Special

HsaINT0015081 @ hg38

Intron Retention

Gene
ENSG00000185344 | ATP6V0A2
Description
ATPase H+ transporting V0 subunit a2 [Source:HGNC Symbol;Acc:HGNC:18481]
Coordinates
chr12:123748575-123751229:+
Coord C1 exon
chr12:123748575-123748785
Coord A exon
chr12:123748786-123751109
Coord C2 exon
chr12:123751110-123751229
Length
2324 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
CTCACCTTCTGCACTAACAGGAG
3' ss Score
7.78
Exon sequences
Seq C1 exon
GCACTTCAGGAAGAAGTTCAACATTTACCTGGTTTCCATCCCGGAACTTCTCTTCATGCTCTGTATCTTTGGATACCTTATATTTATGATTTTCTACAAGTGGCTGGTTTTTTCAGCAGAAACCTCCAGAGTTGCTCCCAGCATTCTGATTGAATTTATTAACATGTTTTTATTCCCAGCCAGTAAAACAAGTGGCCTTTACACAGGGCAG
Seq A exon
GTGAGTCATCTTCCCACCCTCATGAACTTAACGGAAGTATTCCCAATAGTCTTTTATTCTGAGCAGTAGAAGTGTTGGGGTGATCTCCACAGGAGCCTGGGAAGGCTGCTTCTGTCTCTGCATGTGTCATCACTGGAGGATGCCAGTCCAGCTTGACCGCTGTGTGCAGGCAGCATGACCAAACTCGCTGCCACTCAGTAGCCATCAAAACGAGTAGGAAGAGGCCAGGCATAGTGGCTCATTTCTGTAATCCCAGCACTTTGAGAGACCAAGGCTGGCGGATTGCTTGAGCCCGTGAGTTCGAGACCAGCCTGGGCAACACAGCAAGACCTCATCTCTACAAAAAACACAAAAATTTGTCAGGCATGATGGCTGCACCTGTAGTCCGAGCTACTTGGGAAGCTGAGGCAGGAGGATCGCTTGAGCCCAGGAGGTCCAGGCTGCAGTGAGCCATAACTGCACCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAACCAAAACCAACAAAACTGGTGGGAAGAAAATGCATTACCAGAGGGATCCTGAGGGCTGCCCAGTCCCCCCATTTAGAAGGGACCACCTGGATCACAGCACATGGACCCTTTCAAAAAATGAGCTTTCCTCTCACTGTGCGTTTGTGTGCTGTCACAGTGGGCTCTAAGGGCTGACTGCTCTGCTTGGAGGCCCCGCTCTGCTGTTTCCTCAGGATGGAGCTTTGAGCAGATGACTAACTTCTCTCTGCCTCAGTTTCCTCATCTGTAAAATGGGACTAAAAACAGGAGCTGGTTCATAGTATAGCGCACGTGTCCAAAGTGCGTACGAACGTGCTTGCACAATCCAGCTACTCAGTAAATGTCAGCATTTGCCATAGTTCTTACCCACCTTACATTGAGGGTCTTTCTGCTGTGAGCGCCACGGCATCTCCTGCCCACGGATGCTGGTCCAGACATGGCTCACCACGTTGTAAAGTGTCTGTGAGGACATCTGGGGAAACCCTCCCAGTCGGTAGTATCAGAGCCTGTGTTCCTCCTGAGCCGTGTTTTGGTTTTTCATCGTGTTGACCTGTGAATGGAGCATTTGGTTTTGTTTTTCACATTCTATTGGGTGCTGGAAAGTTTTAAGTCAGATTTGAAGCTCAACTTAACGGAACTTTGGCCTCGTTGACGAGATGCATATTTGCGTTCTTTTTGAACTTTTTGTTTCTGTTTTTTTTTGGTTTCTCTTGTTTATGATTTTTAAGAATTGTATTTTATCATTATTTTATTGAAGCTTTGTACAATGGCATAGATACCACAGATAAATGCAGGGGCGTTCAGTGGGCACAGGTGCTATGGACAGAAAGATCAAGGAAGGGCAGCTACCTTTCTTTACTACCTGCCGCATACCTGAGAGTGTGCTTTCCTTACTTAGTGTTTCTTAATTCTCACAACAGCCCCAGGAGGTAGGTGTGTCATCCCCTGTTACTGGTGATAACTGGTGGCTCAGGGCAGTCCTGGTCACTCAGCGGTCTGTAGGGCCAGGCTGTTAACCTAGGTCAGCCTGGCTCCAGCCCAGGACTTCTGATGTGGCTCTGCCTGTGGCCGCCACCTTTCTCGGCATTTCAAGAGGTTCATCCTGTTGATGGTGTGTAGATAATACAGCTTTGTGCCTGAGTAGCACACAGAGCTCTAGGAACCTGTTTTTGGTGAGGGGCGACCATACAGAGTGATAAGCTTGGACAGCACAGTGTCCCGTCCAAACCCTGGGAAGCCATGCAGACTGCCGTGGCTGTGTAAGCCTGAGTGGATTTTGCTTTTGATTTAGCTTTAAGTAACTATAAATCTTCGTTTTTCTAAGGAAGTGTTTTTGGTTTTGTTCTGAATTCTCTTCCACGATTTTCTGTGTGTGGAGGTAAATCCACTTGCTGATTCACACTCATAGTCCTCAGACGGTCTTTATAATCATCAAAGAACAGGAAAACAGAACCAAGAATATACAAAATATTCTGCTTGTGCTTATACTTTCTCATTTACAGTGTTTACAGAAAATGATTAGTTGGAGTTTGACTCTCTTTAGAATTTTTGTAAAGTTTCCTTGCTGGTCTAAAACAAAATAATACTTTACCACAGGGTCATTAATGTTATTCATCAGTTCTAGAATTCAGCTATGAGTTTAGGAAAAGAAAACCCGCTGGCAAGTGTAGCTGGCTGGCATTTATTGAATGTTCCTCGCGTGGAGACATTGTTCGATCTTTCCTGATTTCATCGTGTGCTGCTGACCCTGCAGGCAGGCCTTCACGTTTTAATCGGGTTTCTCACCTTCTGCACTAACAG
Seq C2 exon
GAGTATGTCCAGAGAGTGCTGCTGGTTGTCACAGCATTGTCTGTCCCTGTCCTCTTCTTGGGAAAGCCACTGTTTTTGTTGTGGCTTCACAATGGGCGTAGTTGCTTCGGGGTGAACCGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185344:ENST00000330342:15
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(8.6=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(4.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development