Special

HsaINT0039821 @ hg19

Intron Retention

Gene
ENSG00000092758 | COL9A3
Description
collagen, type IX, alpha 3 [Source:HGNC Symbol;Acc:2219]
Coordinates
chr20:61460807-61461033:+
Coord C1 exon
chr20:61460807-61460851
Coord A exon
chr20:61460852-61460979
Coord C2 exon
chr20:61460980-61461033
Length
128 bp
Sequences
Splice sites
5' ss Seq
CGGGTATGT
5' ss Score
8.79
3' ss Seq
CAGCTCTCCTTCCTCTACAGGGC
3' ss Score
9.45
Exon sequences
Seq C1 exon
GGCCTCCCTGGACGAGCGGGGTCCAAAGGCGAGAAGGGAGAACGG
Seq A exon
GTATGTGGCTGCAGCCGCTTTCTCTCTGGGAGGGGAGGCGAGGGGCCGGGAGGCAAGGGGCTGGGGGGCCAGCGACCTGGCCCCAGTGCAGGTGTAGGCAGGCACTCACAGCTCTCCTTCCTCTACAG
Seq C2 exon
GGCAGAGCTGGGGAGCTGGGTGAGGCCGGCCCCTCTGGAGAGCCAGGCGTCCCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000092758-COL9A3:NM_001853:20
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0139113=Collagen=FE(15.6=100),PF0139113=Collagen=PU(6.0=33.3)
A:
NA
C2:
PF0139113=Collagen=FE(18.9=100),PF0139113=Collagen=FE(20.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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
  • Pre-implantation embryo development