Special

HsaINT1011302 @ hg38

Intron Retention

Gene
ENSG00000197653 | DNAH10
Description
dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr12:123845971-123848095:+
Coord C1 exon
chr12:123845971-123846154
Coord A exon
chr12:123846155-123847960
Coord C2 exon
chr12:123847961-123848095
Length
1806 bp
Sequences
Splice sites
5' ss Seq
CAGGTGACT
5' ss Score
6.6
3' ss Seq
TTGCATTTGGCTTATAACAGGCG
3' ss Score
5.43
Exon sequences
Seq C1 exon
TATCCTGGAGGCCCGAGAGTTTGACTGGGAAAGTCAGTTGCGGTTTTATTGGGACCGGGAGCCGGATGAGCTGAACATCCGCCAGTGCACGGGAACCTTTGGCTACGGCTACGAGTACATGGGCCTGAACGGCAGGCTGGTCATCACGCCCCTCACCGATCGGATTTACCTGACGCTCACCCAG
Seq A exon
GTGACTGCCAGCCTGGCACTTGTGGTTACCACTTACCTTGGGGCGGGGCATTTTCTCTAAGCTTGAGGTGTGATGACTGCAGTGATTGAAATAGCAGGGGAGATCATTGCTTTGAAATCTCGAAAAGCTTTTCCATTTGGGATGTGACCAGATTGTCACCATTTGGGATTGGCATGTAAGTGTGGCCGTGCTTAGCCACTGGTACACTGGTCCCTAGGTAATGGTGTGTCAGGGGTATTGGTAGAGGCCAATGCGAAAATGCAGGAATGTCAAAGGTGGTGACTGTTAGGGCAAGTGTGATGTGGTTTTGCACGTCTTGTGACAGCTTTTATTCCAGAATATATCCGTTCAAGTGAACGGCCTTGGATGATAGAGATAGTGTCTCCCTCCAGGACAGAGGGTAAACTTGTTTGTTGTACAGGAAATGAAGATAACACTTCCATCCAGGCAGAGCTTGGGAAGGTTTGCAAGCAACCCCCAAGACTGTTTGTCAGATGCTTGCTAGTTTTCTTTTTTTAAATTAGAGATGAGGTCTTGATATGTTGCCCAGGCTTGCCTTGAACTCCTGGCCTCAAGTGATCCTCCCACCTTGGCCTCCTGAGTAGCTAGGACTATAGCATTCACTGCTGCACCTGGCTACATTGGTGGTCTCTTAGGCTCACAGTTTCTCAGCTGTGACTCATACCCACTGTGGATGTGGCATGCACCTGGGCCCGTCTCCACATCACACCATGGGATTTGGGGGGACAAGGATAAAGGGAATGAGTGAGAACAGGAAGCCCCTGCTGCCTCCTGTGCTGTGAGTGATAAAGTCCTTTGTTTTTGAGAAAAAGAGTGTCATCTTATCTGTATTGGTTAGGGTTCCACAGAGAAATAGAACCAATAGGACATAGCTAGCTAGCTGGATGGCTGTCTGTCTGTCTGTGTATCTATCTATCTATCTAATCTATCTATCTTATCCATCCATCCGTGCATCCATCCATCTACATATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATGTATCTATCCATCCATCCATCCTATTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCTGTCTATTTATCATCTCGATCATCTATTTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGGATATTTAGGAGGAGATTTATTATGAGGTATTGACTCATGTGATGATAGGGTCTGATTACTCTCACAATCTGCCATCTGCAAGCTGGAGGACCAGGAAGGCCAGTAGCATTTGAAGTTCTGACAGTGAGAGAGCCAATAGTGTAGACTCGTGTCTGGGTCTGAGGGCCTGAGAACCCGAAGTGCCAAGGGTAGAAGCCCAGTGCCCTGGCTCAGTCAGTCAGGCAGCACCAGTGTAACCTCCCTCCATCCTTCTGTTCTGTTCAGTCTTCAATGGATTAGATGATCAGGCAGCACCAATGTAACCTCCCTCCATCCTTCTGTTCTGTTCAGTCTTTAATGGATTAGATGAGGCCCACCCACTTTGGGGAGGGTCATCTGCTTTTCTCAAATGCTAATCTCTTCCTGAAACACACTCATGGACACTCCCAGAAATAATGTTTAGCCAGCTACCTGGGCATCCTGTGGCCCAGTCAAGTTGACACATGAAAGCAAACACCACATTCTTTCTCTATTCTGCACCTATAGTCACAGTGATGAATTTGGAAATGACACCCACTTCCTTCTGTGCACCAGAAAACATATGTTTTGCATTTGGCTTATAACAG
Seq C2 exon
GCGCTGTCCATGTATCTAGGTGGGGCCCCCGCCGGCCCAGCAGGAACCGGCAAAACCGAGACCACCAAGGACCTGGCGAAAGCCTTGGGCTTGCTCTGTGTTGTCACCAACTGTGGCGAAGGCATGGATTACAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653:ENST00000409039:31
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=0.111
Domain overlap (PFAM):

C1:
PF127742=AAA_6=PU(11.3=41.9)
A:
NA
C2:
PF127742=AAA_6=FE(19.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TATCCTGGAGGCCCGAGAGTT
R:
CTGTAATCCATGCCTTCGCCA
Band lengths:
318-2124
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains