HsaINT0152131 @ hg19
Intron Retention
Gene
ENSG00000167114 | SLC27A4
Description
solute carrier family 27 (fatty acid transporter), member 4 [Source:HGNC Symbol;Acc:10998]
Coordinates
chr9:131114917-131115513:+
Coord C1 exon
chr9:131114917-131115026
Coord A exon
chr9:131115027-131115303
Coord C2 exon
chr9:131115304-131115513
Length
277 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGC
5' ss Score
9.44
3' ss Seq
CACACCAAGTTCACCCCCAGATT
3' ss Score
1.87
Exon sequences
Seq C1 exon
GAAACATCGTGGGAATCGGCCAGTGCCTGCTGCATGGCATGACGGTGGTGATTCGGAAGAAGTTCTCAGCCTCCCGGTTCTGGGACGATTGTATCAAGTACAACTGCACG
Seq A exon
GTGAGCGAGAGCGGGAAGGGTGAGCTGTCCCTTTCCCCTAGTTACCCTCTTCCCAACTACACTCCGGGGCATCTGTCTTATAGCTGAGGTGGCCAGTCATTCCAAAGGGCTCATTTGTGGCAAAGTTCCCATTGTTCAGATGGGAAGGCTGAGACCCGGAGAGGGAAAGGATGGCATGGCCAGCCCCTGGGGAGAGTAGGGGCTTGAGGGATCAGGAGAATCCTAGTGTAGTGAGGGCAGCCTCTGGAGCCTCGAATCACACCAAGTTCACCCCCAG
Seq C2 exon
ATTGTGCAGTACATTGGTGAACTGTGCCGCTACCTCCTGAACCAGCCACCGCGGGAGGCAGAAAACCAGCACCAGGTTCGCATGGCACTAGGCAATGGCCTCCGGCAGTCCATCTGGACCAACTTTTCCAGCCGCTTCCACATACCCCAGGTGGCTGAGTTCTACGGGGCCACAGAGTGCAACTGTAGCCTGGGCAACTTCGACAGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167114-SLC27A4:NM_005094:7
Average complexity
IR-S
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:
PF0050123=AMP-binding=FE(8.3=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(15.9=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:
GAAACATCGTGGGAATCGGCC
R:
CCAGGCTACAGTTGCACTCTG
Band lengths:
303-580
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)