Special

HsaINT0152128 @ hg19

Intron Retention

Gene
ENSG00000167114 | SLC27A4
Description
solute carrier family 27 (fatty acid transporter), member 4 [Source:HGNC Symbol;Acc:10998]
Coordinates
chr9:131110824-131112660:+
Coord C1 exon
chr9:131110824-131110982
Coord A exon
chr9:131110983-131112590
Coord C2 exon
chr9:131112591-131112660
Length
1608 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
CTCGCGTCTGTTTTCTTTAGATA
3' ss Score
9.54
Exon sequences
Seq C1 exon
CCATCTGTGAGGTCCATGCCAGCCTGGACCCCTCGCTCAGCCTCTTCTGCTCTGGCTCCTGGGAGCCCGGTGCGGTGCCTCCAAGCACAGAACACCTGGACCCTCTGCTGAAAGATGCTCCCAAGCACCTTCCCAGTTGCCCTGACAAGGGCTTCACAG
Seq A exon
GTGGGCTCCATCCCCTCCCCATAGAGGGGCTCTCACACAGGCCCTGGACAGAGCACTGGCCTCAGTGCCAGAAGGAGGCTTTTCTGGAAACTTGCCATGTGCCTGGAACATGTCACGTCACCTCCCTTTTTCCATCTGGAAAATGGTGACAGTAAACCTGGGCCACTCCAGGGTTACTGTGAAGGTGACATGAGCTGATGTGTATCAGTGCCAGATACAGGGCTGAGAACACAGGAGCTCACAAAGTCCAGTGTGATTTGTTGAACAAGCCTTCATTGATGCCTAATGGGCAGAATCCTGTGGACTCCGGGAACCTGCCTGGTCTGGGCTTTGGTTGGGGTTGGGTGGGAGGGTGGGTGAGGAGCAAGACCCTTTGTATATTCATCAAGTGCCTCTTCAGTGCAGGACACTTCAGGATCTCCAGCTGTGATCCTCTCCCAGCACTGTGCTGCCTCCCTGACCCCACCTCCAGGCAGCCTTCCTGAGCCTCTCACCCCTCTTCTTTTATACTGTAGCCTACCTGGTTCTTCTGCTCTTCTCATTCTCTTTCCTGTGAAGCCACATTGCCTGGTGGCTCAGAGCTTGGGCTGTCGAGTCAGATCCGAGTTTATATCCTGGTTCTACTGCTTCCTTTGTGTGAACCCTGACACCTGCCCTGCCCTTGGAGCCTCAGTTCCCACAGCCATAAAACTGGGGACAGTAGCAGAACCTACTCTATGGGGTATCTTTGAGGGTTGAAAAAAATACAGTGGGGCCAGTCCTGAAGCTAGGGTGTGGCAGGAGGGGCTCAGTAACTGGTCATTGTCATCAGCACTGTTTAACTTCTCTCTTGTATGTGAATCTGGTCTCTTGGGTGCATTTGTCAGCTGCTTGAGGGCAGGGACTCTGGCTGGTTGCTCTGGTGCCCTCATAGTGCCTAGGGCTGGCAAACAGCAGGCAGGCAGAGAGCATGAGGTGTCTCGGCAGGCATTCTAAACACGTGGAGTCTGCCTGTGGAGTTCCTGACCTCCAGGGAACCTCAAGTCTGGTAGGGCCGAGCCTCACATAGAAACTCTAACGTGGCAATCCCTGTCGAGGGCTGCAGAGTGGGACAGATCAATGCTCAGCAGTGCGGAAGCTACCTCAACACCCCACTTCCTGCAGCTAATGCCTCCCTGTGCTCTATGACTTGGGGCAGGTGTCACCTTTATCGTGAAGCCCACCTGGCACCACCTCCCCTCCTGCAAGCTTGGGCCAAATGTGGCTACTGGGTTTCAACAGGTCCTGTGCCCTCCCTCGGCACTTGTTGCTTAGTATTGGAATTGCCTGTGTCCTCATCTGACTGTTCCACTGAGCTGTGACTGCCAAGAGGGCCAGGCCCGTGCCCATCTTACTCACTGATGTCTCTCTCCACCAGGGCCTAGCACAGAGCAAGGGCCCAGGAAATATTTGTTGGAATGGATGCCGGTGTTAGAGCTGAATGGTATCTGAGGTTATCAGAACAGGCTTCCTAGCAAGGGTGTGATGGGAACAGGTGTTGAAGGGTGCACACCTGCAGGTGTCCATTTGTGTGACCCTTTGCCCAGCCCTGAGCTGCCCCCGACAGCCACTCGCGTCTGTTTTCTTTAG
Seq C2 exon
ATAAACTGTTCTACATCTACACATCCGGCACCACAGGGCTGCCCAAGGCCGCCATCGTGGTGCACAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167114-SLC27A4:NM_005094:4
Average complexity
IR-S
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
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CATCTGTGAGGTCCATGCCAG
R:
CTGCTGTGCACCACGATGG
Band lengths:
228-1836
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains