Special

HsaINT0000732 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr17:69253573-69253869:-
Coord C1 exon
chr17:69253794-69253869
Coord A exon
chr17:69253668-69253793
Coord C2 exon
chr17:69253573-69253667
Length
126 bp
Sequences
Splice sites
5' ss Seq
AAGGTACTT
5' ss Score
8.4
3' ss Seq
ATCTTTTTCTTTCCATGTAGTTG
3' ss Score
8.53
Exon sequences
Seq C1 exon
AATAACACATGCACTTGATTTAAAAGAACATCTTCAGAAGACTGTAAAGAAACTACCTGCAGGAATCAAACGAAAG
Seq A exon
GTACTTTCATTAAACACCAAATAATGCCTGTATTTTTATTGATAGTTTAGTACCTGATATTGTCTTGATAGATTCCTTATAGTGAACCTTTGTTAATTTCCCACCCATCTTTTTCTTTCCATGTAG
Seq C2 exon
TTGTGTTTTGCTCTAAGTATGCTAGGGAATCCTCAGATTACTTTGCTAGATGAACCATCTACAGGTATGGATCCCAAAGCCAAACAGCACATGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154265:ENST00000392676:33
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=0.188
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=FE(17.1=100)
A:
NA
C2:
PF0000522=ABC_tran=PD(13.7=62.5)


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:
ACACATGCACTTGATTTAAAAGAACA
R:
TGTGCTGTTTGGCTTTGGGAT
Band lengths:
163-289
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