Special

HsaINT0038824 @ hg19

Intron Retention

Gene
ENSG00000139219 | COL2A1
Description
collagen, type II, alpha 1 [Source:HGNC Symbol;Acc:2200]
Coordinates
chr12:48380618-48380959:-
Coord C1 exon
chr12:48380861-48380959
Coord A exon
chr12:48380672-48380860
Coord C2 exon
chr12:48380618-48380671
Length
189 bp
Sequences
Splice sites
5' ss Seq
ACGGTAAGA
5' ss Score
10.65
3' ss Seq
GACCTGCCTCTCTTTTCAAGGGT
3' ss Score
9.39
Exon sequences
Seq C1 exon
GGTGCTCCTGGCATTGCTGGTGCTCCTGGCTTCCCTGGGCCACGGGGCCCTCCTGGCCCTCAAGGTGCAACTGGTCCTCTGGGCCCGAAAGGTCAGACG
Seq A exon
GTAAGAGCCCAAAGTGACCCCCAAGTTCCACTGACATCTCTGGAGTCAAACCCCATCACCCCTCTTTCCCATGCTCTCCTGCCCTGGCCTCACAGCGGCCTCCATCCGAGGGCATCTTGAACAGGGGTTCTGGGGAGGGGCAGGCTCCCTGGAGAGAATCTGGTGTGAGGACCTGCCTCTCTTTTCAAG
Seq C2 exon
GGTGAACCTGGTATTGCTGGCTTCAAAGGTGAACAAGGCCCCAAGGGAGAACCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000139219-COL2A1:NM_001844:21
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=PD(16.1=42.4),PF0139113=Collagen=FE(38.1=100),PF0139113=Collagen=PU(37.5=81.8)
A:
NA
C2:
PF0139113=Collagen=FE(20.2=100),PF0139113=Collagen=FE(23.6=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:
CTCCTGGCATTGCTGGTGC
R:
TTCTCCCTTGGGGCCTTGTTC
Band lengths:
146-335
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