RnoEX6020597 @ rn6
Exon Skipping
Gene
ENSRNOG00000053691 | Lama5
Description
laminin subunit alpha 5 [Source:RGD Symbol;Acc:621023]
Coordinates
chr3:175575149-175575736:-
Coord C1 exon
chr3:175575602-175575736
Coord A exon
chr3:175575381-175575515
Coord C2 exon
chr3:175575149-175575286
Length
135 bp
Sequences
Splice sites
3' ss Seq
CTCTCCCTGTATGCCCATAGCTT
3' ss Score
7.97
5' ss Seq
TCCGTAAGT
5' ss Score
10.27
Exon sequences
Seq C1 exon
TATGTGGCTGCAGTCCAGCAGGGACCTTGCCTCAAGGCTGTGACGAGTCTGGCCATTGCCAATGCCGACCTGGCTTTGATGGTCCTCACTGTGACCGCTGCCTTCCAGGATACCATGGGTACCCCGACTGTCATG
Seq A exon
CTTGTGCCTGTGACCCTCGGGGGTCCCTGGATCAACAGTGTGGAGCGGGTGGTTTGTGCCACTGCCGTCCTGGCTACACGGGCGCCACTTGTCAGGAATGTAGCCCCGGATTCTACGGCTTTCCCAGCTGCATCC
Seq C2 exon
CTTGCCACTGCTCTGCCGATGGCTCCATGCATACAACCTGTGACCCTACAACTGGCCAGTGTAGGTGCCGTCCCCGAGTGACAGGACTTCGTTGTGATATGTGTGTGCCGGGGGCCTATAACTTCCCCTACTGCGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000053691-'19-16,'19-15,20-16=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF0005319=Laminin_EGF=WD(100=97.8)
A:
PF0005319=Laminin_EGF=PD(0.1=0.0),PF0005319=Laminin_EGF=WD(100=97.8)
C2:
PF0005319=Laminin_EGF=PD(0.1=0.0),PF0005319=Laminin_EGF=PU(91.8=95.7)
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGCAGGGACCTTGCCTCAAG
R:
TAGGGGAAGTTATAGGCCCCC
Band lengths:
249-384
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]