Special

GgaINT0050394 @ galGal4

Intron Retention

Gene
ENSGALG00000011052 | SLC38A11
Description
solute carrier family 38, member 11 [Source:HGNC Symbol;Acc:HGNC:26836]
Coordinates
chr7:19516782-19517381:+
Coord C1 exon
chr7:19516782-19516852
Coord A exon
chr7:19516853-19517219
Coord C2 exon
chr7:19517220-19517381
Length
367 bp
Sequences
Splice sites
5' ss Seq
TTGGTAAGT
5' ss Score
10.47
3' ss Seq
AACTATTATGTGTATTTCAGCAT
3' ss Score
6.98
Exon sequences
Seq C1 exon
ACCCAAATCAGAAAATGCATGGATATTTGCAAAATCAAATGCAATACAAGCTGTTGGGGTGATGTCTTTTG
Seq A exon
GTAAGTCATTTTTGTATTTTCAGTCTTCAGATCAACTTTAAGAAATGACTTAGATTTTTTTGAACCTAGAATTTGTGTTGTTTTGTTTTTAATTTTGGGGGTGGTGTTTTTTTTGATACTCATGGGGAAGAGGGAAAGAAACACCGTGGCGTTTTGGGGTAATGTAATCAGAGTCATCTCAAAATGACTATAAACTTTCATCAAATAAGTAGAAGTTCCATTCCTTGTAGGTTTAATGTTTGTGTTCAGTAATGAGTGGTATCAAACTGCTGTGTCTCTCTTACCTTGGTGTATGCACTTCATTAATTTATTTCATATGTACATATGTATGAATTAATGTTTCCTTGAACTATTATGTGTATTTCAG
Seq C2 exon
CATTCATCTGCCATCATAACAGCTTTTTAATATATGGCTCTCTGAAAGAACCCACATTAAACAACTGGTCTCGAATCACACATATGTCTGTTTTACTTGCTGTTGTTATCAGTGTACTATTTGCTGCATGTGGATACATGACTTTTACAGGATACACTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011052:ENSGALT00000018002:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0149013=Aa_trans=FE(6.2=100)
A:
NA
C2:
PF0149013=Aa_trans=FE(13.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


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:
ACCCAAATCAGAAAATGCATGGA
R:
TCAGTGTATCCTGTAAAAGTCATGT
Band lengths:
231-598
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]