Special

GgaINT0124105 @ galGal4

Intron Retention

Gene
Description
solute carrier family 27 (fatty acid transporter), member 4 [Source:HGNC Symbol;Acc:HGNC:10998]
Coordinates
chr17:4977891-4978480:-
Coord C1 exon
chr17:4978322-4978480
Coord A exon
chr17:4977961-4978321
Coord C2 exon
chr17:4977891-4977960
Length
361 bp
Sequences
Splice sites
5' ss Seq
TCGGTACGT
5' ss Score
10.06
3' ss Seq
GTCTCCTCATTCCTCCCCAGATA
3' ss Score
9.8
Exon sequences
Seq C1 exon
CTATGAAGGAGGTGCAGTCCTCCATGGAGAAGTCTGTCCATCTCTTCTGGTCAGGAGAAGGAAGCCCTGAGTCCGCACTTTCTGGTGCAAAGCACCTGGATCCCCTCCTGCAGACAGCTCTTCGACAGCAGCCAGATCCCCCTGAGAAGGGCTTTCTCG
Seq A exon
GTACGTGGTCAGCTTTTGGGAGCCAAACTCCTGGTGGTATTTCCGAGGATCATCTGGTCACAACACTGGCAAGAATATCTGCTCAGGATGCTGAGGGCAGACTTCAGCAGCAGAGCCTGGAATGTTTGAAGGGGGGCTGAAGCCTGGCTGCATGTGGTTCAGTATCATGTGCCCTCCATGTGTTCAAACAGGCCTGGGGTGAACCCAGCATGTTCTGTATCACATAACAAAATGTATTTTGATGTGATCAGAGTATGCTTTGACTTGTCCCCACCTTCTGCTTCAGCCAGCTCCTCCTGGATCAGGTGCAGTGATCTAGGTCACGCTGCATGTGTGACCTTGTCTCCTCATTCCTCCCCAG
Seq C2 exon
ATAAACTCTTCTATATCTATACCTCTGGCACTACGGGAATGCCCAAGGCTGCTATTGTGGTCAACTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000004965:ENSGALT00000007962:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=FE(12.2=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(5.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTATGAAGGAGGTGCAGTCC
R:
TGACCACAATAGCAGCCTTGG
Band lengths:
222-583
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]