HsaINT0039299 @ hg38
Intron Retention
Gene
ENSG00000204262 | COL5A2
Description
collagen type V alpha 2 chain [Source:HGNC Symbol;Acc:HGNC:2210]
Coordinates
chr2:189068226-189068884:-
Coord C1 exon
chr2:189068786-189068884
Coord A exon
chr2:189068271-189068785
Coord C2 exon
chr2:189068226-189068270
Length
515 bp
Sequences
Splice sites
5' ss Seq
CCTGTAAGT
5' ss Score
7.52
3' ss Seq
ACTTTTAATGTACCTTTTAGGGT
3' ss Score
8.91
Exon sequences
Seq C1 exon
GGAGAAGCAGGTCCTACAGGGGCGCGAGGCCCTGAAGGTCCTCAGGGGCAGAGAGGTGAAACTGGGCCCCCAGGTCCAGTTGGCTCTCCAGGTCTTCCT
Seq A exon
GTAAGTTTCTAGCATATTTAAGAACCAGCCCAGAAAGCTGGACATTTCTTGTAACATCAGAACAAATTCAACCTATTTTTTTAATTGATACATAATATTTGTACATATTTAGGGGGTACCTGTAATGTTCTGTTATATGCCTAAGATGTGTAATAATCAAGTCAGGGTATTTAAGATATCCATCCCATTGAGCATATATCACTTCTATGTGTTGGGAACATTTTAAGTCCTCTTTTTCTAGCTATTTTGAAATATAAAATTTAATATATTCTCTGAATTCTGAATGAGTGCTTACAACTGTGAAAAAATATATTTCCCTTGTCAACTCTGTAAGTTTTACCTATTTTATGTAAAGGAGAAGTAGTCAAAAAAGTAATTTTTATGATATAATGGTGGTTGATTTTTAAAAAATGCTTCTACTTCCTTTTTGAAGATGGCTGGACATCTGTATACTAGCACATTTGTATCTATATATTGCTTAATATTTCATTACATACTTTTAATGTACCTTTTAG
Seq C2 exon
GGTGCAATAGGAACTGATGGTACTCCTGGTGCCAAAGGCCCAACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204262:ENST00000374866:19
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:
NO
A:
NA
C2:
NO
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