Special

HsaINT0147272 @ hg38

Intron Retention

Gene
ENSG00000170381 | SEMA3E
Description
semaphorin 3E [Source:HGNC Symbol;Acc:HGNC:10727]
Coordinates
chr7:83392555-83394338:-
Coord C1 exon
chr7:83394297-83394338
Coord A exon
chr7:83392722-83394296
Coord C2 exon
chr7:83392555-83392721
Length
1575 bp
Sequences
Splice sites
5' ss Seq
CGGGTAAGT
5' ss Score
10.75
3' ss Seq
CCTCTTTCTGATTTCTGTAGCAA
3' ss Score
7.92
Exon sequences
Seq C1 exon
GATCCAGTTCCTATTATTTCTATGGAGATTTCTTCAAAGCGG
Seq A exon
GTAAGTTCTGTGTGTGTGTGTGTGTAGGTGTGTGTGTTCTATATGTGAGCTAAGGTAAGGTCAAAGGATATGAGAACATTAGTACATGTGCTTAAATATGAACTTATTACAGTTTTATTTTTCTTTTATTACTTTATTTTATTGTAGTAAGAACTTTTAACATGTGATCTACCCTGTTAACAAAATATTAAGCATACAATACATTTTTAATGGTTATAGGTACAGTGTTATACTGCAGACCTCTAAACCTTATTAATCTTGTTTGACTGAAACTTTATGTCCATTGATTGATTCTGACAAAAGTTTATCATGATTTACATTTGATACTTGTTTTCATTTTCTATCTCTATAGAAAGGAAGATGAGAGTAGTTTTACTTCTACAATCATGATAACACTTTATTCCCTGGTTATTTTTCACTAATGTTTTTCAAAAACAATGGTAACAATGATAATCCAATAGTGTGCAAGAACAATGATAATCCAATAGTGTGCAAGGAAACACACCTCCTTTCCACTTCACTGAAATCAGTTTGGTGTAAACTTCTTTAGAAACAGTTGTTGCATATATTGCCCCAAATTTATTTATAAATAATCCTTCATGTTCAGGCAAAAGGAAAGATATTATATTAAATGTTCAGCCACTTGTTCTGTAGATAGATAGATAGATATACACATCACTCTTCTAAATGTTATATGTCAATATTTAAAAGACTATTTGCTTTCCAAATCTCTTATTAGTTTTTGCTATAGATTTGTTTTCTGTTTTTGAGATAAAGTCTCACTGTGTCACCCAGGCTGGAGTTCAGTGGTGCAATTACAGCTCACTGCAGACTCAACCTCCCCAGGGTCAGGTCATCCTTCTGTGTCAGCCTCGTGAGTAGCTGAGACCACAGGCACATATTACCAGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAATTTACCTGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTACAGGCATAAACCCAGCCGTTTCTATAGATCTTTAAAGGAAGATCCACAGTGTTGGGTAATGCAAGATAATGAACACAGCTTCTTGAGTTCTTGTCAAGTTCAGTGTAGCAATTTTGGTACTCCTGCATTTATGTCTATGAATGTTTCTCAAATATTAGAGAAATGAAAGTATAAATATTATCTATATTGAACAACTGCTATAATTTTTTTTTTTTTTTTTTGAGATGGAGTTTCTCTCTTGTCGCCCAGGTTCCACCTCCACATCCTAGGTTCAAGCAATTCTCCTGCCTTAACCTCCAGAGTAGCTGAGATTACAGGCATCCGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGTGCAGGCTGGTCTCAAACTCCTGAAACTGCTAATTTAAGTGAATTAAATTTAAGTGAATTTTTTCTGAGGTGATTGTGTATAAATGTGAAAACTAGGTGTAATAGCTCAGTGAAAGTTTTGTCCATTTCTGCTAGTGACCTCTTTCTGATTTCTGTAG
Seq C2 exon
CAACAGCTGTATATTGGATCTGCTTCTGCTGTGGCTCAAGTCAGATTCCATCACTGTGACATGTATGGAAGTGCTTGTGCTGACTGCTGCCTGGCTCGAGACCCTTACTGTGCCTGGGATGGCATATCCTGCTCCCGGTATTACCCAACAGGCACACATGCAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170381:ENST00000307792:13
Average complexity
IR
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(2.9=100)
A:
NA
C2:
PF0143720=PSI=PU(65.5=67.9)


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:
TCTATGGAGATTTCTTCAAAGCGG
R:
GCATGTGTGCCTGTTGGGTAA
Band lengths:
185-1760
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