Special

HsaINT0015088 @ hg38

Intron Retention

Gene
ENSG00000185344 | ATP6V0A2
Description
ATPase H+ transporting V0 subunit a2 [Source:HGNC Symbol;Acc:HGNC:18481]
Coordinates
chr12:123724654-123726285:+
Coord C1 exon
chr12:123724654-123724791
Coord A exon
chr12:123724792-123726196
Coord C2 exon
chr12:123726197-123726285
Length
1405 bp
Sequences
Splice sites
5' ss Seq
GAGGTACTG
5' ss Score
7.67
3' ss Seq
TTTCATATGTTTATTTCTAGTTT
3' ss Score
7.68
Exon sequences
Seq C1 exon
GAGCAGTTGCAGAAGCTCGAGGTTGAACTGAGAGAAGTCACTAAGAACAAGGAGAAACTGAGGAAAAACTTGCTGGAACTGATAGAGTACACTCACATGCTGAGAGTGACAAAGACCTTTGTGAAACGCAATGTTGAG
Seq A exon
GTACTGAACAGCTCGTGAGGAAATACAGCTGTTTTTATAAACAGCTTTTTATAAAAATCTCATTCCCATAGGCTGTGTATTTTGCTATTAGTTCATATAGATATGTTGCTTCTTTTAAGAGATTAAATTTATTTATTTATTTAATTTTATATTTTGTTTTTGAGACGGAATTTTGCTCTTGTTGCCCAGGCTAGAGTGCAGTGGCACAATCTCGGCTCACTGCACCCTCCGCCTTCCGGGTTCAAGAGATTGTCCTGCCTCAGCCTCTCGAATAGCTGGGATTACAGGCGCCCGCCACCACGCCTGTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTATCAAACTCCAGACCCAGTTGATCCACCTTCCTCGGCCTTCCAAAGTGCTGGGATTACAGGAGTGAGCTACCGCGCCCAGATTTAAGAGATTAAATTTAAACCTTGGTTTTATTTTTCAGTTGGATTATATGACTTTAAATAAAGTTTTAAGAGCCATTTCCTGTGTTGGTTGTTTTCAGCAATTACAATACTAAATATTTATAAGATGGTTTAGTTTGTGGTTGAAAAAAATTTTTATGAGCATGAGAAAAAAATTGAATGAAGGATGTTGAACTCTAAAATTTACTTTTTCCAAATTGCTAAGTAAAGGAAGTAAAAGAATAATCTATAATTTCTAAGACTAGGTCAGACACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAAGCTGGAGGATGGCTTGAGCCCAGGAGTTCAAGACCAGCCTGAACATAGTGAGAATTAATATGAGACCTTGTCTATACAAAAAATAAAAAATTAGCTGAGCGTGGTGGTGCATACTTGTAGTCCCAGCTACCAAGGAGGCTGAGGTGAGAGGATCATTTGAGCCCAGAAGTTTGAGGCTGCAGTGAGCTATGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGTGAGACCCTGTACCCTGTATCTAAAAAAAAAAAAAAAGAAAAAAAATTATAAGAATAAAGAATAGTCCATGTAGTAGCACCTTATGGAGCTAAGTATAGAAGAGACAAGTGCATCTGTTCCAAACTTAGTTTCACTTGATATGATAGTGACCTTTGATAAAGTTACTCTATCTTGGATGAAGGCAATGAACTAAATTATAACTGTCTTTTATGTAAATGTCTTCAATTGGCTTACAAATAAAGGATGGGGAAGTTATCTTTTCATTTATGAGGATTGAGTTATAAATCTAAGTTACCTCAGAAGTCTTTGCACCCAGATCTAAGTAGTTAGTTAGGATGCCCTATAAACTTGTTTGAAAATTTGACATGAGAAATAAAGTGTCACTTTTAATGAGACACACTTGGTTTCATATGTTTATTTCTAG
Seq C2 exon
TTTGAACCCACTTATGAAGAATTCCCTTCCTTAGAGAGTGATTCTTTGTTGGATTACAGCTGTATGCAGAGGCTGGGAGCAAAACTGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185344:ENST00000330342:4
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:
PF0149614=V_ATPase_I=FE(14.0=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(3.5=100)


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:
CAGTTGCAGAAGCTCGAGGTT
R:
CAGTTTTGCTCCCAGCCTCTG
Band lengths:
222-1627
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