DmeEX6015833 @ dm6
Exon Skipping
Gene
FBgn0267348 | LanB2
Description
The gene Laminin B2 is referred to in FlyBase by the symbol DmelLanB2 (CG3322, FBgn0267348). It is a protein_coding_gene from Dmel. It has 3 annotated transcripts and 3 polypeptides (1 unique). Gene sequence location is 3L:9614914..9623980. Its molecular function is unknown. It is involved in the biological process described with 11 unique terms, many of which group under: anatomical structure development; cellular process; system development; cellular component organization; biological adhesion. 17 alleles are reported. The phenotypes of these alleles manifest in: organ system; germ layer derivative; extracellular region; pericardial cell; embryonic pericardial cell. The phenotypic classes of alleles include: viable; lethal - all die before end of pupal stage; phenotype; increased mortality during development.
Coordinates
chr3L:9622423-9623980:+
Coord C1 exon
chr3L:9622423-9622759
Coord A exon
chr3L:9622817-9623117
Coord C2 exon
chr3L:9623179-9623980
Length
301 bp
Sequences
Splice sites
3' ss Seq
TTCGTAAAATTTCTTGACAGGAT
3' ss Score
6.32
5' ss Seq
TGGGTAAGA
5' ss Score
8.91
Exon sequences
Seq C1 exon
AGCTGAACAGCAGCAACTGGAGGACATCGAGCTGCTAGAGCGAGCCAAGGCTGCCCACGACAAGGCTACCAAGGCAGTGGAACAGGGCGACAATACCCTAAAGGAGGCCAACAATACCTACGAGAAGTTGGCCGGCTTCCAGTCGGATGTCCAGCGCTCTTCTGAGAGTGCGGAGAAAGCCCTGCAGACGGTGCCCAACATCGAGAAGGAGATTCAGAATGCGGAAAGCCTGATCAGCCAGGCGGAGGAGGCTCTCGATGGAGCCAATAAGAATGCCAACGAGGCCAAGAAGAATGCCCAGGAGGCGCAGCTGAAGTATGCCGAACAGGCTTCCAAG
Seq A exon
GATGCTGAGCTGATCCGCCGCAAAGCCAATGAGACCAAGGTGGCTGCCCGCAATCTGCGCGAAGAGGCCGACCAACTGAATCATCGCGTGAAACTCACCGAAATGGACATCTTCAAGCTGGAGGAGAGCTCGACCAAGGACGACAATCTGGTGGACGACGCCAAGCGAAAGGTGGGTCAGGCCAAGGCCGATACCCAGGAGGCCCAGAAGCAGATCGAGAAGGCCAATGCCGACCTGACGGCCATCAAGGATGAGCTGGAGAATCTGAAGGACATCAACACGGGCGATTTGGATAGATTGG
Seq C2 exon
AGAATCGTTTGGCCACTGTGGAGGGTGAGATCAATCGCGTCAACCTGACGGGACGCATCGAAAAGTACCGGGAACAGCGCACCATTCAGAAGAATCTGATCGACAAGTACGATGCCGAGCTGAGGGAGCTCAAGGATGAAGTCCAGAATATTGGACTTATTTCCAAGGCTCTCCCCGATAGCTGCTTCAGTCGCAATCGCCTGGAACCCTAGAGCTCTGCGAACAACCCCACTTCCCATAACAACTACTTCAATTTTAACTAAGAACGAAGATCTGAGACGAGACGAACAAATCAGATTTATGATAGAACGTAGACGTTGAATGAAATTATGTAATTTTAGTGCCTTAGCCGAAATATTCTGTTTAGTGACCCAGCCCAAGGATCCAAGGATCCACAAAGGAGACCAACTGAGCAACGTTAAGCTTTAACGCATCATCGTTCGCCTACTGTATGCCATATACTATAATGATACAACGGATACAAGAGGATGGATGATGGC
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0267348-'19-11,'19-10,20-11=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (No Ref, Alt. Stop)
No structure available
Features
Disorder rate (Iupred):
C1=0.912 A=0.653 C2=0.043
Domain overlap (PFAM):
C1:
NO
A:
NO
C2:
NO
Main Inclusion Isoform:
FBpp0076111

Main Skipping Isoform:
NA
Other Inclusion Isoforms:
FBpp0311281
Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg19)
No conservation detected
Mouse
(mm9)
No conservation detected
Chicken
(galGal3)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GTGCCCAACATCGAGAAGGAG
R:
TTGCGACTGAAGCAGCTATCG
Band lengths:
343-644
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Neural diversity
- Neurogenesis
- Neuronal activity
- Splicing factor regulation (brain)
- Splicing factor regulation (SL2)