Special

GgaINT0145553 @ galGal4

Intron Retention

Gene
Description
fibrillin 3 [Source:HGNC Symbol;Acc:HGNC:18794]
Coordinates
chr28:365083-365750:+
Coord C1 exon
chr28:365083-365133
Coord A exon
chr28:365134-365624
Coord C2 exon
chr28:365625-365750
Length
491 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAG
5' ss Score
9.06
3' ss Seq
TTTTGCTTTGCTGCCAACAGATG
3' ss Score
9.03
Exon sequences
Seq C1 exon
ATACTGCCTGTCCCCGGGGCTATGCCAGGATGAAGGGGGTTACTTGTGAAG
Seq A exon
GTAAAGTGCTGCAGGACACAGAAGACTTTTTAACTGGGAACATAGTCATTGTTTATTTGCTATTTTTATGCATCTTTGAGTTTGGACACAGCCTGCTGAAGCCCTGTGATTTTTGTGCTGTCTCTTGCTTTGGCACCTGCCCTGAGCACTGCAGCTGAGGTATGGGCAGTATGTAACACCAGTGTGTTCAGACACAGTACTGATGTCTGTGAGTCCTGGTGTTTCTCTGTCAGCACTGTATCAACTGCGGACCTGTGCAATAGGACTGCCCTCTGCCTGCTCATGTCTGACACTGTGATACAGCCTCCTTGCAAACATCTCTGCACGTGACTGTGGCTGTGCCTGGAGGATGTTTTGCAGTGTGACAAGCCACCAGTTTCAGCCAGTTGGGCAGCTCTGGGCTCTTTCTGGATCCCTAGGAGCCCCTCAAAGCCATGGTAGTCGTGACTATGTGCCACTCTCATGCCTGCCTTTTGCTTTGCTGCCAACAG
Seq C2 exon
ATGTGAATGAGTGTGATGTCTTTCCTGGTGTCTGCCCAAATGGTCGCTGTGTGAACACAGCTGGCTCCTTTCGGTGTGAGTGTCCAGAAGGATTGACCCTCGATGGCACTGCTAGGACGTGTGTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000327:ENSGALT00000000433:22
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=PD(17.1=38.9),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.3)


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:
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]