Special

HsaINT0039825 @ hg38

Intron Retention

Gene
ENSG00000092758 | COL9A3
Description
collagen type IX alpha 3 chain [Source:HGNC Symbol;Acc:HGNC:2219]
Coordinates
chr20:62830517-62832189:+
Coord C1 exon
chr20:62830517-62830588
Coord A exon
chr20:62830589-62832153
Coord C2 exon
chr20:62832154-62832189
Length
1565 bp
Sequences
Splice sites
5' ss Seq
CGGGTAAGT
5' ss Score
10.75
3' ss Seq
AGCCTTCTCTCCACATCCAGGGT
3' ss Score
7.61
Exon sequences
Seq C1 exon
GGCCAGAAGGGCAGCATGGGAGACCCCGGCCTTCCAGGCCCCCAGGGCCTCCGAGGTGACGTGGGCGACCGG
Seq A exon
GTAAGTGGCCCTCTCAGCAGGAAGCTCCCCTGCACCCCCTCTACCCATGTACCACAGTCCCCCACCCCCATGACAGTCCCCCAACCCCCACCACAGTCCCCCAACCCCTACCACAGTCCCCCAACCCCCACCACAGTCCCCACCCCCTACCACAGTCCCCCAACCCCCACCACAGTCCCCCACCCCCTACCACAATCCCCCACCCCCCACCACAGTCCCCTGGGACGCAGACAGGGAGAGGCCCTTGCAGCTCCCAGTGGGAAATCTGGCCATGGGCAGTGTCTCCCTGCGTGGCGGAGGCAGTGGCATCAGGGCCCCGACTGTGGCGCCTTTGGCCCCTCTGACCTTCCACGTGGTGTTCCTTGTGGGTGGGAGGCTGCGGGAGCCTGGGCCGCTCTGCCTCCTGCCCTGCGTAGACGCCTGGCGGGACCTGCACACGGTCAGTGTTCATTCCTCGAGATTGGCGTGGAGGCTGAGGCTCAAGAGCCACGCCTGCTCCCGCCTAGCGGGTGTCTGCGGAGGCGCGGTTGACAGAGGATCACGTTGCTATAAAATAGGTTTGAACACCATGTCCCAAGTGACTGTAACGGTCACAGCTTCTACCTCGTCAAGACTTTTTCCTGCTGGTCTTGCAGCAGCTGCAGCATTAGCTCCTTGGGGGTCCGGGCAGAAGCGGGGCACGGCCTACCCAGGGCCCCAGCTCACTGGAAGGAGCCTGTGGGTCTGGTCTGGGCCCCAGCCATGCTCCACCAGGTCCTTGGGGACCTCGTGTGCCTGCTGTGGCCACCTCTGCTGGGCAGACAGACCCCTTTTTAGATGTCAATCCCGAGAAGCCTCCAGGACACGGCTGCAGATGCCCCGTCATTCCAGGGTGATGGTCATTCCAGGGTGATGGCCGGGGCTGTGGACACCACCACCCCATGGGGGATAGCGGGCTGTTTATTGGCCTCCAGGCAGGACATTCCAGAGGTGGGGGCCATGCCAGCAACCTCAGGGCCTCCGAGAGATGGCAGGGCTGGCACCCGCCCTGCGGGCACTGCGCCTGTCCCAGGTGTGGGTGGGGCCTGGTGGCTGAATTTCCCTTTCACTTTAAACTCACGGGAAAGTCTCCTGCTTTTCTGCCCTTTGGGCCAGTTCTCACTTATGTGGCCATGTGAGCAAATGGACATTTTTTAAAGGGATTCATAGCAACTCCCAGACATGTCCTCATTTCACAATGCCGGGGGAAGGTGATTAGATGAGCTTTTGCATCTTTGACTCTACTGTGACGGAATTATCCTGCAATTGTGCAGAAACACCCGCACGAATTCACGGGTGTTACAAACAGTGCAAACCTAACGGGACTTCACTACCCACAAGGGGAGGCTGGACAGAGCCATCGGGCCCAGAGGCTGTGAACGTGAGCTTGGCCTTTGGGCCTGTGTCTGGGAGCCGGTGTTCACAGAAGCCCTTTGTGCAGCACAGATGGAGATGTGGGGAGGTGTTTACCATTCCTGGGCCCAGGGCAGGCTCACTTTAGGGATTCCTGCCATTCCTCTAATCCAGAGCCTTCTCTCCACATCCAG
Seq C2 exon
GGTCCGGGAGGTGCCGCAGGCCCTAAGGGAGACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000092758:ENST00000343916:24
Average complexity
IR
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=PD(25.6=83.3),PF0139113=Collagen=FE(31.1=100)
A:
NA
C2:
PF0139113=Collagen=FE(14.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


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

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