HsaINT0159709 @ hg38
Intron Retention
Gene
ENSG00000149418 | ST14
Description
suppression of tumorigenicity 14 [Source:HGNC Symbol;Acc:HGNC:11344]
Coordinates
chr11:130197841-130198418:+
Coord C1 exon
chr11:130197841-130197945
Coord A exon
chr11:130197946-130198307
Coord C2 exon
chr11:130198308-130198418
Length
362 bp
Sequences
Splice sites
5' ss Seq
GCAGTGAGT
5' ss Score
7.39
3' ss Seq
CTCCCCTTACCCCACTCCAGGTT
3' ss Score
7.81
Exon sequences
Seq C1 exon
CATGCCCGGGGCAGTTCACGTGCCGCACGGGGCGGTGTATCCGGAAGGAGCTGCGCTGTGATGGCTGGGCCGACTGCACCGACCACAGCGATGAGCTCAACTGCA
Seq A exon
GTGAGTCAGGCTGGGAGCCCCGGTCTCCCCACCCTCCTTCCCCACCCTGCCCGCGTCCCATGGCCCTGCTGGCTGACTGCCGAGGCAGAAAGGCCGGAGGTGGTGGGAGTTTTTGCTCTCGGCCCTGTGTAGAGACCTCTGGCCCCACTCCCCACCCTGCCATATGGAGATCTTGGCCTGTGGGGCAGGTGGTGGGGTATCTCGGAAGTGCTGAGGTCAGCTTGGTAGCTGGTGGAGCAGGGCCCCTTGGGCCTCTCTGTAGATCAGAAAGCGGTCCCCAGGTAGCTCTGATCGCCTGGGCATCCTGGGGAAGCAGTGAGTGATGAGGGCCTCACGGCCGACCTCCCCTTACCCCACTCCAG
Seq C2 exon
GTTGCGACGCCGGCCACCAGTTCACGTGCAAGAACAAGTTCTGCAAGCCCCTCTTCTGGGTCTGCGACAGTGTGAACGACTGCGGAGACAACAGCGACGAGCAGGGGTGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000149418:ENST00000278742:12
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:
PF0005713=Ldl_recept_a=PD(94.4=94.4),PF0005713=Ldl_recept_a=PU(0.1=0.0)
A:
NA
C2:
PF0005713=Ldl_recept_a=WD(100=97.4),PF0005713=Ldl_recept_a=PU(0.1=0.0)
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:
GCAGTTCACGTGCCGCAC
R:
CTGCTCGTCGCTGTTGTCTC
Band lengths:
199-561
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains