Special

HsaINT0015057 @ hg38

Intron Retention

Gene
ENSG00000033627 | ATP6V0A1
Description
ATPase H+ transporting V0 subunit a1 [Source:HGNC Symbol;Acc:HGNC:865]
Coordinates
chr17:42494334-42495188:+
Coord C1 exon
chr17:42494334-42494473
Coord A exon
chr17:42494474-42495033
Coord C2 exon
chr17:42495034-42495188
Length
560 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATG
5' ss Score
8.73
3' ss Seq
TTCTTTCTTCTGGTTCCCAGATG
3' ss Score
9.35
Exon sequences
Seq C1 exon
CTCCGTATACTATTATCACGTTCCCTTTTCTATTTGCTGTGATGTTTGGAGACTTCGGTCATGGCATTTTAATGACCCTTTTTGCTGTGTGGATGGTACTGAGGGAGAGCCGGATCCTTTCCCAGAAGAATGAGAATGAG
Seq A exon
GTAATGTTTAAGTTACATCTGCATTGAACTGAAATTTTATAATTTCCCAAGCATTCATTATGAAAATTATGATCTGGAAGTCTTTTATCCATGAATTTATCAAAAGGAAGTAGAGAAGTTATGTTCATTTTAACACCAAAGACGACATGTGCAAGCTGGAAGTGGTAGTGTGTGCCTGTAGTCCCAGCTACTTGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAATTCGAGACCAGCATAGGCAACATAGTGAGACCCCATCTCTAAAAAAATAAAAATTATTTAGGTTTGGTGCAAAAGTTATTGCGGTTTTGGCTGCCAAAAGAAATGGCCAAAACCGCAGTAACTTTTGTGCCAACCTAATAAAAAAATAGAGGCCACATCCTGTGAAAGTGACTGTCTCATTAGCATTGTATTTTGGTTTTTACTTCAAGCTCTCTGAATCAGGATGGGGTAAAGTAGTGCTGGAGAAAGGGGCAGGTATATTCTGAATAACATTGTCACAATGTGAGCTGCAGTGAGTACATTCTCATTACTTCTTTCTTCTGGTTCCCAG
Seq C2 exon
ATGTTTAGCACTGTGTTCAGTGGTCGATACATTATTTTATTGATGGGTGTGTTCTCCATGTACACTGGCCTCATCTACAATGATTGCTTTTCCAAGTCTCTTAATATCTTTGGGTCATCCTGGAGTGTACGGCCGATGTTTACTTATAATTGGAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033627:ENST00000393829:12
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(5.7=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(10.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTCCGTATACTATTATCACGTTCCCT
R:
TCCAATTATAAGTAAACATCGGCCGT
Band lengths:
294-854
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