Special

HsaINT0049240 @ hg19

Intron Retention

Gene
ENSG00000197653 | DNAH10
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:2941]
Coordinates
chr12:124333277-124335623:+
Coord C1 exon
chr12:124333277-124333429
Coord A exon
chr12:124333430-124335434
Coord C2 exon
chr12:124335435-124335623
Length
2005 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGA
5' ss Score
9.22
3' ss Seq
TCTTCCTTCTTGCCCTCCAGTTT
3' ss Score
10
Exon sequences
Seq C1 exon
GCCGTGGGGAAGATTTTCTCTGGCCTGGCACAGTGCGGGGCTTGGGGCTGCTTTGATGAGTTTAATCGAATCGATGCTTCTGTGCTCTCCGTGATCTCCTCCCAGATCCAGACGATCCGAAATGCTCTGATCCATCAGTTAACCACGTTCCAG
Seq A exon
GTGAGACACATGAAGCCCCCGGGACCATGTCCCTAGGATGGAAGTTTGCCAAGTATGGTAAGCTTCCTCTGTAGCGTCAGTTTCTGGGCCGTTGACACTCCAGACCAGGCTTCCTGTAGAAGATCTGTTGGTTTTTCCAATTGAGATGATTGGGTTTCCAAAATTATCATCATTGATGATAAGGTTTGTAATAGTCCAAGGACTTCACACTGACTCCAGACACAGAACCAATAGTTATGAATGGGCGTGGGGCAGAGTTCTCAAATAAGTGATGTGCAGGGTCCCCTAGAAAGGAAACAATATTCTTGGCGACTTCCCAAGTTTGAGAAAACCTGACTTAGAAAGCGAATGTTCCTTGCAATCATTATCACAGTGAACAAGAAATTTTGCCTTCATACCTTGTGAAGTTACGGCATCATAACAAGCAGGATTTGCAAGGTTATCAAAGTGAGAAGGCAGAATTTTAAAACAATTGTTGAGAATTCACCAATTTCTCTCTGCCAAAGAATATGTTTGCAGACTTGAGTTTGAGAAGTCTGCATTAAATTACACCAGATTAAGCTGGATCCAAATTTGGAGAAACATGATCTTATTATGTAATCTAGGTGGCCCAGAAGGGGATTCTCTGAAAACACAGGACCAGCGTGGGTGGGCCATTTCCCTACACCGGGGTCTTCTGGGTCCCTTGCTGTCCTTCTGCCTCTGTCCTCCCCCCTCCATGCCCTGCACACTTGTCACTAAGCCACTTGCTCCACAGTCATACCATGCCTTGTGACACCACATGTGTCCCCATCTGAGTGGAATTGTCCCTTCTTCCCTTCACTGGAAAACTCCTATACATCCTTTAGAGCCCCATTCCAGGATGAAAATTCAGCTTGAGCTGGTGGCCCTGTCATCTCACATGCGTCCTCCTCAGATCTTGGCAGGGCTCACTGTTAAGAGATTGTGTCAGCTGGAGACTGTTCAATATTTTCAGGATTCCAGTAAAGGGTCTGGATAGATTTCCCTTTGATGAGTTCTTTTGAGGGATTTTTGGGGCTGAGCTGACTGCTCCCGAGAGAGGGAATTAACCTGCAATGTATATAGATTTCCAGAAGCTGTGTTTCTCAGAGCCAGGAGGCAGCAGCTATCTGCTCTTCCCCCTGGGCCATCTGGGCCATCTGGGCCTCTTGTGGGATACTGAGGCTAGGGATGGTCTCAGGGCCGACCTATGAGTCAAGGCAGTGGCCTTGTTTTGGGGGAGGCTGGCTGTCTTCCGGGCTGCCCTCTCGTTGGTGATGCAGACTGTGCCTCCTAACAACAAAAATTTTCTGTCCTCTGCCTGGCTGGTGGACAATCAAAAAAAATAAAATAGAAAACTTCACCGAGAGACGACCGGACTCAACCTTCAGCTAAAAAGGCTAAGAATATAGGGATTTCCGTGGTTTGTTGGTACCTGGGGCAACCAGAGGAATGAAGACTGGTTTCTTGAGGGGTTTGAGGTGGGATTCTTTAGGCAGGAGTGACTGCATGAAGTCCAGGCACCCGCAGAAGGTGCAAAGCCAGGTGAGAGGAATGGAAGCCGGCGCTGTGTGAGGTGGTGGGCTGGGCGCTCCCAACCTGGGCTGTCTCCTTTCATCGCCACAGCCGTGCCACGAGGTGGGTTGCATTTCTGTTGTGCAGAAAAATAAACTGAGACTCAGAGAGGTTAAGTGACCTGCTGAGGGTCACACAGCTTCTTGTATCAGCCCCAGACTCTGTGCTTCGCCAACCTGGGCCCCTTCTCCAAGGTAGTGCCCTGGGTTCAGGTCTGAGTTTGGGGTTCCACTGAGACCTGCCCTCCCCAAGGCCTTCAGCGAGGGGGGCCCTGCATTGAACACCGGGGAGGGAAAAAGAGACAAGTGGTGTTGTCAGCCTCATACCATGAAAATGAATCGCCACGCAGCTCGCCGCAGGCCCCCTTTCCAAGGGGCTGGCCGGCCGGGCCACCTAACTGCTTCTTTCTTTCTTCCTTCTTGCCCTCCAG
Seq C2 exon
TTTGAAGGGCAGGAGATTTCCCTGGACTCCCGCATGGGCATCTTCATCACCATGAACCCCGGCTACGCAGGCCGCACGGAGCTGCCCGAGTCGGTGAAGGCGCTGTTCAGGCCTGTGGTCGTGATCGTGCCCGACCTGCAGCAGATCTGTGAGATCATGCTCTTCTCTGAGGGCTTCCTGGAGGCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653-DNAH10:NM_207437:33
Average complexity
IR-S
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:
PF127742=AAA_6=FE(21.6=100)
A:
NA
C2:
PF127742=AAA_6=FE(26.8=100)


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