Special

HsaINT0000781 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:36]
Coordinates
chr17:69123239-69125035:-
Coord C1 exon
chr17:69124888-69125035
Coord A exon
chr17:69123408-69124887
Coord C2 exon
chr17:69123239-69123407
Length
1480 bp
Sequences
Splice sites
5' ss Seq
CCTGTAAGT
5' ss Score
7.52
3' ss Seq
GTTGCCTCTTGGTTAATTAGATG
3' ss Score
4.44
Exon sequences
Seq C1 exon
ATTATCAAACTGGATTATAACTTGAATGGTGTAATTTTTCCTGACCCTTCAGGAGACTCATATACAATGATAGCAACTTTTTCTATGTTGCTTTTGGATGGTCTCATCTACTTGCTATTGGCATTATACTTTGACAAAATTTTACCCT
Seq A exon
GTAAGTAATAGTGAGTTTTTCTCTGTCCTCTACAGTTATTAATTACATTGAATATATTTTTTAAGATTATATAGACTTTTAAAATGAATATTAAATATTTCCCATTTCAAACTAATAAGTTCATTATTTCTACTTCATAGTTCTAATGGTCTAATGAAATTTTTATGTAAAAACAATTCTTCTTATGACTTTACTATAGCAATATATTATAATTATATGACAACAATAATTATAATACATCTTGTAATTGTGTGGTAATTAAATAATGTTAGGTTTTCATGGATCCCTGAAAGTGTTTTGAAAGGGTCATATTAGGATTTATGTCAAAACAAGATAAAAGAAATTAGTTCTTATGGTGGTTTGGCTCTCGGGAGGCCATTATACTGTGGAAGAGCTTTCTCATGAATATTTGTTCAGCATCATTCTCAAAATGTTTTATATATTGTTCATATTTACAGAAGTATATTGATCGCCCAGTTAAATTATCTTGCAAACAACCAAAAATGTCACGTAAGCCCAGAATTTTTTCACACATTCTAGAATCAGAAAGCTTTTTTTCTGGCACAATCTTCTTGTTTATCCTCTTATTTTATATGTTCCTTCCACTATTTAAGGTTGTCTTATAGGTTTTCTATGTATTTACTTGTATATATTCCTGTCTTTCTGTGACTTCTGGTTGATATGTGAAGGCCCTTAATAATAAATTCAACTTTGTTTTTTAAACTGGAAAAATATATTTAAAATATCACTATAAATTTATTCTAAACAAATACAGTTTCTCCATGTATTCATGCCTAAGCAGGAATATATAGATTTCAATATTATGTTCAATTATGTTGCTGTGGTCAAATTATTTAAGTTGACAAACATGTCTACAATTATTTTTATGCACTGTATTAAGGCTTTGTGTCTTCCCAAATATTTGGTTTCATTCATTCTCCTAAATACCTTTTAGATCACATTTTAAAAAAATTTAATAAATATGTTTATTGGGTGATACAAATCTGTTTTTCATGAGCCTATTAAGGATAATGCAACCCATTGTTAAGACTGGAAAAAAAGGACATATAATGGTTTCCTTGTTGGGTGTCCTTTTCTACAGATGTAGACAACAGAGGCTCTAAGATCTGTACTAATGTCTTGATCAGGGAAAAGCTGGAGTCCAACTCAGCTGGTCATACACCTAATATTTTATTCGAACCTCACTTTCCTATTGACTTTCTTTTTTTTGATCACATTCTATTTATACTTTGTTGAAAGCTGTATTATATTGTTTAATTTTGCAATATGTTATTTCCTTTGAATTCCCATTGTTTACTTCATCATCAAGTTTTCTTCTTAATAATAAATTGAGTTTTAGAAGAAAAAATGTCTCTATGATGCTTAAAACTTCAAGGCATTCTGCATTGTTGTTAGCAAGGCTTCTTTGCGCATTCTTTTACTATTACTGATCATATTTTGTTGCCTCTTGGTTAATTAG
Seq C2 exon
ATGGAGATGAGCGCCATTATTCTCCTTTATTTTTCTTGAATTCATCATCTTGTTTCCAACACCAAAGGACTAATGCTAAGGTTATTGAGAAAGAAATCGATGCTGAGCATCCCTCTGATGATTATTTTGAACCAGTAGCTCCTGAATTCCAAGGAAAAGAAGCCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154262:ENST00000284425:9
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=0.035
Domain overlap (PFAM):

C1:
PF126982=ABC2_membrane_3=PD(10.8=84.0)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAACTGGATTATAACTTGAATGGTGT
R:
CTGATGGCTTCTTTTCCTTGGA
Band lengths:
311-1791
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