DmeALTA0006905-1/2 @ dm6
Alternative 3'ss
Gene
FBgn0011259 | Sema-1a
Description
The gene Semaphorin 1a is referred to in FlyBase by the symbol DmelSema1a (CG18405, FBgn0011259). It is a protein_coding_gene from Dmel. It has 8 annotated transcripts and 8 polypeptides (6 unique). Gene sequence location is 2L:8542147..8672041. Its molecular function is described by: protein binding; chemorepellent activity; heparin binding; semaphorin receptor binding. It is involved in the biological process described with 13 unique terms, many of which group under: negative chemotaxis; negative regulation of cellular component movement; stem cell differentiation; positive regulation of cellular component movement; cell recognition. 57 alleles are reported. The phenotypes of these alleles manifest in: cellular anatomical entity; non-connected developing system; transverse nerve; adult head segment; motor neuron. The phenotypic classes of alleles include: viable; increased mortality during development; phenotype; increased mortality. Summary of modENCODE Temporal Expression Profile: Temporal profile ranges from a peak of moderately high expression to a trough of very low expression. Peak expression observed within 12-18 embryonic stages.
Coordinates
chr2L:8661359-8662646:+
Coord C1 exon
chr2L:8661359-8661487
Coord A exon
NA
Coord C2 exon
chr2L:8662457-8662646
Length
0 bp
Sequences
Splice sites
5' ss Seq
AAGGTGATT
5' ss Score
5.88
3' ss Seq
AGGTCCCCAAATATCTGCAGATA
3' ss Score
4.72
Exon sequences
Seq C1 exon
GCAAAATCAATTCAAAGGATGCCAACGCTGGGGAGCAGAAGGGCTTCCGCAACGACATGGACTTATTGGATTCGCGACGCCAGAGCAAGGATCAGGAAATAATCGACAATATTGATAAGAACTTTGAAG
Seq A exon
NA
Seq C2 exon
ATATAATCAACGCCCAGTACACTGTGGAGACCCTCGTGATGGCCGTTCTGGCCGGTTCGATCTTTTCGCTGCTGGTCGGCTTCTTTACAGGCTACTTCTGCGGTCGCCGTTGTCACAAGGACGAGGATGATAATCTGCCGTATCCGGATACGGAGTACGAGTACTTCGAGCAGCGGCAGAATGTCAATAG
VastDB Features
Vast-tools module Information
Secondary ID
FBgn0011259-23-25,23-24-1/2
Average complexity
Alt3
Mappability confidence:
NA
Protein Impact
Protein isoform when splice site is used (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.320 A=NA C2=0.172
Domain overlap (PFAM):
C1:
PF0143720=PSI=PD(7.8=11.4)
A:
NA
C2:
NO
Main Inclusion Isoform:
FBpp0079302

Main Skipping Isoform:
FBpp0302962

Other Inclusion Isoforms:
FBpp0302963, FBpp0302964
Other Skipping Isoforms:
FBpp0292880, FBpp0292881, FBpp0292882
Associated events
Conservation
Human
(hg38)
No conservation detected
Human
(hg19)
No conservation detected
Mouse
(mm10)
No conservation detected
Mouse
(mm9)
No conservation detected
Rat
(rn6)
No conservation detected
Cow
(bosTau6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TTATTGGATTCGCGACGCCAG
R:
CGAGGGTCTCCACAGTGTACT
Band lengths:
103-121
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)