Special

HsaEX6029689 @ hg38

Exon Skipping

Gene
ENSG00000084636 | COL16A1
Description
collagen type XVI alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2193]
Coordinates
chr1:31688467-31689085:-
Coord C1 exon
chr1:31689050-31689085
Coord A exon
chr1:31688861-31688971
Coord C2 exon
chr1:31688467-31688502
Length
111 bp
Sequences
Splice sites
3' ss Seq
CCTTCCTCTTCTTTCCCCAGGGG
3' ss Score
12.55
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
Exon sequences
Seq C1 exon
GGAGACCCTGGCATCCAAGGCATCAAAGGAGAGAAG
Seq A exon
GGGGAGCCCTGCTTGTCCTGCAGCTCGGTTGTAGGGGCCCAGCATCTTGTGTCCTCCACAGGGGCCAGTGGAGATGTGGGTTCCCCTGGCTTTGGTCTGCCTGGCCTTCCG
Seq C2 exon
GGTAGAGCTGGGGTTCCAGGGCTGAAAGGAGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000084636-'38-40,'38-38,39-40=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=0.730 C2=0.938
Domain overlap (PFAM):

C1:
NO
A:
PF0139113=Collagen=PU(25.4=43.2)
C2:
PF0139113=Collagen=FE(17.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains