Special

HsaINT0147513 @ hg38

Intron Retention

Gene
ENSG00000137872 | SEMA6D
Description
semaphorin 6D [Source:HGNC Symbol;Acc:HGNC:16770]
Coordinates
chr15:47765869-47766182:+
Coord C1 exon
chr15:47765869-47766009
Coord A exon
chr15:47766010-47766104
Coord C2 exon
chr15:47766105-47766182
Length
95 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGC
5' ss Score
7.31
3' ss Seq
TTCTGTTTGGTTTTACACAGGTC
3' ss Score
9.24
Exon sequences
Seq C1 exon
GTGCAGTGCTGAGAATGAGGAAGACAAAAAGGTCATCTCATTACAGTTGGATAAAGATCACCACGCTTTATATGTGGCGTTCTCTAGCTGCATTATCCGCATCCCCCTCAGTCGCTGTGAGCGTTATGGATCATGTAAAAA
Seq A exon
GTAAGCTCGTGTTTCTTTACTTACCCTGGGTCTTGCAGTATCGAAACCTTTGTTGATGAGAAAATCCAAGTTACATTCTGTTTGGTTTTACACAG
Seq C2 exon
GTCTTGTATTGCATCTCGTGACCCGTATTGTGGCTGGTTAAGCCAGGGATCCTGTGGTAGAGTGACCCCAGGGATGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137872:ENST00000558014:17
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=0.006
Domain overlap (PFAM):

C1:
PF0140314=Sema=PD(1.6=14.6),PF0143720=PSI=PU(15.0=18.8)
A:
NA
C2:
PF0143720=PSI=FE(43.3=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:
GTGCAGTGCTGAGAATGAGGA
R:
TAACCAGCCACAATACGGGTC
Band lengths:
181-276
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