Special

GgaINT0027939 @ galGal4

Intron Retention

Gene
Description
fibrillin 1 [Source:HGNC Symbol;Acc:HGNC:3603]
Coordinates
chr10:9682342-9682798:-
Coord C1 exon
chr10:9682673-9682798
Coord A exon
chr10:9682465-9682672
Coord C2 exon
chr10:9682342-9682464
Length
208 bp
Sequences
Splice sites
5' ss Seq
TAGGTAGGT
5' ss Score
7.92
3' ss Seq
TCTGGTTTTGCTTATTTTAGATC
3' ss Score
9.02
Exon sequences
Seq C1 exon
ATATTGATGAGTGCAAGGTTATCCACGATGTCTGCCGTAATGGGGAATGCATCAATGAAAGGGGATCTTACCGTTGTCACTGCAATCTTGGCTATACTACAGATATAACTGGCACTCTTTGCATAG
Seq A exon
GTAGGTTTTTCGTTATGTTCTATGAATATAAAGTTTATTATGCTGTATGTACATAAAGCCTATTAGTAAGAGATGGCTTGTGGAAAGAAATACAAAAACTTTGAAAAATGAGGGAAAAAATGTCCTTCATTAAGAGGTTTTGAGCATTTTAAAAAACATCACAAATGTCGGTCGTTATCATGAAGATATCTGGTTTTGCTTATTTTAG
Seq C2 exon
ATCTGAATGAATGTAATGAGTCCCCCAAACCTTGCAATTTCATCTGCAAAAACACAGAAGGGAGCTTCCAGTGCTCATGTCCGAAAGGGTACATCCTTCAAGAAGATGGGAGAAGCTGCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004960:ENSGALT00000007955:57
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:
PF0764510=EGF_CA=WD(100=95.3),PF0764510=EGF_CA=PU(0.1=0.0)
A:
NA
C2:
PF0764510=EGF_CA=WD(100=95.2),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:
TGATGAGTGCAAGGTTATCCACG
R:
TTTGCAGCTTCTCCCATCTTCT
Band lengths:
244-452
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]