Special

HsaINT0049262 @ hg38

Intron Retention

Gene
ENSG00000197653 | DNAH10
Description
dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr12:123894643-123897967:+
Coord C1 exon
chr12:123894643-123894723
Coord A exon
chr12:123894724-123897769
Coord C2 exon
chr12:123897770-123897967
Length
3046 bp
Sequences
Splice sites
5' ss Seq
TAGGTAAGT
5' ss Score
9.66
3' ss Seq
TTTTATTCCTTCCTCTTCAGGGT
3' ss Score
11.3
Exon sequences
Seq C1 exon
GTATGGTAAATAACACTGGTATTGACTGGTTCATGCCCTGGCCTCCCCAAGCCCTCCATGCGGTCGCAAAGTCCTTTCTAG
Seq A exon
GTAAGTCACAGCTGTTATGGGAACTGCATTATTGATAAAACAAAGCAATTTATTTTCCCTTTTCTGACTTTGAATTCTGGTCTTGTAGATTTCTTCACTGGAAAACCCTATGGTAACAAATGGCTTTCAATTTTGTTAGTATGTTTTTGGTTTATATTTGGTGTTTTAGTCCAAAGACATTTCAGGAGACTTAGCAAGGACAATTTAGGATAAAAATTGATTAGGTGTTCTCCACAGCAGCAGTTGGCAAAACCATGGTCTGCTGTCTAGTTGGCCCCTTACTTGTTTTAGTAAATAAAGTTTTATTGGTACACAGACTCACTCATTAATTAACATATTGTCTCTGGCTGCTTTTATGCTACAACCGCAAAGCTGAATAATTGCAACAGAGACCGTATGAGTACTGTTCGGCTCTTTGTAGAAAACATGTGCTGGCCTCTATCCAAAGAATGCTCCAAGGACAATTCAGCAAACATTCTGCATTCTCATTGAATTTCTAGCGTTTCAAACACCTAAGGCCTTGGATATTAATTTTAATGTTTGAATAAGAAAGGAAGTCTGTCTTCAGGGAACATCTTTTTCTTTTGACCTAACTTGAGCAGATTTATGATGAATGACACTGGGTAACCTTGAAAATAGTTTCAACCTTCTAAATCTGTACTCAATAATAAATAAATAAATGTTCCTATATGTAAGAAGAAATCATAACTTTAATCATAATGCAGTTTTGGGGGAAAAGGGGCCAAGAGAATGACTCTTTTCTGATGATATATCTCAGGTCCAGATGGTAAATATTTACAGCTTTTTCGCAACTACTCAATTCTGCCATTTTATCATGAAAGCAGTCATAGACAATACGTAAATGAATCGCTATGGCTGTGATCCAATAACACTTTATTTACAAAAACAGGGGGCGGGCTGGATTTGTCCTTTGGCCCGTAGTTGGCCAGCCCCAATATAGATGTCCCCTTGTTCTCAGAGGCGTATTTGCCGTTTCCATGTGTGAAGTGCTTGTGTTTGCTTTCAGTATTCAGTGATTCAGCATCATAAATAATGCTGCCTAGAATTTGCTTAGAACTTTTTTGTCCTTAGAATATACTCCCTGGAGGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAAAATGGTGAAACCCTGTATTTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGCCATGAGAATTGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCGAGTTTGTGCCACTGCTCTCCATCCTGGGAGGCACAGTGAGACTTTATCTCACACACACACACACACACACACACACACACACACACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAATATATTCCCTGGAATTGAGATGACTATGCCCAAAGGCACAGATATTTGTGAGGCACCGTTTTTCCTGCACACTGTAAAATGGGCCCTGGGGCTGTGTTTTGCTAACCCCGGAGTAACTCAGGACCAGCTCTGCAGAATCTGGATTAATCGGTACTTTCAATCTGTCTTTCCTTCCTCCATTTTAATATGAGACATTCTCTGCTTTGAGCTGAATGCATTTAACAACCTATCAGATAATCCAGGTGATGTGATCTTGACACTGGAAGCCATCATTCATTCTTTCAGCGGGTGTATAGGAAGGCCCACCTTTGCCGATATGTGCTGGGTGTCATCCAGCGGTGGGTAACCGAATAAGCCCACCCAGTCCTCGGGCGGGCGAGGGGAGCAACAGGGCAGAGTTAGACGTGGTGATCGCTTCTGAAAACCCAAGGCCCTTCTGCCACGGTGTCTTGGCCTTTAGGGAAGACAGGGCTTCCTAACAGTAGGGAAGGAATTAGGTAACAGAGTGAGACCCTGTCTCAAGAAAAAAAAAAAAAAAAAAGAAGGATTAGCACGGATCACTGCTGTGGCCCTGAAAAGCCACCAATAAGTGATAGCCATTCTTTTCTTGTCCTATTAAAAACTTTAACATCATTTTTTTATTGTAGTAAAATATATGTAACATAACATTTTCCATTTTAAGCATTTTGAAATGTACATGTGGCACTAATCACATTCGTAATGTTGTGAAACCAACACCACTGTCTGTTGCCAAAACTTTTCATCATCCCAAACTGAAACTCCATACCCGTTAAACACGAACTCCCCATCGCCCCTCCCTCCAGCCCCTGGCAACCTCGAATCTGTGTTCTGTCTGTATGAATTTGCCTGTTCTAGAGAGGGTTCGTATAAGTGGAATCATGCAATGTTTGTCCTTTGGTGTCTGGCGTCTTTCACTTAGCATCATGTTTTTGAGGCTCATCCGTGTTTCAGCATCGGAACTTCATTCCTTTTTACAAGTGAATACTATCCCCGGTATAGATAGGACACATTTTGTTCATCCATTCCTCCGTTGCTGGACGCTTGGGTCTTTCCACCTTTTGCTTATTGTGATAGTCTACAGTAAACATTGGCATACAAGAATTCATTTGAGTCCCTGCTTTTCAGTTCTTTGGGGTATATACCTAGGAGTGGAATTGTTGAGTCATATAATAGTTCTATATTTAACTCTTTGAAGAATCCCTGTTTTCCTTTCTTAACAAGCATGGCTGGGTGCGGTGAGTCACGCCTGTAATCCCAGCACTTTGTGGGGCTGAGGTGGACCGATTGCCTTAGCTCAGGAGTTAAGACCAGCCTGGGCAACATGGGTGAAACCTCACCTCTACAAAATAATACAAAAAATTACCCAGGCATGGTGGCCCATCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACCTGTGCCCAGGAGATGGAGGCTGCAGTGAGCCATGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACCCTGTGTCGAAAAAGAAAAAGAAAGAAAACATTTTTTATTCCTTCCTCTTCAG
Seq C2 exon
GGTATAATCCAATGATCCCGGCAGAAAATATAGAAAATGTGGTGAAGCATGTTGTCTTGGTTCACCAATCCGTGGACCACTACAGCCAACAGTTTCTACAGAAATTGAGGCGCAGCAACTATGTCACTCCCAAGAACTACCTTGATTTTATTAACACCTATTCAAAATTGCTGGATGAGAAAACTCAGTGTAATATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653:ENST00000409039:53
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:
PF127802=AAA_8=FE(10.1=100)
A:
NA
C2:
PF127802=AAA_8=PD(21.3=85.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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
  • Pre-implantation embryo development