Special

HsaINT0147304 @ hg38

Intron Retention

Gene
ENSG00000010319 | SEMA3G
Description
semaphorin 3G [Source:HGNC Symbol;Acc:HGNC:30400]
Coordinates
chr3:52439680-52440098:-
Coord C1 exon
chr3:52439867-52440098
Coord A exon
chr3:52439772-52439866
Coord C2 exon
chr3:52439680-52439771
Length
95 bp
Sequences
Splice sites
5' ss Seq
CTGGTAGGA
5' ss Score
6.77
3' ss Seq
CCCCTCCTCCCTGGCCCCAGACT
3' ss Score
8.38
Exon sequences
Seq C1 exon
TGCCCCAGCAAGATGACCGCACAGCCAGGACGGCCTTTTGGCAGCACCAAGGACTACCCAGATGAGGTGCTGCAGTTTGCCCGAGCCCACCCCCTCATGTTCTGGCCTGTGCGGCCTCGACATGGCCGCCCTGTCCTTGTCAAGACCCACCTGGCCCAGCAGCTACACCAGATCGTGGTGGACCGCGTGGAGGCAGAGGATGGGACCTACGATGTCATTTTCCTGGGGACTG
Seq A exon
GTAGGACAGCTGAGCCAGGGTGGCCAGGCTGGAGAGGGGTGTGGGGTCTCTGGCTGTCCCCTCCTGTCCCGCTGACCCCTCCTCCCTGGCCCCAG
Seq C2 exon
ACTCAGGGTCTGTGCTCAAAGTCATCGCTCTCCAGGCAGGGGGCTCAGCTGAACCTGAGGAAGTGGTTCTGGAGGAGCTCCAGGTGTTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000010319:ENST00000231721:11
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.103 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0140314=Sema=FE(17.3=100)
A:
NA
C2:
PF0140314=Sema=FE(6.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGTCCTTGTCAAGACCCACCT
R:
ACCACTTCCTCAGGTTCAGCT
Band lengths:
168-263
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