HsaINT0063313 @ hg38
Intron Retention
Gene
ENSG00000085265 | FCN1
Description
ficolin 1 [Source:HGNC Symbol;Acc:HGNC:3623]
Coordinates
chr9:134913016-134913613:-
Coord C1 exon
chr9:134913581-134913613
Coord A exon
chr9:134913144-134913580
Coord C2 exon
chr9:134913016-134913143
Length
437 bp
Sequences
Splice sites
5' ss Seq
CAGGTGACT
5' ss Score
6.6
3' ss Seq
TCCCCGGGTTCCCTTCCCAGGCC
3' ss Score
10.22
Exon sequences
Seq C1 exon
GAGACGCTGGGCAGTCTCAGTCGTGTGCGACAG
Seq A exon
GTGACTGATCACACCCTGACCTCGGTACCCAAGCCTTGCCCCCACCCCTGGGGCCAGCTGCACACGTTCACGCTACGGAATCTAAGGACAGAACCCTGTCTGCACCTATCATCCCCCCCTCAATCACTCGAGTAATGGGCAGCTATCACCTGAATCCCTTCCATGACAACCTGGGCTCTACTATTATCTACCCTAGAAGGCCGGGTGCCCAGGAGGCAAAGGTGGGGCAGACACTGGGAGGTGGGAGGGTCGGCAGACTGGGTGTGGGCATCACAGCTGCGTGGCCCTGGGGGCCGTGTCCCTGTCCAGGCCTCGGAGTCCTGCTCGGTCCGCACAGAAGCCTGTGGCCCTCCTCCTCCCTCCTGGGCCTCCCTCCCACTGCCCCTGTCCTGCCCAGGGCCCCCGTCCTGCAGCCATTCCCCGGGTTCCCTTCCCAG
Seq C2 exon
GCCCACGCAACTGCAAGGACCTGCTAGACCGGGGGTATTTCCTGAGCGGCTGGCACACCATCTACCTGCCCGACTGCCGGCCCCTGACTGTGCTCTGTGACATGGACACGGACGGAGGGGGCTGGACC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000085265:ENST00000371806:5
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.750 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0139113=Collagen=PD(11.5=58.3),PF0014713=Fibrinogen_C=PU(0.1=0.0)
A:
NA
C2:
PF0014713=Fibrinogen_C=PU(19.7=97.7)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
No conservation detected
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