Special

HsaINT0049978 @ hg38

Intron Retention

Gene
Description
dynein axonemal heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]
Coordinates
chr6:38842368-38842903:+
Coord C1 exon
chr6:38842368-38842505
Coord A exon
chr6:38842506-38842662
Coord C2 exon
chr6:38842663-38842903
Length
157 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
TTTCTCTTTCTTTCTGAAAGATG
3' ss Score
7.77
Exon sequences
Seq C1 exon
AAAAGAACTCAACTTGCTGCAGAAGCTGTATGGATTGTATGACACCGTAATGAGCAGTATTAGTGGTTATTATGAAATACTTTGGGGAGATGTAGATATTGAAAAAATTAATGCAGAACTGCTGGAATTTCAAAACAG
Seq A exon
GTGAGTTTCAATGGAATTTTTTATAATGCCTGTCTTCTTAGGATCCTATAGGTATTTCAGAAGCTAATTTATTCCCTAATATAATAGTGTATATACATAAAACCTTCCTCAAATAAATGTGAAGGTGGCATATTTTTTTTCTCTTTCTTTCTGAAAG
Seq C2 exon
ATGTCGTAAACTTCCAAAAGGACTTAAAGATTGGCAAGCTTTTTTGGATCTCAAAAAGAGAATTGATGATTTCAGTGAGTCATGTCCTCTACTGGAAATGATGACCAATAAGGCCATGAAACAGAGACACTGGGATAGAATCTCCGAGTTAACTGGAACCCCATTTGATGTGGAATCTGATTCTTTTTGCCTTAGAAATATCATGGAAGCACCACTCCTTAAACATAAGGATGATATTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721:ENST00000359357:32
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:
PF083938=DHC_N2=FE(11.1=100)
A:
NA
C2:
PF083938=DHC_N2=FE(19.4=100)


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:
GCTGTATGGATTGTATGACACCGT
R:
CAGTGTCTCTGTTTCATGGCCT
Band lengths:
246-403
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