Special

HsaINT0038839 @ hg38

Intron Retention

Gene
ENSG00000139219 | COL2A1
Description
collagen type II alpha 1 chain [Source:HGNC Symbol;Acc:HGNC:2200]
Coordinates
chr12:47981776-47982160:-
Coord C1 exon
chr12:47982107-47982160
Coord A exon
chr12:47981830-47982106
Coord C2 exon
chr12:47981776-47981829
Length
277 bp
Sequences
Splice sites
5' ss Seq
CGAGTAAGT
5' ss Score
10.15
3' ss Seq
TCTACCTGCTCTCCCCGCAGGGC
3' ss Score
13.53
Exon sequences
Seq C1 exon
GGTGACGTTGGTGAGAAAGGCCCTGAGGGAGCCCCTGGAAAGGATGGTGGACGA
Seq A exon
GTAAGTGAATGCGGGCTGCTGGACTGCTGGGCATTAGGATCCTAGCCCTGCACCCAGGAGAGCAGGAGAGAGGGCTGGGCAGTCTGCCACTGGGGTCCCTGGTCCTGTCTCTGTCGGGGCTGGGCAACTGCAGGGACTTCTCTGTTAAAATGGGGCCAGAGGGTAAGTGGGAGCTCTGGAGGCGGTGGGAGCACGCACCAAGGTTGGCTTGGTGCCGGGCCGCACGTGCTCGGCTGGCTCAGCCTGCCTCCCTCACCTCTACCTGCTCTCCCCGCAG
Seq C2 exon
GGCCTGACAGGTCCCATTGGCCCCCCTGGCCCAGCTGGTGCTAATGGCGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000139219:ENST00000380518:35
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(0.1=0.0),PF0139113=Collagen=FE(23.9=100)
A:
NA
C2:
PF0139113=Collagen=FE(23.9=100),PF0139113=Collagen=PU(15.9=61.1)


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