Special

HsaINT0000873 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 9 [Source:HGNC Symbol;Acc:HGNC:39]
Coordinates
chr17:69021742-69024353:-
Coord C1 exon
chr17:69024214-69024353
Coord A exon
chr17:69021862-69024213
Coord C2 exon
chr17:69021742-69021861
Length
2352 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACA
5' ss Score
8.88
3' ss Seq
GTTTTTGTATCCACTTTTAGAAC
3' ss Score
9.56
Exon sequences
Seq C1 exon
TTTGCATCTGAATGAAAGGTGTGATCCAGAGAGTATAACATCACTGGTTAAGCAGCACATCTCTGATGCCAAATTGACAGCACAAAGTGAAGAAAAACTTGTATATATTTTGCCTTTGGAAAGGACAAACAAATTTCCAG
Seq A exon
GTAACAAAATGTAAAGATGACAGAATGGTTTTGGAATGGTGTTATTAACAATAACAGTGGTGATAAGAATGATGGCTAGTTTTAATGCTTGCTAGATGAATGGCACAATGCGTTTACTCATTTAATATTCCCAACTCCAAGGTCACTTATAATATTACCCCTTAGTATTATCCATATGCTACTTATGAGTAAACCAAGGCATGTAGATGTTAAATATGCTTCAAGTCAATTAAGTGCAATTAAGAGGCGTAGGCTAGCAGCAAGATAAAATAAGAATTATTTGGAAAATTTGTTTCAGTAATGAATGAGAGAGTGTGGTCAGGGCAGGAACAGGTATATAAATACAGTGGCAGACTATCGAAGAAGAGCTGAAAGAATTGTACACAATAAATAGGTTGTTTTAGAAACACCAGCACATACTGATATAATCCAAGTTATTGAACATAACTTGGATTGGCGTGCATTCTGCCAAACACTTCAATGTACAACTTTGCTGCAAACACAGAAGCTTGGAGAACTACTGGTGTTATTACTTTTCTATGGTATCTCCCAATGCACTGTTTCACTTCCTAAGCGTTTTGAGGTAGAATGCTTCTTAAGTTTACTCTGTAAAAATGTGTTTGCCATATCAAGTTCAAGAAATTATACCGGGGCCATTGCTGCATGCTTGAATCAATAAGCATGACATAACCTTGGTCCATAAAGAAACACAGAACCAGACAATAAAGTGCAGAGATTGAAACTCAATGCTAGAGCCAGTCTAGATTCAAACACCAGCTATGCTATTATTAGCTCTATAATCCTTAACAGGTTATAGTACTATTCTGTATCTCAGTTTCCTCACTTGTGAAAAGAAAATTAAAATAGTACTCTAGGGTTGTTATGAGGATTAAATGATTTAATACCTTCAAATGTATTGAAATATTAAATATAAATAAAGCACTGGAACAATACCTGACATGCAGAACCTATGGTATTTCATCAGGTGTAAGAAGCCCTCAACTACAGGATGTACCACTAAGAAAGAAACACAAAGAAATAATGCTACCATTTAAAATATGATCTACTATCATTTAAGATCCATTATTATTTCAGATATATTAAAAGATGATGAAATATATCTCTTAGAATAAGTGAAATAATGGTTCACAGTGCATACACAATATCTTTGAGATATGTATCCTTATAAAAACAGAAATCTTTGTGAAGATCACACAGCAAAGTTTTAGCTGATTGCTTATTAAATGCATTCCAAAGTGGATGAGAAATTTGGAGAAAGACTGAAAAACAATTAACCCTTAGGTAAGTTTAAGGACTCATTAGAAATTTTGACTACATCTCTATTTTTCTTTGTCCAACACATAATTAAGATTGAAGTCTTTAATTTATCCCAATATTGAATTAGTTTATCTTTTATCCACCTTTCAGTTTTCCTGAATTTTCACACCATGGTCAGAAGTTGAAAGAGAGAGGGAGAGAGAGACAGAGAGAGGAGGTGCAAAGTTACATACATATTTTGTCCTTTTAAAAACTTTACATATTTATGGGCTGGGCGCGGTGGCCCATGCCTGTAATCCCAGCCCTTTGGGAGGCTGAGGCAGGCGGATCACTTGAGGTCAGGAGTTCAAGACAAGCTTGGCCAACATGGTGAAACTCCATCTCTACTAAACGCGCGCACACACACACACACACATACACACACACACACACACACACACAAAATTAGCCAGGCGTGGTGTTGTGCACCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGGATCACTTGAATCTGGGAGGTGCAGGTTGCAGTGAACCAAAATTGAGCCACTGCATTCCAGCCTGGACAACAAAGCAAGACTCTGTCTCAAAAAAAAAAAAATAGAAATTTTACATGTTTTTAAACTATCAAAGAGTCTATACTTAATTATTTCTATAAACATTAGTTCTTTTACATTTGTTATTATAATTCTCTAATAATTAATCTCAACAAGAAAGCACAAATCTCTATTCTCTGGAAAATATTTTTTTAATTAGTTGAAATTGAGAATTAAACACTCCCTGTAATATAACAAAAATAAATTTTAAAAAATATATTAAAATATGTTTTTCAAAAAACACATAGGTAGTTTCCTAAGAGTGAAAAAATAAATGTTTAGATTAGACTTTGATCTCAAAAAGACATGAAAAGTAACATACTATATGGATCATTTTAGAAATGAGATCATCTGTATCACAATTTTGTTTCTGATTAGTACATTTGGCCTATTACCAATATTTTACATTTTTGAGAAATATGGTTCTCATTATAAATTATATTCTTATAATCTGTTTTTGTATCCACTTTTAG
Seq C2 exon
AACTTTACAGGGATCTTGATAGATGTTCTAACCAAGGCATTGAGGATTATGGTGTTTCCATAACAACTTTGAATGAGGTGTTTCTGAAATTAGAAGGAAAATCAACTATTGATGAATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154258:ENST00000340001:17
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:
NO
A:
NA
C2:
NO


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