Special

HsaINT0152130 @ hg38

Intron Retention

Gene
ENSG00000167114 | SLC27A4
Description
solute carrier family 27 member 4 [Source:HGNC Symbol;Acc:HGNC:10998]
Coordinates
chr9:128350484-128352747:+
Coord C1 exon
chr9:128350484-128350575
Coord A exon
chr9:128350576-128352637
Coord C2 exon
chr9:128352638-128352747
Length
2062 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACT
5' ss Score
8.63
3' ss Seq
GGCCATCCCTCTGCCTCCAGGAA
3' ss Score
9.58
Exon sequences
Seq C1 exon
GTATTACCGCATGGCTGCCCTGGTGTACTATGGATTCCGCATGCGGCCCAACGACATCGTCTATGACTGCCTCCCCCTCTACCACTCAGCAG
Seq A exon
GTAACTCTAGGGCTGTCACACAGCCTCCAGCACCTGCCAGGTCTCTAGGAACCCCACCCCCATCAGGCAGTGTGCTGCAGTAGAAACACACAGCTTTGGGCCAGGCGCAGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCAAGGTGGGCGGATCACTTGAGGCCAGGAGTTCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAGTACAAAAAATTAGCCAGGTGTGGTGGCTCATGCCTGTAGGCCCAGCTACTCGGGAGGGTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGCAACAGTACAAGACTCTGTCTCGGAAAAAAAAAAAAGAAAGAAATTATCTGGGTGTGGTGGCGTGTGCCTGTAGTCCCAGCTATCTGTGAGGCTGAGGCACGAGAATTGCTTGAACCTGGGAGGCAAAGGTTGCAGTGAGCTGAGATCACGCCACTGCATTCCAGCCTGGGCAACAGAGCGAGACACTGTCTCAAAAAAAAAAAAAATTAGCTGGGTCTGGTGGCGTGTGCCTGTAATCCCAGCTACCTGTGAGGCTGAGGCATGAGAATTGCTTGAACCTGGGAGGCAAAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACACTGTCTCAAAAAAAATAAAAATAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGTGAGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGTTAACATGGTGAAACCCTGTCTCTACTAAAAGTACAAAAAGTAGCTGGGCTTGGTGGCGGGTGCCTGTAATCCCAGCTACCCAGGAGGCTGAGGCAGGAGAATGGTTTGAACCCAGGAGGCAAAGGTTGCAGTGAGCCTAGATCGTGCCATTGCACATCAGCCTGGGTGACAGGGCAAGACTCTGTCTCAAAATAAATAAATAAATTAATTTAATTTAATTTAAAAATAAAAATAAACAGGATTAGCCAGGCGTGGTGCACATGCCTATGGTCTCAGCTACTGGGAAGGCTGAGACAGGAGAATCACTTGAGCCTGGGAGTTTAAGGCCAGCCTGGGCAACATGGTGAGACCTGTCTCTAAAAAAAATTTTGTTTTAGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGATGAAACCCCATCTCTACTAAAAATACAAAAAAAAAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGATGATGCAGGAGAATGGCATGAACCCGGAAGGCGGAGCTTGCAGTGAGCCGAGATGGCATCACTGTACTCCAGGCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGTTGTTTTAAATTGAAAAAAGGATGAGCACACCAGCCTCACAGTGTGTGTGGCAGTGTCCCACGGGGCATCTGGGCCTGTCTCATTTCAGTTTGTTTCCACAGATATGCATGGCATTGCTGCTTGTTTGTAGGGGCTTAAGGGAAGACAGCTTGAATAAATATAGCTCCTGCCCTCCAGGTGCTTAGAGTCGGGTGTATATGTGAGTGTAGGAGAGAGGCAGGGAGCAAGAGGGCAGCACCAGGGAAGAGCCTGGTGATGGAAGCCGGGGAGGCTTCTTGGAGGAGGTCACCCAAGGCAGGCAGATGTGAGGTGCAGAAGCCTGCAGGGCAGCACAAGCCTGCCTGGCTGGATGGCAGTATCACTGATTTGGGGCCGGGGAGGGTCTTCATCTCGCTGACCCTCAGGGGCCATCCCTCTGCCTCCAG
Seq C2 exon
GAAACATCGTGGGAATCGGCCAGTGCCTGCTGCATGGCATGACGGTGGTGATTCGGAAGAAGTTCTCAGCCTCCCGGTTCTGGGACGATTGTATCAAGTACAACTGCACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167114:ENST00000300456:6
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:
PF0050123=AMP-binding=FE(7.2=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(8.3=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains