Special

HsaINT0000741 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr17:69301139-69302906:-
Coord C1 exon
chr17:69302718-69302906
Coord A exon
chr17:69301287-69302717
Coord C2 exon
chr17:69301139-69301286
Length
1431 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGT
5' ss Score
10.28
3' ss Seq
TTAGTGTTTGTATTTTTCAGGTC
3' ss Score
10.74
Exon sequences
Seq C1 exon
GTATTTTTTGCTTTAATGCTGACACCTCTTTTTAAAAAATCAAAACATGTGGGAATAGTTGAATTTTTTGTTACTGTGGCTTTTGGATTTATTGGCCTTATGATAATCCTCATAGAAAGTTTTCCCAAATCGTTAGTGTGGCTTTTCAGTCCTTTCTGTCACTGTACTTTTGTGATTGGTATTGCACAG
Seq A exon
GTAGGTAATATATTAATCTTGCATTCACTAAATATTTTCTTTCTGTTTTATGTAGCTTCTTATACTACCATGAATACTACCTTTGATTTACCAAAAAAATTATTTTAAAATTTTAGCATGAGGAAGAAATGATTTCTAGAGTATATTTTATATCTAGTTTTATTTATGTTTGTCCAATTTTAAGTTTTTAGTTAAATGTTCTGTTTATAAATTTTTTACTTTTTACTTCAGTGTATCTCAGTGATTTATTTCACTGCAGAAACTCAGTTTGATAGTAATGTGTTTAAATGTCAAGTAATTCTTATTGCCTATGGCCTGGTTATATTGCTATCATTTGTACATTTATCTCAGAAGAATGCATGGGAGAAAATTGTGTGTGGAGCAGAACAAATTTACCGTGAGTGTAGTGGTGGAATAAGTAGGCCTGGTGGATTTTGTTGGCCCAGGCTTCATGGAATTGTCATTCAAAATAACATTCAGACTTACAAATATTATTTTTATTAGTCCTTACAGGAGTAGTTAGGTTCTAAATGGAAGAAGTCTTATAAGAAATGGCTTTGTAGTGGAACATGAATTTGGCTAATGTACAAAGAAAAAAATGTAATTACTAAATATAAGAAATTACTCATGTTGGTTGGATAGAAGTTCTGATTTATGAGATATAATTAAATATTGAGTTAATCATTTTACTTTTTTGAGACCTGAGAATGATTGTTATACATTTTGAGAGTTCATTGAGTCCCCGAGTCCGCGTTCTCTAGGAACGAAGAATTATAGATTCATAGGTTTTTGTTGTGAGTGGGATGGCCTTTCAGTGTCATTGAATTTATCTTCTTCATTTTATAAATGAGAGGACTGAAGCCTAGAATAGTATAATTAAAGCGTATTCACTTAATGGCAGGGCTAGGACCTAAATGAGGCTTCAACCTCCAGTACATTTCTCTTTCCATGCTATCACAAATATCTACTATGAATACTTTAATAATTGTGTTAATTAATCAAAATACTTGCTTTTCTCTATTGGAAAGATGCTAACCTAATTTTATTCCCTAATACTTAATTTGTTTGGCTTTCATATGGATCATAACCCTTTTGTTTGCATTTGTTATTATTAATATTGCAGTTTGTTTTTATTTCATTTGTTAGTAATTACATTGGAATTAAATGCCCCTAGAGTGAATATATCCCAGTTAAAGAAGCACAACATTAAAAACATGATTGAAAGGAATTGGTTTGATAAACTTACATTTTTGTAAAGTCTTTATTGTTTTCCTTATAAATTTATATTATTAATTTGGTCAAGTGTTTAATCTATTAAAAGGCCCAGTTGGTTACTATCACTCTGGATATGCTAAATAACTCTTAAGTAGTGTTAGCTTTTGCTTGTTTTTGTCATTTTTATGTAATAAAGTTAGTGTTTGTATTTTTCAG
Seq C2 exon
GTCATGCATTTAGAAGATTTTAATGAAGGTGCTTCATTTTCAAATTTGACTGCAGGCCCATATCCTCTAATTATTACAATTATCATGCTCACACTTAATAGTATATTCTATGTCCTCTTGGCTGTCTATCTTGATCAAGTCATTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154265:ENST00000392676:8
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:
PF126982=ABC2_membrane_3=PU(48.2=93.2)
A:
NA
C2:
PF126982=ABC2_membrane_3=PD(10.9=84.0)


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:
TTTTGCTTTAATGCTGACACCTCT
R:
TGACTTGATCAAGATAGACAGCCA
Band lengths:
326-1757
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