Special

GgaINT0071396 @ galGal4

Intron Retention

Gene
Description
low density lipoprotein receptor-related protein 5-like [Source:HGNC Symbol;Acc:HGNC:25323]
Coordinates
chr4:48992661-48993330:+
Coord C1 exon
chr4:48992661-48992844
Coord A exon
chr4:48992845-48993128
Coord C2 exon
chr4:48993129-48993330
Length
284 bp
Sequences
Splice sites
5' ss Seq
TGGGTAAGG
5' ss Score
9.08
3' ss Seq
AGCACTCCTCTTCCTGCCAGGAT
3' ss Score
7.51
Exon sequences
Seq C1 exon
GTGTGAGATCAGACTGTATCGCTGTGGACTGGATTGGGAGGAACCTGTACTGGACGGACGGGGTGGCAGGGCAGGTGCTGGCCACTTCTCTGGAGACCACCTGGCGAGGGAAACCAGAGTACACCATGGTGCTGGATGGAGACTTGGACCAGCCACATTCCCTGGTGCTCCAGCCTCTGGCTGG
Seq A exon
GTAAGGCTGGGGCCAGAGGGCTTGGGGATCTTCTTGCCTAGCCCATTTTCCCCCATAGAAGCAGACAACAGGCTGGGGGAGAGTTGGGTTGGGCTCATCTGGGTGCTGTTGCAGCTGTATGACTGGGGAAGAAGGAGCCCAAGCATCTGCTCCTGCCCTACGCAGAGCTCTCAGTACATCCCTGATGGGATGGGAAACCCTGTGCTACCCCTCTGTGCTGCCCTGTTACTGCCCTGGTACTGGGCTGTGCCAGGTCTGTGGGCCAGCACTCCTCTTCCTGCCAG
Seq C2 exon
GATGCTATACTGGTCAGAGGTGGGGAACCAGCCACGGCTGATGGAGGCCACCATGGATGGAAGGCGGCAGCGTGTGCTGCTGGCGCAGGGCCTGGGCTGGCCCACAGCACTAGCCCTTGACCTCCCCACCTCGAGGCTCTTCTGGCTGGATGAAAAGCTGGGCAGTGTTGGTTCCACACATCTGGATGGCACCGATGTAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000023172:ENSGALT00000037928:25
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=0.015
Domain overlap (PFAM):

C1:
PF0005812=Ldl_recept_b=PU(0.1=0.0)
A:
NA
C2:
PF0005812=Ldl_recept_b=WD(100=61.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Mouse
(mm9)
No conservation detected
Cow
(bosTau6)
No conservation detected
Zebrafish
(danRer10)
LOW PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GAGGAACCTGTACTGGACGGA
R:
TTCATCCAGCCAGAAGAGCCT
Band lengths:
301-585
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]