Special

HsaINT0147301 @ hg38

Intron Retention

Gene
ENSG00000001617 | SEMA3F
Description
semaphorin 3F [Source:HGNC Symbol;Acc:HGNC:10728]
Coordinates
chr3:50182644-50183018:+
Coord C1 exon
chr3:50182644-50182783
Coord A exon
chr3:50182784-50182903
Coord C2 exon
chr3:50182904-50183018
Length
120 bp
Sequences
Splice sites
5' ss Seq
CTGGTATGC
5' ss Score
6.73
3' ss Seq
CCTCTTGCCCCACCCCCCAGAAC
3' ss Score
8.79
Exon sequences
Seq C1 exon
ACCCGTCGTTCATCCATGCTGAGCTCATTCCTGACAGTGCGGAGCGCAATGATGATAAGCTTTACTTCTTCTTCCGTGAGCGGTCGGCAGAGGCGCCGCAGAGCCCCGCGGTGTACGCCCGCATCGGGCGCATTTGCCTG
Seq A exon
GTATGCATTGGCAGAGCCACCAGGCTGCCCCTTCCACCAGTTCTGGCTTCATCAGCCCTGCTCCAGCCAGGGCTTGGGGTCAAGAGCTGATCTGACCCGGCCTCTTGCCCCACCCCCCAG
Seq C2 exon
AACGATGACGGTGGTCACTGTTGCCTGGTCAACAAGTGGAGCACATTCCTGAAGGCGCGGCTCGTCTGCTCTGTCCCGGGCGAGGATGGCATTGAGACTCACTTTGATGAGCTCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000001617:ENST00000002829:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.008 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=PD(19.2=95.2)
A:
NA
C2:
PF0140314=Sema=FE(11.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
ACCCGTCGTTCATCCATGCT
R:
GTGAGTCTCAATGCCATCCTCG
Band lengths:
242-362
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