HsaINT0038435 @ hg38
Intron Retention
Gene
ENSG00000164692 | COL1A2
Description
collagen type I alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2198]
Coordinates
chr7:94413083-94413743:+
Coord C1 exon
chr7:94413083-94413136
Coord A exon
chr7:94413137-94413689
Coord C2 exon
chr7:94413690-94413743
Length
553 bp
Sequences
Splice sites
5' ss Seq
CGGGTAGGT
5' ss Score
8.53
3' ss Seq
TTTCTGTTAAATATTTTTAGGGT
3' ss Score
8.44
Exon sequences
Seq C1 exon
GGTGATCCTGGCAAAAACGGTGATAAAGGTCATGCTGGTCTTGCTGGTGCTCGG
Seq A exon
GTAGGTGCTAACTTGTGTACAGATCTATTCACATAGCATTCATCTAAGAACCACACTTTTTTTTTTACACCATCTGATATCATTTTGTCACTTTCTTTTCAAGATGGCATCCCCAGGGGTCCTTTTACTATCATAAAATGCCTTTTTAAAAACCAAACTTATAAAACAGTGAGCAAAAACAAATCAGAATATACATTAGGTCAAAAATACAGAAGCACTTGGCTTTTATTTTATTCATTTTGTAATTAAAAGGGTATGAATATGTAGTAGCATTCTCTGGCCTTTATAAATTGCCTTGTGTCGCATACTTCGCTTGAGTCATATCAAAAGTTAGTAGGCAAACCCATAAATATATATACCTACTATGTACCCACACAAATTAAAAATTTAAAAAGTTAGTAGGCAGTATTTGGGCTTTCGTGGGAACCCACAATGAGTTTAATTCATGCTAAAATGACAAACTTGTTTTAAGGAAGTAATACCTGAGGCTTTGAGACATCTTAAACTACCTGGCTTGCAGCTAACCATCAGCCTTTCTGTTAAATATTTTTAG
Seq C2 exon
GGTGCTCCAGGTCCTGATGGAAACAATGGTGCTCAGGGACCTCCTGGACCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164692:ENST00000297268:26
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=FE(24.3=100)
A:
NA
C2:
PF0139113=Collagen=PD(12.9=50.0)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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