Special

HsaINT0049358 @ hg19

Intron Retention

Gene
ENSG00000105877 | DNAH11
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Coordinates
chr7:21904153-21906281:+
Coord C1 exon
chr7:21904153-21904275
Coord A exon
chr7:21904276-21906087
Coord C2 exon
chr7:21906088-21906281
Length
1812 bp
Sequences
Splice sites
5' ss Seq
AAGGTATGT
5' ss Score
9.79
3' ss Seq
GTTTCCCTATCATATTACAGGCA
3' ss Score
7.98
Exon sequences
Seq C1 exon
ATTTTGTTGAGAAAGAAAGAGATAGACCCTCTTGAATTGGATTTCCTGCTTCGATTCACAGTTGAACACACTCATCTGAGTCCCGTTGACTTCCTAACTTCTCAGTCATGGAGTGCTATCAAG
Seq A exon
GTATGTTAGGAATACAGTTTCTCAAATTCTGGATCTTATTTAAAATATTAGCTCTCTCCAGTGTTGAAATGTAAACATTAAAGAATACAGGTGATGTATTAAGCACCATTTCAGTTGTAGAAATGCACTGTATAATGTGATGTTATTAATCTTTGTATTATTCAATTGGTTAATTTCTCATTTAGATGTAAAGGAGCTTTTGGCTTATGTATGCGTGGAAAAGTTAATAAATATGTACAATCTGTCAGGACCTTTGATAAAAGCCAAGTGATACAAATGAATATTTTTAAAAAGTTCCTTAAATCTAAAATTTGTTTTCTTTTTAAATTTCCTTAAAAATTTGTTTTCTTTTTAAATCGTTTCACCATTTTTCTAAATAGTTCTTTAAATTACACCACAGTGGAGTCGTTTATTCTCATTGTAAAATGTTTAAGAAAAACAGAATATTTTAGAGAAATAAGTGACAGTTGCCTTAAACCTCAATTATCAATCCTCATTGCATTTTTCTGTCAAAGGCCCTATTGTTAGAAGTTAATTCTTCCAGGATCTGGAGTATCTTAATGATGTTCAACATATGCTAAGCTTTGCCCTACTCTTTTTTCTAAGAAGGAAACATTTCTGTGCATTGGAAATAACTGTTACCTCTTATTTTTATATATGTTCAGCTTTTTAAAGTAGTATTTGTAATTAGATTGTAACTTTAGAATTCAAAATTCAAATTCAAATGTGTATCAGTCAGGGTCTTAACAGGAAACAGATGGCACATTCAAAAGGTTGATGAAGAAAGTTTAACCAAGAGTCTGTTTTCATAGTATGGGCAAGAAGGATTAGGAAATCAACCAGGGGATGGGGAAGGAAAAAGGAGGAAAAGGACAGTTACTGGAACTTCATAAGAAATGAAGTTATGGGAGAGAGCCAACCTTAGAGGATCTGTGGCCTGTGGCAGAGAAACATAGTCCCTCCCAAACCACATTCCCACGAGAAAGAGCTGGGGTAGAAATGTTTCCAGAAAGGGGTCCTGATCCAGACCCCAAGAGAGGTTCTTGGATCTCGTGCAAGAAAGAATTCAGCGTGAGTCTGTAAAGCGAAAGCAAGTTTATTAATAAAGGAATAAAGAATGGCTACTCCATAGGGAGAGTAGCCCTGAGGGCTGCTGGTTGCCCATTTTTATGGTTATTTCTTGTTGATATGCTAAACAAGGGGTGGATTATTCATATCTCCCCTTTTTAGACTTTATAGGGTAACTTCCTGACGTTACCATGGCATTTGTAAACTGTATGGCACTGGTGCAGTGTAGCAGTGAGGACAACCAGAGGTCACCCTCATCACCATCGTGGTTTTGTTGGGTTTTAGCCAACTTCCTTACTGCAAGCTGTTTTATCTTTATGACCTGTATCTTGTGCCAACTTCCTATCTCATCCTGTGACTTAGAATGCCTTAACCTCCTAGGAATGCAGCCCAGCAAGTCTCAGCCTCAATTTACCCAGCTCCTATTCAAGATGGAGTTGCTGTGGTTCAAACGCCTCTGACAGAAGTACCCCCACCTCTCTCTTCTCCAGTCTTCCAGGCTCCTGCCATTGCTTTCTGTTGGCCAAACCCAACTAGGTCAGGGAACCAGGGAACTCAGCTCAAGTGTCCTTTGAGCTTACCCTCTCAGCAGAGCAAAAAAAAAAAAAAAGGAAATCTGAAGAGGAGAGTGAATACTATCCAGCACAGTTTTTTTACATAAGATTAGATACATTCACAAGTCTTCTTCTCAAACTGTAAAGTATCGTTCACACCATTCCTACTTGTTTCCCTATCATATTACAG
Seq C2 exon
GCAATTGCCGTCATGGAAGAATTTCGAGGCATAGACCGAGATGTGGAAGGATCTGCCAAGCAGTGGAGGAAGTGGGTAGAATCCGAGTGTCCAGAAAAAGAAAAATTACCTCAAGAATGGAAGAAGAAAAGTTTAATACAGAAGCTGATTCTTCTGAGAGCAATGCGCCCTGACAGAATGACGTATGCTCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877-DNAH11:NM_003777:70
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:
PF0302810=Dynein_heavy=PU(2.8=48.8)
A:
NA
C2:
PF0302810=Dynein_heavy=FE(9.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTGTTGAGAAAGAAAGAGATAGACCC
R:
GAGCATACGTCATTCTGTCAGGG
Band lengths:
310-2122
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development