Special

HsaINT0147289 @ hg38

Intron Retention

Gene
ENSG00000001617 | SEMA3F
Description
semaphorin 3F [Source:HGNC Symbol;Acc:HGNC:10728]
Coordinates
chr3:50185443-50185707:+
Coord C1 exon
chr3:50185443-50185531
Coord A exon
chr3:50185532-50185665
Coord C2 exon
chr3:50185666-50185707
Length
134 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGT
5' ss Score
8.23
3' ss Seq
TGATCTTTATCTTTTTCTAGGAT
3' ss Score
10.82
Exon sequences
Seq C1 exon
ACCGCGGGACAGTGCAGAAGGTCATTGTGCTGCCCAAGGATGACCAGGAGTTGGAGGAGCTCATGCTGGAGGAGGTGGAGGTCTTCAAG
Seq A exon
GTGGGTGTGACACCACCCAGTCCTGACCTCCCCACCTTTACCCTCCCCCCAGTCCCAGCCTCTGACCTGAGACCTCTAGGTCAGGGCAGGGAGGGGGTCCCTGGCATCCCAAGCTGATCTTTATCTTTTTCTAG
Seq C2 exon
GATCCAGCACCCGTCAAGACCATGACCATCTCTTCTAAGAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000001617:ENST00000002829:14
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.033 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(6.1=100)
A:
NA
C2:
PF0140314=Sema=FE(2.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGGACAGTGCAGAAGGTCATT
R:
TCTTAGAAGAGATGGTCATGGTCT
Band lengths:
124-258
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