Special

HsaINT0049149 @ hg19

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 1 [Source:HGNC Symbol;Acc:2940]
Coordinates
chr3:52387396-52389071:+
Coord C1 exon
chr3:52387396-52387649
Coord A exon
chr3:52387650-52388858
Coord C2 exon
chr3:52388859-52389071
Length
1209 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
3' ss Seq
TGGCTTGTCCCCGACCCCAGGCA
3' ss Score
6.84
Exon sequences
Seq C1 exon
CCTGCCAGGAAGTGGCCTTGGACATCCGGGCCCGCATCGAGGAGTTCAAACCATACATCCCACTGATCCAGGGGCTGCGCAACCCTGGCATGCGGATCCGGCACTGGGAGACACTGTCCAACCAGATCAACATCAATGTCAGGCCCAAGGCCAACCTGACCTTTGCTCGCTGCCTGGAGATGAACCTGCAGGACCATATCGAGAGCATCAGCAAGGTGGCTGAGGTGGCTGGCAAGGAGTACGCCATCGAGCAG
Seq A exon
GTGGGTAGCCACCAGCGGGCCCAGCCACTCCAGCCAGGCCCTGCCGGACAGCCTGACCTCCTGCTCTGGCAACCACAGCCACTTGGGAGGATGACAGTAATAAGCCCCATCCCTGGGGTCATGAGGCCCAGGGGTTGAGATGCATTCTATTAAGTGAGTTAATAATGCACATAAAATTCTTGACAGTGTCCACCATTGCTATTATTTTTCAGTTACTCCTCTCAAGAGCCCCAGGAAGGAGCTAATAGCATTAGCCTCAATTTAACAGATGTGTCAGGCCGGGTGCAGTGACACATGCCTGTAAATCCCAGCACTTTGGGAGGATGAGGAGGAAGGATCGCTTGAGCCCAGGAGTTTGAGACCAGTCTGGGCAACATAGGGAGACCCCCATCTCTACAAAAAATTAAGATATTAGCCAGGCATGGTGGCACATGCTTGTGGTCCCAGCTTCTTGGGAGGCTGAGGCTGCAGTGAGCGGTGATTATGCCACTGCACTCCAGCCAGGGAGACAGACTGAGACCCTGTCTCAAAACAAAACAAAAGAAAACAAACAAACAAAAAAACAGATAAATCAATTAAGGCTCAGAAGGGTTCAGCAACTGGCCAGGATGACACAGTAAATGCCAGAGGTGAGACCAGCGCCCACACTCCTCCTAACCTTAGCTGCCTCCCAACATGTGCGTACAACCACATGCAGCACATGTGTAACAGTGAACTGGGCTGAACACAGTGGCTCACGCCTGTAATCCCAGCACTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATAGTGGGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAATCTGGGAGGCAGAGATTGCAGTGAACCAAGATTGTGCCACTGCACTCCAGCCTGGGCTACAGAGCGAGACTCCACCTCAGAAAAAAAAAAAAAAAAGAGTGAATTGGCCCTGAATTCAGATGAGGGGCTCACACGGGACTTGTTGCCAGACAAGCCGAGAGTATTTGCCAGAGCGGCCATGTGGAGGTCATGGCCAGGTACTGTCTGCTGCTTCCCTGGGCAGGGCTGGTCAGACAGCATCAGGACCAGCCCCTCCCAGGACTCAGCCTGGCTTGTCCCCGACCCCAG
Seq C2 exon
GCACTGGACAAGATGGAGAAGGAGTGGTCGACCATCCTGTTCAATGTACTGCCCTACAAGGCGACAGACACCTACATCCTGAAGAGCCCGGACGAGGCCTCACAGCTGCTGGACGACCACATCGTCATGACCCAGAATATGTCATTTTCACCCTACAAGAAGCCCTTTGAGCAGCGCATCAACTCCTGGGAGAACAAACTGAAGCTGACCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114841-DNAH1:NM_015512:20
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.016 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF083938=DHC_N2=FE(20.4=100)
A:
NA
C2:
PF083938=DHC_N2=FE(17.0=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:
CGCATCGAGGAGTTCAAACCA
R:
TCTGGGTCATGACGATGTGGT
Band lengths:
358-1567
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