Special

HsaINT0015100 @ hg38

Intron Retention

Gene
ENSG00000105929 | ATP6V0A4
Description
ATPase H+ transporting V0 subunit a4 [Source:HGNC Symbol;Acc:HGNC:866]
Coordinates
chr7:138732877-138734254:-
Coord C1 exon
chr7:138734136-138734254
Coord A exon
chr7:138733094-138734135
Coord C2 exon
chr7:138732877-138733093
Length
1042 bp
Sequences
Splice sites
5' ss Seq
CATGTAAGT
5' ss Score
8.31
3' ss Seq
TGTGTGTCTTCCACCCCCAGATA
3' ss Score
11.56
Exon sequences
Seq C1 exon
ATTTGGAACTTGGCTTCAAACAAACTCACATTTCTGAACTCGTATAAAATGAAGATGTCGGTGATCCTGGGAATTGTCCAGATGGTTTTCGGTGTCATCCTCAGCCTTTTCAATCACAT
Seq A exon
GTAAGTTTCTTGATGCACTCTCTGCCTGCTCTGTCTGATCACACTGATGATGAATGGTGACAGAGCCACTGGTTTGGGAACTGCATCTCTCTGTGCAAGTTTTCTTCCTATGAGGGGTACTTCCCTGGGCATCTGGGCTTGAGCCAAGACAAGCTGGTTGGCTGGAAATGGCAGCACCTCCGTTTCTCCTGAGCAGAGTCTCTCCAAGGTAAGTGCTCCTCTGGCCCCAGAAATATTTGAGGGTTCAAAAAAAGACTGGAGGCCAGGTGCGGTGTCTCACACCTGTAATCCCAGCGCTTTGGAAGGCCGACAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAAGCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGTCGGGCACCTGTAATCCCAGCTACTTAGGAGGCTGGGGCAGGGGAATCCCTTGGACCTGGAGGCAGAGGTGGCAGTGAGCCAAGATTGTATCGCTGCACTCCAGCCTGGGTGACAGAGTAAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAAAAAGAGAAACCATTCTTAACTTCCAGGCTGTACAGAATCAGATGATAGTCTCCATTGGCCTGTGGGCCACACTTTGCAGACCCCTATCTTAGAGCATTCTTAGGAAAAAGCTTCCAGGTCCCCATTATATATCCTCTTGCCTTTAAATGTGCAACTCTGAGCTAGGTCTGCATGCGAAGCTGTAGTCAGATCACCACCCTCTCTGTGTGGGCATGACCTTTGCTTTAGACGTTACTTCTAGACCGTGGTTCTCTCTGACTCTTTTGTGCAAAAGCACTTTCCAGTATTTCCTTTCAATTTTCTTTTCTATGCATCCATACAGGATTGCTGTTTGCTGGGGGGGTGGGGGGTGCCGTTGTTTGCCAGTAGTGCAAAAAAAAAAAAGATAGAACATTTTGTGCTTTTGTGCTTTGAGAGAATAATTAAGTCCTAACGTTCCCTTGATGTTCTATCTTGTGTATGTGTGTGTCTTCCACCCCCAG
Seq C2 exon
ATACTTCAGAAGAACTCTCAACATCATTCTGCAATTTATCCCTGAGATGATTTTTATCCTGTGTCTGTTTGGATACCTGGTTTTCATGATCATTTTCAAATGGTGCTGCTTTGACGTCCATGTATCTCAGCACGCCCCCAGCATCCTCATCCACTTCATCAACATGTTTCTGTTTAACTACAGTGACTCTTCCAACGCACCCCTCTACAAACATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105929:ENST00000310018:16
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(4.8=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(11.7=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:
TTTGGAACTTGGCTTCAAACAAACT
R:
TGATGTTTGTAGAGGGGTGCG
Band lengths:
334-1376
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