Special

HsaINT0039002 @ hg19

Intron Retention

Gene
ENSG00000134871 | COL4A2
Description
collagen, type IV, alpha 2 [Source:HGNC Symbol;Acc:2203]
Coordinates
chr13:111155468-111155828:+
Coord C1 exon
chr13:111155468-111155629
Coord A exon
chr13:111155630-111155729
Coord C2 exon
chr13:111155730-111155828
Length
100 bp
Sequences
Splice sites
5' ss Seq
AAGGTAACA
5' ss Score
8.92
3' ss Seq
ACGTCTTGTTTGTGTTGCAGGGC
3' ss Score
10.33
Exon sequences
Seq C1 exon
GTTATCGGGGCCCACCAGGGCCACCAGGTTCTGCTGCTCTTCCTGGAAGCAAAGGTGACACAGGGAACCCAGGAGCTCCAGGAACCCCAGGGACCAAAGGATGGGCCGGGGACTCCGGGCCCCAGGGCAGGCCTGGTGTGTTTGGTCTCCCAGGAGAAAAAG
Seq A exon
GTAACAGTGCCCATGGCCATGGGCCAGCAGCCCTGGCCACAGTGAGAGGAGCCCCCTCCCCACAGACTTTCGTGTCCCTAACGTCTTGTTTGTGTTGCAG
Seq C2 exon
GGCCCAGGGGTGAACAAGGCTTCATGGGGAACACTGGACCCACTGGGGCGGTGGGCGACAGAGGCCCCAAGGGACCCAAGGGAGACCCAGGATTCCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000134871-COL4A2:NM_001846:42
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(13.2=21.8),PF0139113=Collagen=PD(74.6=85.5),PF0139113=Collagen=PU(23.1=27.3)
A:
NA
C2:
PF0139113=Collagen=FE(50.8=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:
TTATCGGGGCCCACCAGG
R:
GAATCCTGGGTCTCCCTTGGG
Band lengths:
256-356
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