Special

GgaINT0145556 @ galGal4

Intron Retention

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr28:366462-366963:+
Coord C1 exon
chr28:366462-366689
Coord A exon
chr28:366690-366837
Coord C2 exon
chr28:366838-366963
Length
148 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
3' ss Seq
TGTTTTACCTTCATGCACAGATG
3' ss Score
8.16
Exon sequences
Seq C1 exon
ATGTGCGTGTGGAACAGTGCTACATGAAGTGGGATGAAGATGAGTGCACAGAGCCTCTGCCGGGCAAGTACCGGATCGACATGTGCTGCTGTTCTGTGGGCTCAGCCTGGGGCATCGATTGTGAAGAATGTCCTAAGGTTGGTTCTAATGAGTACAAGGCCATCTGCCCAAGGGGACCTGGCTTTGCCAACCGAGGGGACGTGCTTTCAGGCAGGCCCTTCTACAAAG
Seq A exon
GTAAGAAGAAAGAGAGGAGCTGCTAATTGTAGGCTGTCCTCAGCCCATCTCAACTACAGCTCAAGGAAGCTGCTCCCTGCTCTGGGATCCTAAGTTCATTGCAGACATCCCCTCCCTGAAGCACTTACTGTTTTACCTTCATGCACAG
Seq C2 exon
ATGTGAATGAATGTAAAGTCTTCTCTGGCCTGTGCACTCATGGGACATGTCGAAACACCATTGGCAGCTTCAGATGTATCTGTGGCAATGGCTTTGCTCTGGATGCTGAGGAAAGGAACTGCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000327:ENSGALT00000000433:24
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0068312=TB=WD(100=54.5),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGATGAGTGCACAGAGCCTCT
R:
TTCGACATGTCCCATGAGTGC
Band lengths:
245-393
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]