Special

HsaINT0049156 @ hg19

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 1 [Source:HGNC Symbol;Acc:2940]
Coordinates
chr3:52393932-52394440:+
Coord C1 exon
chr3:52393932-52394095
Coord A exon
chr3:52394096-52394326
Coord C2 exon
chr3:52394327-52394440
Length
231 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGG
5' ss Score
8.41
3' ss Seq
TCATCTCCCTGCACCGCCAGGTA
3' ss Score
8.02
Exon sequences
Seq C1 exon
CTCAGTGATCTGGTGGCCCTTGTGCGGGGGAAGCTGTCCCGCATGCAGCGGGCAGTGCTGTCAGCGCTAATCGTCATTGAGGTCCATGCCAAGGACGTGGTGAGCAAGCTAATCCAGGAGAACGTGGTCAGCGTGAATGACTTCCAGTGGATCTCACAGCTGAG
Seq A exon
GTGAGGACATGGGGGGCGCCCCCAGGGCCAGAGCAGCTGCCAGGAAGGGGCAGGGGAAAAGAGAAAAGTCAGTTAGCAATAAGCTGGTCTCTGTCCTTGAGGTTCTGGGACAAGCTGGGTATGGGTACCTTAATGCCCTCATTCCCAAAAAGAACCCTCTCTCCTTGACTATATACCCTGCCCAGTGGCCCATTGCCCCATGGCCAGGCCCTCATCTCCCTGCACCGCCAG
Seq C2 exon
GTACTACTGGACAAATAATGACCTGTATATCCGTGCTGTGAATGCTGAGTTCATCTATGGCTATGAGTACCTGGGCAACAGTGGGAGGCTGGTGATCACGCCCCTCACCGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114841-DNAH1:NM_015512:27
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:
NO
A:
NA
C2:
PF127742=AAA_6=PU(8.2=48.7)


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:
CTCAGTGATCTGGTGGCCCTT
R:
GTCGGTGAGGGGCGTGATC
Band lengths:
276-507
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