Special

HsaEX6042678 @ hg38

Exon Skipping

Gene
Description
dynein axonemal heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:2949]
Coordinates
chr16:20959179-20969990:-
Coord C1 exon
chr16:20969792-20969990
Coord A exon
chr16:20963284-20965425
Coord C2 exon
chr16:20959179-20959404
Length
2142 bp
Sequences
Splice sites
3' ss Seq
CTGTTTCTTGTTCCAAATAGGTA
3' ss Score
10.56
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
Exon sequences
Seq C1 exon
AACGAATGTGAGGGGGACCTAGCTGAGGCAATGCCTGCACTCGAGGCTGCACTAGCTGCTCTGGACACCCTGAACCCGGCCGACATCTCGCTGGTGAAGTCGATGCAGAACCCACCAGGCCCTGTCAAACTGGTCATGGAGAGCATCTGCATCATGAAAGGGATGAAGCCAGAGAGGAAGCCAGACCCCAGTGGCTCCG
Seq A exon
GTAAGATGATAGAAGATTACTGGGGGGTATCCAAAAAGATTCTTGGGGATCTGAAATTCTTGGAGAGTCTTAAGACATATGACAAAGACAACATCCCCCCACTGACCATGAAGCGGATCCGGGAAAGGTTTATCAATCACCCGGAATTCCAGCCAGCTGTCATTAAAAATGTATCGTCGGCCTGCGAGGGTCTGTGCAAGTGGGTGAGGGCCATGGAGGTGTACGATCGCGTGGCCAAGGTGGTGGCTCCCAAACGGGAGCGACTGAGGGAGGCAGAGGGGAAGCTGGCTGCACAGATGCAGAAGCTGAACCAGAAAAGAGCAGAGCTGAAGCTGGTGGTAGATCGGCTCCAGGCCCTGAATGACGACTTTGAAGAGATGAACACCAAGAAAAAGGACTTGGAGGAAAACATTGAAATCTGCTCCCAAAAGCTGGTCAGGGCAGAGAAACTGATCAGTGGTCTTGGGGGAGAGAAGGACAGATGGACCGAAGCTGCCCGACAGCTGGGGATCCGCTATACTAATCTGACTGGTGACGTGTTGCTGTCCTCAGGAACTGTGGCTTACCTGGGCGCTTTTACAGTGGATTATCGGGTCCAGTGCCAAAATCAGTGGTTGGCTGAATGTAAGGACAAGGTCATCCCTGGCTTCAGTGACTTCAGTCTCAGCCACACGTTAGGGGATCCCATAAAAATCCGTGCCTGGCAGATTGCTGGGCTTCCCGTTGACTCCTTCTCCATCGACAATGGCATCATTGTATCCAATTCCAGACGCTGGGCCTTAATGATTGACCCTCACGGGCAGGCCAATAAATGGATTAAGAACATGGAGAAGGCGAATAAACTGGCTGTCATCAAGTTCTCTGATAGCAACTACATGAGGATGCTGGAAAACGCGCTGCAGTTAGGCACCCCTGTCTTGATTGAAAACATTGGAGAAGAGCTGGATGCTTCTATCGAACCTATCTTGCTCAAGGCAACATTCAAACAGCAAGGAGTTGAGTACATGAGGCTGGGTGAAAACATCATTGAATATTCCAGGGATTTTAAGTTATACATCACAACCCGTTTGAGGAATCCACATTACCTCCCAGAAGTTGCCGTGAAGGTCTGTCTCCTCAACTTCATGATCACCCCCTTGGGTCTCCAAGATCAACTCCTTGGCATCGTGGCTGCGAAGGAGAAGCCAGAGCTGGAAGAGAAAAAGAACCAGTTGATTGTGGAAAGTGCCAAGAACAAGAAGCATCTCAAGGAAATTGAAGATAAGATCTTGGAGGTTCTCTCCATGTCCAAGGGTAACATCCTGGAGGATGAAACCGCCATCAAAGTTCTGTCCTCCTCCAAAGTGCTATCTGAAGAGATCTCAGAGAAACAGAAAGTTGCTTCCATGACAGAAACGCAGATTGACGAGACTCGGATGGGCTACAAGCCAGTGGCTGTGCATTCTGCCACCATCTTCTTTTGTATCTCGGACCTGGCCAACATCGAGCCGATGTACCAGTACTCCCTGACTTGGTTCATAAATCTCTACATGCATTCCTTGACCCACAGCACGAAGAGCGAGGAACTGAATCTGCGCATCAAGTACATCATTGACCATTTCACCCTGAGCATCTACAACAACGTGTGCCGTTCTCTGTTTGAGAAGGACAAGCTACTCTTCTCTCTCCTCCTGACCATCGGCATCATGAAACAGAAGAAGGAAATTACGGAGGAGGTGTGGTACTTCCTTCTCACTGGAGGCATCGCACTGGATAACCCCTACCCCAATCCAGCTCCCCAATGGCTGTCTGAGAAGGCATGGGCAGAGATTGTCCGTGCATCTGCCTTACCCAAACTGCATGGCCTGATGGAGCATTTGGAACAGAACCTGGGTGAATGGAAGCTGATCTATGACTCGGCCTGGCCCCATGAGGAGCAACTCCCTGGGTCTTGGAAGTTCTCTCAAGGATTGGAGAAGATGGTGATCCTTCGATGTTTGCGGCCTGACAAAATGGTGCCAGCGGTCCGGGAGTTCATTGCTGAACATATGGGAAAGCTGTATATCGAAGCCCCTACGTTCGATCTCCAGGGATCCTACAATGATTCCAGCTGCTGTGCGCCTTTGATTTTTGTGTTGTCTCCAAGTGCAGACCCAATGGCAG
Seq C2 exon
GCCTGCTGAAGTTTGCTGATGATCTTGGTATGGGAGGTACCAGAACACAGACCATCTCCCTTGGCCAAGGCCAAGGCCCTATTGCTGCCAAAATGATCAACAATGCCATCAAAGACGGGACCTGGGTGGTCTTACAGAACTGCCACCTGGCCGCAAGCTGGATGCCTACCCTGGAGAAGATTTGTGAGGAGGTGATTGTTCCTGAGAGCACCAATGCCAGATTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000158486-'82-96,'82-88,84-96=AN
Average complexity
A_C3
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.224 A=0.004 C2=0.026
Domain overlap (PFAM):

C1:
PF127772=MT=FE(18.8=100)
A:
PF127772=MT=PD(59.0=29.0),PF127812=AAA_9=WD(100=32.3),PF0302810=Dynein_heavy=PU(18.4=18.3)
C2:
PF0302810=Dynein_heavy=FE(10.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains