Special

HsaINT0146687 @ hg19

Intron Retention

Gene
ENSG00000148396 | SEC16A
Description
SEC16 homolog A (S. cerevisiae) [Source:HGNC Symbol;Acc:29006]
Coordinates
chr9:139353896-139354326:-
Coord C1 exon
chr9:139354209-139354326
Coord A exon
chr9:139354008-139354208
Coord C2 exon
chr9:139353896-139354007
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-SEC16A:NM_014866:15
Average complexity
IR-S
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(14.9=100)
A:
NA
C2:
PF129312=Sec16_C=FE(14.2=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