Special

HsaINT0146700 @ hg38

Intron Retention

Gene
ENSG00000148396 | SEC16A
Description
SEC16 homolog A, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:29006]
Coordinates
chr9:136446855-136447364:-
Coord C1 exon
chr9:136447227-136447364
Coord A exon
chr9:136446950-136447226
Coord C2 exon
chr9:136446855-136446949
Length
277 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGT
5' ss Score
10.28
3' ss Seq
CCTCGCTCTCTCATCCCCAGATG
3' ss Score
11.76
Exon sequences
Seq C1 exon
CAGGAACCAGAGCTCGCTACGTTGACGTCCTGAACCCAAGCGGGACCCAGCGGAGCGAGCCGGCTCTCGCTCCTGCGGACTTTGTCGCTCCACTCGCGCCACTCCCAATTCCTTCTAACTTGTTCGTGCCAACCCCAG
Seq A exon
GTAGGTAGCACGAGCACCAGCCCCTCCAGGTCAGCCCCCAGTCTCCTGACCTTTGATCCTCTTTCTATGAGTCTCTCCTAAATCTCCCGTTAAAAGAATGACCTGGCCAGCATGCAGAGAGCCTGGGGTTGGTTTGTGGTTTTTTTTTTGATTTGCCTGTTTCTGCATGAGTGTGCCGCGTGTGCAGTGTGAAACTCTCTTCCTCTCGGAGTGTCTTCAGTGAGACCCCAGGGACGTTCGGGACGGAATGATGGCCTCCTCGCTCTCTCATCCCCAG
Seq C2 exon
ATGCAGAAGAACCACAGCTTCCAGACGGGACTGGCAGGGAAGGGCCTGCAGCAGCTAGGGGCCTGGCCAATCCAGAGCCTGCCCCAGAGCCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148396:ENST00000371706:25
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.896 A=NA C2=1.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAACCAGAGCTCGCTACGTTG
R:
CTTGGGCTCTGGGGCAGG
Band lengths:
230-507
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development