Special

HsaINT0147517 @ hg38

Intron Retention

Gene
ENSG00000137872 | SEMA6D
Description
semaphorin 6D [Source:HGNC Symbol;Acc:HGNC:16770]
Coordinates
chr15:47760978-47761220:+
Coord C1 exon
chr15:47760978-47761038
Coord A exon
chr15:47761039-47761157
Coord C2 exon
chr15:47761158-47761220
Length
119 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGC
5' ss Score
9.6
3' ss Seq
GTTTTGCTTGATTAATACAGAAA
3' ss Score
3.13
Exon sequences
Seq C1 exon
GGATCAAGTTTATACAGTAAACTTAAATGAAATGCCCAAAACAGAAGTAATACCCAACAAG
Seq A exon
GTGAGCAACTGTAGTTGGCAAATTTATTTACCTTCCCTCTGAACCTGATTAATTTTCCCACTGCCTCCCCAAAAATGTTCGCAGTTAAAAACTGCTTTGGTTTTGCTTGATTAATACAG
Seq C2 exon
AAACTGACATGGCGATCAAGACAACAGGATCGAGAAAACTGTGCTATGAAAGGCAAGCATAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137872:ENST00000558014:7
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=0.238
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(12.3=100)
A:
NA
C2:
PF0140314=Sema=FE(12.3=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:
ACAGTAAACTTAAATGAAATGCCCA
R:
TGCTTGCCTTTCATAGCACAGT
Band lengths:
107-226
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