Special

HsaINT0147482 @ hg19

Intron Retention

Gene
ENSG00000167680 | SEMA6B
Description
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6B [Source:HGNC Symbol;Acc:10739]
Coordinates
chr19:4550811-4552651:-
Coord C1 exon
chr19:4552434-4552651
Coord A exon
chr19:4550943-4552433
Coord C2 exon
chr19:4550811-4550942
Length
1491 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGC
5' ss Score
7.16
3' ss Seq
CTTTCATCCCAACCCCTCAGCAT
3' ss Score
5.94
Exon sequences
Seq C1 exon
GTGGTGGTGTCCCGCGTGGCCCGAGTGTGCAAGAACGACGTGGGAGGCTCCCCCCGCGTGCTGGAGAAGCAGTGGACGTCCTTCCTGAAGGCGCGGCTCAACTGCTCTGTACCCGGAGACTCCCATTTCTACTTCAACGTGCTGCAGGCTGTCACGGGCGTGGTCAGCCTCGGGGGCCGGCCCGTGGTCCTGGCCGTTTTTTCCACGCCCAGCAACAG
Seq A exon
GTCAGCGCCCACCAATGGGAGCAAACTGGGAGCATTTGGTGGGCATGGGTAGAGAGGGCCTGTATTCACTCCTCAGGTATGCCCTGGGTGCTAGGTTGGGCACCACTGGATTAGACCTCTGAGAGGCCTCGGCCCCAGGCTGGGGTGGGACAAGCTGACACTGACCCTCTAAGTCCCTTTGGTCAGAACTGGGCCAAAGATATCCTCATCCTCTGCCTTTGGGGAGAGGAGCAGGGAGGGCTTCCTGGAGGAGGGGACATTGGAGCTGGACTTTGGGTGTGAGATGGAGGAAGAGGGAAGGGTGTTCAAAGTTGGAGAAACAGCATGTGCAAAGGTCCTGAGGCTTCAGTGAGTTCAGTATACTTAAGTAATCGTGAGAGAGTCTGTGTGGGAAGGGAACTAGGGGAGAATGCACAACAGGAAAGCAGGGAACTGGTAGGATGGATCAGGCAAGGCTTTGTGGGCTGCAGGCAGAAACTTGGACTTTTTCCCTGAGAGCACTGGGGAGCCATGGAAGAGTGAAGAGCAAGAGGGATGAGATCAGGTTTGCATTTTTTGTTTGTTTGTTTGTTTGTTTGGTTTGGTTTTTTTTTTGAGACAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACCACAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCGTGCGCCACCACACCCAGCTTATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATTTTGGTCAGGCTGGACTCAAACTCCTGACCTCGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTCAGCCACCGCACCCGGCCAAGGTTTGCATTTTTAAAAAGCCTGCTTGTGGACTGGGCACGGTGGCTTCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGAGGGCAGATCACTTGAGGTCAGGAGTTCGAAACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGGGCACCTGTAATTCCAGCTACTCGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGTAGGTTACAGTGACCTGAGATCACGTCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCGGTCTCCAAAAAAAAAAAAAAAAGCCTGCTGGGGAGTGGGCTCTAACAGTGACACTGGGCAGGCAGGACATCCAGTTAAACAGGGATGGGGGCCTGGACAGGGGTGGCCTCGTAGACCCTGAACTGTGGCCCAATCTGAGATGTTATTCAGGAGGAGTGGCTGCATTCGACAGATGCGGGAGGGACAGGGGACATCTCTGGCCTAGGAAGACTGAAGATTCACTGGCTCCTGCAGACAGAGGCTCCTGCACGCACTTGTCCGAGATGGGGCCTCCCACCGGGCTCACCAAACTCTTTCATCCCAACCCCTCAG
Seq C2 exon
CATCCCTGGCTCGGCTGTCTGCGCCTTTGACCTGACACAGGTGGCAGCTGTGTTTGAAGGCCGCTTCCGAGAGCAGAAGTCCCCCGAGTCCATCTGGACGCCGGTGCCGGAGGATCAGGTGCCTCGACCCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167680-SEMA6B:NM_032108:9
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.289
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(17.1=100)
A:
NA
C2:
PF0140314=Sema=FE(10.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGGCCCGAGTGTGCAAG
R:
GGGGTCGAGGCACCTGAT
Band lengths:
334-1825
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