Special

HsaINT0039680 @ hg19

Intron Retention

Gene
ENSG00000114270 | COL7A1
Description
collagen, type VII, alpha 1 [Source:HGNC Symbol;Acc:2214]
Coordinates
chr3:48630208-48630696:-
Coord C1 exon
chr3:48630535-48630696
Coord A exon
chr3:48630372-48630534
Coord C2 exon
chr3:48630208-48630371
Length
163 bp
Sequences
Splice sites
5' ss Seq
CTCGTGAGT
5' ss Score
8.41
3' ss Seq
CCCTGATCCCGCATTCCCAGCGG
3' ss Score
4.63
Exon sequences
Seq C1 exon
GGATCAAGAATGCTGACCCTGAGGAGCTGAAGCGAGTTGCCTCACAGCCCACCAGTGACTTCTTCTTCTTCGTCAATGACTTCAGCATCTTGAGGACACTACTGCCCCTCGTTTCCCGGAGAGTGTGCACGACTGCTGGTGGCGTGCCTGTGACCCGACCTC
Seq A exon
GTGAGTTCCTGCCCACACGGTGTACCCTGACCTAGACCCCGGACCCCAATCCCCACTTGGCAGTGCTGATTCCATCCTATGTGCTCCTGACCCCGACCCCAACTCTGCATCATACATGCCCACCCCAATCCTCCTGCCTGATCCCCTGATCCCGCATTCCCAG
Seq C2 exon
CGGATGACTCGACCTCTGCTCCACGAGACCTGGTGCTGTCTGAGCCAAGCAGCCAATCCTTGAGAGTACAGTGGACAGCGGCCAGTGGCCCTGTGACTGGCTACAAGGTCCAGTACACTCCTCTGACGGGGCTGGGACAGCCACTGCCGAGTGAGCGGCAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114270-COL7A1:NM_000094:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.218 A=NA C2=0.455
Domain overlap (PFAM):

C1:
PF0009223=VWA=PD(20.8=65.5)
A:
NA
C2:
PF0004116=fn3=PU(57.0=89.1)


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:
AGCCCACCAGTGACTTCTTCT
R:
CCGTCAGAGGAGTGTACTGGA
Band lengths:
246-409
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