Special

HsaINT0039376 @ hg19

Intron Retention

Gene
ENSG00000080573 | COL5A3
Description
collagen, type V, alpha 3 [Source:HGNC Symbol;Acc:14864]
Coordinates
chr19:10089250-10089656:-
Coord C1 exon
chr19:10089567-10089656
Coord A exon
chr19:10089304-10089566
Coord C2 exon
chr19:10089250-10089303
Length
263 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGT
5' ss Score
10.9
3' ss Seq
TGAATTATCTCCTCCTTCAGGGA
3' ss Score
9.17
Exon sequences
Seq C1 exon
GGGGAACTGGGACCACCAGGACCCCTTGGGAAAGAAGGGCCAGCTGGACTCAGGGGCTTTCCCGGCCCCAAAGGGGGCCCTGGGGACCCG
Seq A exon
GTGAGTATCTTTGGAGACCCTCCTGCATGTCCCTTAGAGAAGGAAAGGATGGGGGGGTCAGGGGAGGGATGGGGAATAGCATTTGGGGTGCGGGAAATGATGAAAGCAAAAAAAATGGTGGAGGGAACTGGGGAAGGCAGACCCCTCAAAGCTCAGTGTCCAGTCCCAGGAGAGAGGTGGGGACTGTGAGCTCCCCACAGAGGAAGACAGGACCTGGGGACACCTTTGGGAGTCTCTTAACTGTGAATTATCTCCTCCTTCAG
Seq C2 exon
GGACCTACTGGCTTAAAGGGTGATAAGGGCCCCCCAGGGCCCGTGGGGGCCAAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000080573-COL5A3:NM_015719:40
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(10.3=23.3),PF0139113=Collagen=FE(47.5=100)
A:
NA
C2:
PF0139113=Collagen=FE(27.9=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:
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