Special

HsaINT0008649 @ hg38

Intron Retention

Gene
ENSG00000107890 | ANKRD26
Description
ankyrin repeat domain 26 [Source:HGNC Symbol;Acc:HGNC:29186]
Coordinates
chr10:27093349-27093799:-
Coord C1 exon
chr10:27093685-27093799
Coord A exon
chr10:27093523-27093684
Coord C2 exon
chr10:27093349-27093522
Length
162 bp
Sequences
Splice sites
5' ss Seq
AAGGTATAT
5' ss Score
7.84
3' ss Seq
TCTTGGTCTAATACTCCCAGGCT
3' ss Score
3.8
Exon sequences
Seq C1 exon
GACGGCTCTACATTTGGCCTGTGCCAATGGTCATCCAGAAGTAGTAACTCTCCTGGTGGACAGAAAATGCCAGCTCAATGTCTGTGACAACGAAAACAGGACAGCTCTGATGAAG
Seq A exon
GTATATAGTAGCCAGCTCTTTCAGCATCAGATGGATTTGACTTAAATACATAGAATGAAAATGAATTTATCTCATTAAAATATAACTAATTGGTGAAACCTGTGGAGTGTTTATTTTGCATTCCTAGAATTTATGATCTGTTTCTTGGTCTAATACTCCCAG
Seq C2 exon
GCTGTACAATGCCAGGAAGAGAAATGTGCAACTATTCTGCTAGAACATGGTGCTGATCCAAATCTTGCGGATGTCCATGGCAACACTGCTCTTCACTATGCTGTCTATAATGAGGACATATCAGTAGCAACAAAGCTGCTTTTGTATGATGCAAATATTGAAGCAAAAAACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000107890:ENST00000376087:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.026 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF136371=Ank_4=PD(35.8=48.7),PF127962=Ank_2=PU(21.6=41.0)
A:
NA
C2:
PF127962=Ank_2=PD(24.5=39.7),PF0002325=Ank=WD(100=56.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GACGGCTCTACATTTGGCCTG
R:
GCAGCTTTGTTGCTACTGATATGT
Band lengths:
254-416
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development