Special

HsaINT0050025 @ hg38

Intron Retention

Gene
Description
dynein axonemal heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]
Coordinates
chr6:38935592-38938226:+
Coord C1 exon
chr6:38935592-38935697
Coord A exon
chr6:38935698-38937973
Coord C2 exon
chr6:38937974-38938226
Length
2276 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTG
5' ss Score
7.76
3' ss Seq
TTTCCTGTTTTGAATTTCAGGCT
3' ss Score
9.68
Exon sequences
Seq C1 exon
GAGTTAGAGGCTGAGAGGGTTAAACTTTTGGAGGATGTTACTTTTAATAAGCGGAAGATGAAAGAACTTGAAGATAACCTCCTCTATAAATTAAGTGCTACAAAAG
Seq A exon
GTATTGTGTTATTAAGAAGTAATGAAATAACGGATTCTGAATAAGGATTTCATTTACACTCTTTTCAATGCCCTCATGACTATAGATGTTAGGAAATACTCATGTTATCAATGCAAAAACAAGCAAGGCAATTTCCATCTAGACATTAAAGAGGGACGGCAGAGAATCTGATTTTTGAATTAGCAAATAGAGACTGAGCATCTGAGAATAACACAATTTTCTTGATATAATTGCTTTCTCCTGAGAAAAATTAGGGCTCCTGATAGAGCTAGATAACTCATTATAGGTTAATTTGCTTGCCCCAAAGAAACTAATGTGCTCAATCTATTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCTCCCAAGCCAGACGTGGTGGCTCATGCTTCTAATCCCAGCACTTTGGGAGACCAAGGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGAACAGCCTGGCCAACATGGTGAAACTCAATCTATTTTTTTTCAAATTGACTCTTTCATTTGGCATTGAAATGCAGTTATTGCAACGGGTTATGACACATGTAATCCATGTCAGAAGAGCTTGGGTACCAAAGGCCCAGCTTACCCTCTACTTGGCTTGACCTCCCACTTTAGATGGGAAAGACAGGTTCTCCTCTGGGCAGCCAAATCATCATGCCACACCTCAATTTGAGGATGTACTCTCTCTGCAATATATAAAAAGAAAATTTTATCCAAAGAAAATAAAATCAACAAACATATTGTTCTGTAGCAGACAAATCACAGAAACCTGAATTCTACTACCTTATTAGAAGTGAATGAATACTTCACAACTGCACCTTAATCCCGGGATGTTATTTAAACAAGTCTGACCTTCCAGAAGTACTGTACCTTTATGGTGAGCTTAGTGAAAAGTCCTTTTATCTGCCTACTCGCACTGCTCCCGCTAGTGAAGTTGTCTGTTTCTTGGTCCAGTGACTCCTCCCAGCCATTTGGGATACCCCTGGGCATTAAAAATATAGCAAGCAGAGCTGAGGGCTGCTCCCCTAGTCTAGCCAAGAGTGTGCTGGATCAAGACCTCTCTCCTTGAGGTTAATCCCAATTTGGACTTCCACAGTAGACAGCATACCCGTTGGAGTAACACAGCCCTTCCTGCAGCACTTGTCTGCCATCCCGAACTCTAGGGTAGGCCAGAGTGCTGCTGTTCGCAGATATGGGAACTGTTCGCAGATATGGGGACTGTTAGCTCAGTACATCCAAGGTGTCTTTCCTTAGATTTTAATTAAAAACCAAATTCATTGTCATAAACATGCACTATTTCCATTAAAAACAATAATAAAAAAAAAGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAACTGGAAACCATCATTCTCAGCAAAGTAATATCAGAATAGAAAACCAAACACCGCATGTTCTCACTCATAAGTGGGAGTTGAACAATAAGAACACATGGACACAGGGAGGGGAACATCACACACTGGGGCCTGTCGGTGGGTAGGGGTCTGGGGGGAGGGATAGCGTTAGGAGAAATACCTAATGTAAATGACAAGTTGATGGGTGCAGCAAACAAACATGGCCCATGTATACCTATGTAACAAACCTGCACGTTCTGCATGTGTACCCCAGAACTTAAAGTATAATAAAAAAAAAAATAATGAAAGGCAAAACTAAAAATAAAATTCAAGTTTCTCTTCCTGGTGAGACATTTTCACTATACCCAATTTGCTCTTGTTAGAGACAGAGGGATTAGAGTTTTCTATAGCAACGACTGTTCTACTAAAGCAGTGTGAGGAGTGTACCATTCAACTATCAGCATGACAGTCAGCCCATGTGTGAAGTGTTCAGGTTAGCTACACCCTGAGACAAGCAGCGTGGACAAGCTGTGACACTTTGAGGAGAGCCACCAAGATGACAGTGGGTGTGAAGCCTATCACATGGGGAACAGCAAAGAGCACTGGAGACATGATCATTGTCTTGAGACATGTGAAGACCCAATCAAATGGGTCTTTTGCTTTTTGCAGATGTTTAGGCAGAGCAGGGGATAGTCTGTCAGCAGGAATGTTCAGAAGGCTTCAGGTATTGGGTGGTAGTTGGACTAGAAGCTTTTTGGTGTCTTAAGATTCTACTGTACCAGTAGTCTTCCTGACTTTGGAGACATCAAGTTGAAAGCTAACAGCGTTTTTTTTTTTTCAGAAGAGATGTATCTTGCTTTGCAAGTTTCCCGTCTTGTGTACTACGGTTTTCCTGTTTTGAATTTCAG
Seq C2 exon
GCTCATTGGTAGATGACGAATCTCTCATTGGTGTACTTCGAACTACCAAGCAGACAGCAGCTGAGGTAAGTGAAAAGTTGCATGTGGCTGCAGAAACTGAGATCAAGATCAACGCGGCTCAGGAGGAGTTCCGGCCCGCAGCCACCCGCGGAAGCATCCTCTACTTCCTCATCACAGAGATGAGCATGGTCAACATCATGTATCAGACGTCATTGGCCCAGTTCTTGAAGTTATTTGACCAGTCCATGGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721:ENST00000359357:75
Average complexity
IR
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:
PF127812=AAA_9=FE(15.2=100)
A:
NA
C2:
PF127812=AAA_9=PD(10.0=27.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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
  • Pre-implantation embryo development