTCTGCAGCTGGTGGAGCCGGGCGGAGGTGGCAGCGCGAACTCCCTGCGCATGTGCCGCCCGCAGCCTGCGCTGCAGTCACTGCCCCTGGAGTCGCGGAGAAAGGGCCGTAACCGGAGGACCCACGCCCCTGAGCCTCGCGCTGAGCGGGGGCCGCGCAGCGCAACGCACTGGTGACCAGACTGTCCCCACGCCGGGAACCAAGCAGGAGACGACAGGCGAGAGAGGAGCCAGACAGACCCTGAAAAGAAGGACGGGTTGGGGCCGGGCACATTGGGGGTCACCGGCCGATGGAGACACCAACCGACAGGCCCTGGCTGAGGGCAGCTGCGCGGGCTTATTTATTAACAGGATAACCCTTGAATGTAGCAGCCCCGGGAGGGCGGCACAGGTCGGGCGCAGGATTCAGCCGGAGGGAAGGGACGGGGAAGCCGAGCTCCAGAGCAACGACCAGGGCCGAGGAGGTGCCTGGAGTGCCCACCCTGGGAGACAGACCCCACCTCCTTGGGTAGTGAGCAGTGAGCAGAAAGCTGTGAACAGGCTGGGCTGCTGGAGGTGGGGCGAGGCAGGCCGACTGTACTAAAGTAACGCAATAAACGCATTATCAGCCAAAGCTGGAATGGCCCCAGCAGAAAACCCCAGTCCTCGGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000012171:ENST00000616701:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.470
Domain overlap (PFAM):

C1:
PF0143720=PSI=PD(14.1=19.1),PF0768612=V-set=FE(45.5=100)
A:
NA
C2:
PF0768612=V-set=PD(45.5=34.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAAGGTGTTCGGCGTGGAG
R:
CTCCACCAGCTGCAGAAAGTC
Band lengths:
358-815
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