Special

HsaINT0049996 @ hg19

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:2952]
Coordinates
chr6:38840682-38841152:+
Coord C1 exon
chr6:38840682-38840923
Coord A exon
chr6:38840924-38841011
Coord C2 exon
chr6:38841012-38841152
Length
88 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGG
5' ss Score
6.92
3' ss Seq
ATTCTGTTTCTTTGTTGCAGGCA
3' ss Score
10.6
Exon sequences
Seq C1 exon
GTGAAAACATTTTCCTCATTTTAGATGGTCCTGTGGATGCCATCTGGATTGAGAACTTAAATTCCGTTTTGGATGACAATAAAACTCTGACGTTAGCTAATGGAGATCGCATTCCCATGGCCCCTAGTTGTAAGCTTCTGTTTGAAGTCCACAATATCGAGAACGCCTCTCCTGCCACGGTTTCTAGGATGGGCATGGTCTATATCAGCAGCTCTGCTCTCAGCTGGAGGCCAATCTTACAG
Seq A exon
GTGGGGCAGAGAGATGGGAAGAAGAACCCTCAGAGTCTCTCCACGTTTCACTTTCTCAATAAACACAGATTCTGTTTCTTTGTTGCAG
Seq C2 exon
GCATGGTTGAAGAAACGCACTGCACAGGAAGCTGCTGTATTCCTGACACTGTATGAGAAAGTCTTTGAAGATACATACACATATATGAAGCTAAATCTCAATCCCAAAATGCAGCTCTTGGAGTGCAACTATATTGTGCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721-DNAH8:NM_001371:49
Average complexity
IR-S
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:
PF077289=AAA_5=PD(46.0=77.8)
A:
NA
C2:
NO


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:
ATTCCCATGGCCCCTAGTTGT
R:
ATACAGCAGCTTCCTGTGCAG
Band lengths:
172-260
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