Special

HsaINT0000708 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr17:69291216-69294713:-
Coord C1 exon
chr17:69294655-69294713
Coord A exon
chr17:69291327-69294654
Coord C2 exon
chr17:69291216-69291326
Length
3328 bp
Sequences
Splice sites
5' ss Seq
GAAGTAAGT
5' ss Score
9.82
3' ss Seq
CTTCTTTTTTCCTGAACTAGATT
3' ss Score
7.41
Exon sequences
Seq C1 exon
AATTAGTGGTATTCAGAAGACATACAGAAAGAAGGGTGAAAATGTGGAGGCTTTGAGAA
Seq A exon
GTAAGTAGTTTTCCTAGTATTCAGGCCATAGTATTTAAAGTACAACTAGAAAAATAATTTGCATAGCTTGTGGGAAATTTAAACTTCTCTACCATGATTTTCTGTCTTGCTTTTATTTTATTTTATTTTTTTTGAGATGGAGTCTCGCTCTGTCACCCAGGTTATAGTGCAGTGGCGTTCTCTTGGCTCACTGCAACCTGCGCCTTCTGGGTTCAAGTGATTCGCCTGCCTTAGCCTCCTGAGTAGGTGGGATTACAGGTGTACGCCACCATGCCCAGCTAATTTTTGTATTTTTGTGGAGACGGGGTTTCACCAAGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGGTTCGCCCGCCTCAGCCTCCTAAAGTGCTGGAATTACAGGCATGAGCCACTGCGCCCAGCCCCTGTCTTGCTTTTTTGAGATACTTTCGTTTATGTGATTAATATTCAAAATAAAACTAACAACATGACATTTGTAAAAGTAAAATGTAGTATCTATTAAAATGAAAAATACTCAATTATTTGAATAAGGCTATGTCCTTGTTTCAGTTTATTATTTTGCATGTATATGCAATACATGTTAGTTACTTTTTGAAAAATTCATTTGGCCTATCGTAGGGTTTTTCAACCTCAGCACTACTGACATTTTGGTCCTGATAATTCTTTGTTGTGAAGAACTGTTCTTTAATGTAGAATGTTTAGCATTGTGTCAATGTGTTAGTCAGTCCCCAGAACCAATAGAATACACACACACACAAACACACACACACGCACACACACACACACACACACACACACACACACACACACCAGTATGATTGTAGGGTGGGGGATTAGGGGAGGTTTGTTTTAAGTAATTACTTCATGAGATAGTGGGCCCTGGTAAATGTAGAAATCTGTAAGGCAGGTTGGAAACTCAGGCAAGTGTTGAAGTTTCAGTCTTGAGCTCAAAATTTGTAGACAGGCTGACAGGCTGCACACTCATGTAGGAGTCTGTTACATTCTTGAGGCAGGACTCTTCCAAGGAACCTGTTTTTTCTCTTAAGGCCTTCAACTGATTGGATAAGGTTTACCATTATTATCAAGACTAATCAAGTTTAACTCAGATGATTATAAAAGTTAATGACATCTACAGCAACTTCTACATCAGTATTTGACCAAATAACGGCACCATAGCCTAGCCAGGGGGACCCATAAAATTAACCTTCACAAGCAGCATCCCTGGCTTTGATCACCAAAGAGAGAAGGAGTTCTGCCTCAAGAATGAAACAGATTCTTGCGTGAGTTTCCAGCCTGTCAGCCTATGAATTTTGGACCCAAGATGGCAACTTTAACTCTTGCCTGAGTTTTCAACCTGCCCTACAGATTTTTGGGACTTACTAGACCCCACAATCTTCTGAAGCAATTTCTTAAAATAAACCTTCCCTAATCCCCCAACCCCACACTCATACTTGCTCCATTGTGTGTGTGTGTGTGTGTATTCTGTTGGTTCTGGAGACTGACTGACACGCTGCTAAACATCCCTGGCACACTGCTAAACATCCTCTCCCAGTTGTAACAACCAAAAATGTCTCCAGTCTTTACCAAATGTCTTCTAGGAGGCAAATTAATTTATTAAGAAGAAAGTAGGTATAGTGGTATACTAATAGGGTTTTAGTTTGCATTTGCCTAATAACTAATGTTATTAATCACCTTTTTATATGATTATTGGCATTTGGAGGTTTTCCTTTATGAAATGCCTATTCAAGTTCTTTTCACATTTTTGTTTCAAGACCTTTGTTAGATACAGGTATTTAAATATTTGATCTCAGTCTGAGGCTTGCCTTTTAATTCTACTAGCAGTGTCTTTTGACAAACACAAGTCTTAATTTGAATGAAGTCCAATTTATGAATCTGTTCTTTTATGGTTACAGTGCTTTTCACGTCTTTTTATTCAACATTGGAGATTATATATAACCTCCAATGTAAGTTATTGGTACAACTAGTTAAGTATAATTATAATTGTAATAACAATTACAACTAATTGTTTCTAATGCAAAGAAGCAAGAGAATGAAATAAAAGGCATCCAGATTGGAAAGGATGCAGTAAAATTATTTGCAGTTGACACAATAATCTATTTTTAAAATCTTTTAGATTGACAAAAAATAATAGTGGAACTAAACAGTGAGTTTTGCAAGATGATAGGATACATGATAAATAATGGAAAAATCAATTGTATTTCTATATGTTACCAACACATAATTGGAAATTAAAATTAAAAATAGCATTTAGCATCAAAAAATATGCTTACAGGTAAATAAGACAAAAATGTAAAAGACATATCCTGATAAGTCCAAAACATTGCTGAGAGAAATTAAAGAAGATTTAAATAAATAGAAATACCACGTTCATGGGGCAGAACACTTAACGTTTAGTTGTTGAGTTCCCTTTCTTATTTTAACTTAGATTATTGGCGTTAGGATCTGAGACTTTTTCCTTCTTGTTTTATATGTTAGCCTTCTTAGTCTAGTTTTTGTTGTTGTTTGTTTGTTTTTGAGACAGGGTCTTGCTCTGTCCCCCAGGCTGGAGGACAGTGGCACAGTCTTGGCTTATCATAGCCCTGACTTCCCAAGCTCAGGTGATTCTCCCACCTCAGCCTTCCGAGTAGCTGGGACTACAGGTGCCACCATGCCCAGCTAATTTTTATATTTTTTGTAGAGACGGGATTTCGCCATGTTGCCCAGGCTAGTCTCGAACTCCTGGGCCCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCACGAGCCACTGTGCCTGGCCAGCCTAGTTTTTTGATAAGCCATTTCTGCTTCATCATTTCAGGTCCCCATCTCCTGTCTTCCTTCATTCCTTTACATATCCATTCAGTGATATTGCTTCATTAAATCTAACCTTTCAAGCCATTTCTATGCTATTGGTTAATTTCTTGTTTTTTTGCCAGTTTATTTAAATGCCTATAAATATCCTTGGGAACAAATTTTTGTTTAATTCCATTGGTTCCATTGGTAATTCCCAAAAATTGGGACACAGAAAATTCCCAAATATTTTGTATACTCTTAAATCTTACTGTATGAACAAATAAAGTTTATTTTTATTTACTTTCATTACTGTTTATATCGTTGACTGTAACAAAGAAGCTGTTTTACCTGCTATCAAATATGCTGGTAACTTTAAATATGTATTTATAGATATAGTGCCTTGAAGATTGCTCAAATATTATGAATTATCATGCATAGCTGAACAGACATAAAAATTACATTTGAGTCTTCTTTTTTCCTGAACTAG
Seq C2 exon
ATTTGTCATTTGACATATATGAGGGTCAGATTACTGCCTTACTTGGCCACAGTGGAACAGGAAAGAGTACATTGATGAATATTCTTTGTGGACTCTGCCCACCTTCTGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154265:ENST00000392676:11
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:
PF0000522=ABC_tran=PU(1.4=9.5)
A:
NA
C2:
PF0000522=ABC_tran=FE(25.2=100)


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:
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

  • Autistic and control brains
  • Pre-implantation embryo development