GgaINT0124112 @ galGal4
Intron Retention
Gene
ENSGALG00000004965 | SLC27A4
Description
solute carrier family 27 (fatty acid transporter), member 4 [Source:HGNC Symbol;Acc:HGNC:10998]
Coordinates
chr17:4974922-4975682:-
Coord C1 exon
chr17:4975518-4975682
Coord A exon
chr17:4975069-4975517
Coord C2 exon
chr17:4974922-4975068
Length
449 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACT
5' ss Score
8.63
3' ss Seq
CCTTCTTTTCTGTCTCTCAGGCA
3' ss Score
11.33
Exon sequences
Seq C1 exon
GGGATGTCCTGGTGATGGACAAATACGGTTACATGTACTTTCGGGACCGCACTGGAGACACATTCCGCTGGAAGGGAGAGAACGTCTCCACTACTGAAGTGGAGGGGACGCTGAGCCGCATCCTCAACCTGACAGACGTGGTTGTGTATGGGGTGGAGATCCCAG
Seq A exon
GTAACTGAGAGGGGAGGGGAGGACAGTGGAGGCAGGCAGGCTGCGGTACTTGGGCGTGTGTCTTGCTTGTCCACATCGTGTCCTTTCACAAGAGGCTGGACAGAGGCTCCTTGTGAGCTGGGAAGAGACTACTGGGAATGTGACTAGCAGGAGCCAAAGAGTTCCCTCTCTCAGGCAGAGGTTTGGCCTGGTCCTGGCTGGTTTGGAAGGGCCCTGAGTCCTTTTGGGATAGGCTGCGAGTGCTGCCTCTGGGAGGAGATGACCATGACCGCAGGGTGTCGCTGGTAAACGTGGCTGTAGGGTGGTGACACAGGCAGTGACACAACTGGACATTTGGTGCTTTCTACAAAGCAGGGAAAGTGCCAGAGGCCTCAGTGCTGTGGGGCAAACAGAAGTGATGCCGCAGGGACAGCGTGCCCAAGAACTCTCCCTTCTTTTCTGTCTCTCAG
Seq C2 exon
GCATTGAGGGGAAGGCAGGAATGGCAGCCATTGCCGACCCAGAGAACTCATGTGACCTGGAGGGCTTTGCCAGCCAGCTGAAAAAGGCCCTGCCGCTGTATGCACAGCCTGTCTTCCTACGGTTCCTGCACGAGGTCTCCAAAACAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004965:ENSGALT00000007962:10
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.036 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0050123=AMP-binding=PD(5.5=42.9),PF131931=AMP-binding_C=PU(30.3=41.1)
A:
NA
C2:
PF131931=AMP-binding_C=FE(64.5=100)
Main Inclusion Isoform:
NA

Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GGGATGTCCTGGTGATGGA
R:
TGTTTTGGAGACCTCGTGCAG
Band lengths:
311-760
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]