Special

HsaINT0147342 @ hg19

Intron Retention

Gene
ENSG00000185033 | SEMA4B
Description
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B [Source:HGNC Symbol;Acc:10730]
Coordinates
chr15:90763025-90764325:+
Coord C1 exon
chr15:90763025-90763123
Coord A exon
chr15:90763124-90764213
Coord C2 exon
chr15:90764214-90764325
Length
1090 bp
Sequences
Splice sites
5' ss Seq
ATCGTGAGT
5' ss Score
8.88
3' ss Seq
ATGTGTCCACCCTCCTGCAGAAC
3' ss Score
10.81
Exon sequences
Seq C1 exon
CGCGACTGTCAAAACTACATCAAGATCCTCCTGCCGCTCAGCGGCAGTCACCTGTTCACCTGTGGCACAGCAGCCTTCAGCCCCATGTGTACCTACATC
Seq A exon
GTGAGTGACCTGTCCTCAGCCCTGAGGCTGACCTGGGAACTGCCCCTCTTTCTGCCCCAGGGATCCTGTTCTGTAGCATAGACCCCTGAGGAAAGGCAGGGCCCAGAGGGAGGTTTCTAGGTACCACTGGCCTCCAAGAGCCCTGAGGTCCCACACCCTGGCACAAAGCGCAGCCCTGACAGCCATGTCTCCCTGTGCGGGGAGGCGGGGGCACATGCGGTCACTTACCCATGAAGATCCTGTGCCACCCAGGCCTTGCTGCCCTCTTCTGCTTCTTCCAGCATCTCTCCCTCTCCTTTGCTTGATTCTCTTGTCTTATCTTGTACACCCCCTCCTCAGCACACACCCCTAGCAGAGGGTGGCATTTGATGCTGTGGGTTGGAGCCCAGCTTTGGGGTCAGACACACCTGGGTTTGAATCACATTGCTGCCCCTTCCAGGCTCACATCATTTTATTTCTTTTTTCTTTTTCTTTTCTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCTGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACGCCTGGCTAATTTTTTCTATTTTTCGGTAGAGAGGGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCAGGCTCACATCATTTTCTAAGCCTCACCTCCTCCGCCAGGTGGGTCTGATAATGTGTCCCGCGTCGGGTCACTGTGAGGCAGTGTGGCACTGTGTCTGGGTGAGGCCTCTCCTGAGGCCGACTGTCCAGGTTCAAACCCTTCGGCACCGTGTCCTGGCTGAGGAGGACGGCGTCCCTGACACCTGACCCCTTCTGTCCCACACACCTCACCTGCCTGCAGAGTTGCCTTCTCCTGCACGCCTCTCTCTTTCTCACCAAGCCTGCTCCTCATTCCCTGGAGTGCCCCTGAGCCCATGTGTCCACCCTCCTGCAG
Seq C2 exon
AACATGGAGAACTTCACCCTGGCAAGGGACGAGAAGGGGAATGTCCTCCTGGAAGATGGCAAGGGCCGTTGTCCCTTCGACCCGAATTTCAAGTCCACTGCCCTGGTGGTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185033-SEMA4B:NM_020210:5
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=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(32.0=100)
A:
NA
C2:
PF0140314=Sema=FE(15.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CGCGACTGTCAAAACTACATCA
R:
ACCAGGGCAGTGGACTTGAAA
Band lengths:
206-1296
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