Special

HsaINT0146687 @ hg38

Intron Retention

Gene
ENSG00000148396 | SEC16A
Description
SEC16 homolog A, endoplasmic reticulum export factor [Source:HGNC Symbol;Acc:HGNC:29006]
Coordinates
chr9:136459444-136459874:-
Coord C1 exon
chr9:136459757-136459874
Coord A exon
chr9:136459556-136459756
Coord C2 exon
chr9:136459444-136459555
Length
201 bp
Sequences
Splice sites
5' ss Seq
TGGGTAGGT
5' ss Score
6.86
3' ss Seq
GTCGTGTCGTCTCTCCGCAGCTT
3' ss Score
9.98
Exon sequences
Seq C1 exon
TGCTGTGGAGACGAGAAATGGGGAGATTGGAGGCCGCACCTCGCCATGGTCTTGTCCAACTTGAACAACAACATGGACGTCGAGTCCAGGACGATGGCTACCATGGGCGACACTCTGG
Seq A exon
GTAGGTCAGGGGTGGAGATGGGCATTGGGTGTCGCGGATGGAGCGCCGAAGGCCCGGTTGTCTGTGGCGTTGGCAGAAATCACCAGAACCCGGCCTTCTCGGTCCGGCTGGCGTCTCTGGTGCCTTCTGTGCGCGTCCTTGACTTCTGCAAGCGCTCCCGGTCGCTGAGCCCCCGCCGTGTGTCGTGTCGTCTCTCCGCAG
Seq C2 exon
CTTCAAGGGGCCTCTTGGATGCGGCCCACTTCTGCTACCTCATGGCCCAGGCGGGATTTGGTGTTTACACGAAGAAAACTACAAAGCTTGTCTTAATCGGATCCAATCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148396:ENST00000371706:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

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

C1:
PF129312=Sec16_C=FE(14.8=100)
A:
NA
C2:
PF129312=Sec16_C=FE(14.1=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:
GCTGTGGAGACGAGAAATGGG
R:
TGTGATTGGATCCGATTAAGACA
Band lengths:
228-429
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