Special

HsaINT0049250 @ hg38

Intron Retention

Gene
ENSG00000197653 | DNAH10
Description
dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr12:123867903-123870485:+
Coord C1 exon
chr12:123867903-123868119
Coord A exon
chr12:123868120-123870365
Coord C2 exon
chr12:123870366-123870485
Length
2246 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGA
5' ss Score
6.71
3' ss Seq
TCAACCATGATTTCCTGCAGGTC
3' ss Score
8.33
Exon sequences
Seq C1 exon
GTAACCCAGTTAGCCAAGATGTTGGATGCGTTGCTAGAAGGAGAAATAGAAGACCTTGACCTGCTGGAGTGCTACTTCCTGGAGGCTTTGTACTGCTCTCTGGGAGCCTCCCTGCTTGAGGATGGAAGGATGAAATTTGACGAATATATCAAACGCCTTGCTTCTTTGTCTACTGTTGACACAGAAGGAGTTTGGGCCAACCCTGGGGAACTGCCAG
Seq A exon
GTGGGAACCGAGTGTCGCCTGTTTCCCTGCTCTGAGTGCCTTTGGTTAAATTTCTAGAGGAAGTGAATGAGCTTTTCCATATTTCTGTCTGTATGAGTTTTCCAGATTGTTTGCTTCTTTAGAGAAACATGCAATGGTCAGAGCACATGGCGGAACACCCAGGAGCGGTTCACATGCATTGACTGCTGTGACAGAAGCCCAGGCCCTCTGGGTGGTCTTTCTGGATGAGAGTCAACTTCTCTTGCCTCAGCTTAGGCACTTGCTTCCTTTGCTCTTTAAACTTTTCACATTCTGCATGACTTTGAGTTTCTTCTTCTGTGGGCTTCCCTATCTGTCTTTTTAATTTTTATTTTTAACCATCTATCTCCATTTTCACCATATCATTCATCTGCTGTATTCCTGAGTATTTGCACAGTAGACAATCAAGTGTGGATTTGTAAATCGTTCATAGGAAATCATACAATTAACATTTTATGTTTTTGCACAAAAATGTGCATCTTCAATGAATCATACATGATGAAAAAGATGCATTCTCCAAGGTCTATATGCAATGGTAGGACCCTTCTTTATCCATCTCTTATTGCTATTCGAGCATGGCTTGGAATGTAGATGGCTTTTGAAGTTGTATTTTATACTCCTTACCTGGTGGTCTTTTTAAAGTTTAAAATGAAATGGCCTCCGGTCTTTCTAATGGACAGTCATGGAGCAAATCAAAGATGTTTTTCAGGTCCCTGCTTTATTCGGTGGGAGTCTGAGTGCACTTTTCCAGAACTGAAATCTCCCTTTGGGGAGTGCTTTTCAGCTCCGCCAGCCACGCTGGCTGTGCGTTGCTGCCATCTGCAATTCCCTCACTCGGAGACAATGTTGGCCTGCTTCCCTGGCTTGTCTCCCTCATTTGCCCTCATCTTGGGGGCCTGAATGGCCCTGTGGGCATCCCATTTCCAGACACCTGCTCACAGCTTCAGCCCTGCAGGCCCTCGAGCATACGCTTGACGGTGATCTCTGGCACTGTCATGTCTGCATCACAAATCCTGCTCTCCACCTACTCTGCCTCTGAGACTCGGGCCACATGTGTTTCTGTTTGGCCTCATGGGGATGGACACTGTGTCGCCCCAGTGTCTGCTGTTGCCTCGAGCACCCATACTTGCCCCTTCCCTGCATCCTCACTTCCTTGGCTGGTGGCCTTCACTTCAGCCACTCTTGCCTGAGACCTCCGCATGCCTTGCCTAATTGCTCTGCTGAATCCCTCCGAGAAAACTCCAAGTCTGTCTTCTCTGCCTGTCTAAGGGCTGACAGGGAGAAGACCATGCAGCCACAAAGACAGATGTCTCCATAAATCCCAGTCCCCAGCTGGCACACTCACTCCTGGCTCCAAAGGAGCATTGGGCCTTTTCCCCAAATATCTACCCTGCCCTTTCCGCGCTCTCCGCAGCTGATCTTTCTCCCTGCTTCAACAGGAACAACGGAAGCTGTCTGATAGGAATCTCTCCTTCCAGCTGAAAAGCCTATAGCTCCTGTCTCTGACTTTCTCCTTTTACAGTGGAAGAGGCCACCCCCACTGCACCCCAGCCAAGGCCAACCCAGCCCCTTCCTCCTTCTCAGGCTCCTCGCTCCATCTGAGTTTATCTCTCTCTCTCATGTTCAGTCTCCGCCTCTCTACCATCCTGTCAGCTCTTAGACATGCTCAAGTAAAGCCTTGCATGGCCTGAGCGGAGGCGATGGTGATTACTCGGGCACCTGCAGCTTCCATCTCTCCCCTGCCCCGCCTGGGTTGCTGCCTTCCCGCATTGTCCGTTGTTCCTGCCCCTCTCCTGCTGCAGCACTTATGGCTCCACACTGAAATGGCCACTTCTTGCCTGTATCTGTCCCCCACCTGGCCCTCGAACAACTGCAAGGGTAGGGACCAGGGCTCTCTGCTTCACTGTTGTATTCCCAGGGAAGTGTATGTCCAGTGAAAGGGAAGTGTTAGTTGAAAATACTCAGAAAGTGCCTGACAAGTGCACAAGTCACATTAGTGACTGTCCCGTGAACTAGAAGCATAAGCTCCAAATACTTGGCATCTGTCCAGTGATGAGTAGCATTAGTTCAAGGTACTCGGTATCTGTCCAGTGAAGGAGCAGCATTGAAGTACTCACTATGGCCTCCGTGCAGTACAAGCAACATTAGTTCATTTCAAGCATGTGCCAGAACTGCTTTTGTATTTCCGTGTTTATGATTCAAGTGAAATCAACCATGATTTCCTGCAG
Seq C2 exon
GTCAACTTCCAACCTTGTATGACTTTCATTTTGATAACAAACGGAATCAATGGGTCCCATGGAGTAAATTAGTTCCAGAGTATATTCATGCCCCCGAGAGGAAATTCATCAACATCCTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653:ENST00000409039:42
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:
NO
A:
NA
C2:
PF127752=AAA_7=PU(4.8=31.7)


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