Special

HsaINT0000763 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 6 [Source:HGNC Symbol;Acc:36]
Coordinates
chr17:67084308-67085683:-
Coord C1 exon
chr17:67085606-67085683
Coord A exon
chr17:67084400-67085605
Coord C2 exon
chr17:67084308-67084399
Length
1206 bp
Sequences
Splice sites
5' ss Seq
ATAGTAAGA
5' ss Score
4.74
3' ss Seq
CTGTATTTCTTTGCTCATAGCCC
3' ss Score
7.58
Exon sequences
Seq C1 exon
AGAGACCAGGAGCACTACAGAGAATTTCCAGAGGCAAATTTTGAATTGAGTGCCACTGATTTTCTAGTCTGCTTCATA
Seq A exon
GTAAGAAGGGCTTTCCACCTCAGCACACATTCTTTTGGATGACTGTCATTCACTATAACAATTTGATCTTGTCCAAAGTGTGCCATTTTGAAAGTGTTTTTATATGATCTTAGATAAAGCACTTACCTTCAGACATGTTTCTAAACCTTAGAGTTACTTTTTACATGCTTGGATTGGCTATATGTGTCCAAAAGTTAATATTAAATTAATTTTTTGTTTGCTTATCCTGTTTACTGTCCCTCCTCTAAATTTGAGAGAGCTTGTAAAAAATAGAGATGCAATATAACTTACTTCCTTTGAATAATAGATTAAAAAGGCAAGAACTGAATAATAAAAGTGAAAGGGAAAATGATTATTTTGGTGTATTTAGGCTGAAGGGAACTACTGTCTTTGAATCCTATGTGTCAGTACTTTTCTAGGTACAGGAGAAAATAAAGACAGCGGTCCCTGCCCTCATGGAGCTTATATTCTGGTGGAAGGACATGGATAATAAACTAAATGGATAATATGTGTGGTGTCAGATGGGTGGTCAGGAAAGGCTTCGAGAAGAGCACTTCAGTAGGAAGTGGCAAGAGTGACCCCGGCTCAATCCAGGGTCAGCCAGGCCAGTGTGGTTGTGACTGAATGACCAAGGAAGAGAGTGATAAGAAAGATGGCCACAGAAGTCATGGGATAAAGCGAGAGGTCAGGAGAAAGGGTCACACAGGGTAATCTAGATTACTCTAAAGGCTTTGACTCTACTCTGAGTGATGGAGGAGGAGTCATTGGAGGGTTTTAAGCACAGTGATAAGTTCAGGCTTATGTATTAAAAAAGTAGCTCAGGATACTGTATTGAGAACAGATGTTTAGAACAAGAGGGGCAGAGATAGCCCAAGTAGGAAGGGGTTGCAACAATCCAGGTGAGACATTATAATGACCTAGGCCTGGGTGGGAGTATCATGAGTAGGGGTGAGAAATAATTGGGTTATGGATAATTTTGAAGATAGAGTAGATAGAATTTACTTACAAACTGAATATGGGTGGCGAGAAGAAAGGAAACAGGTTTCACTAACCTGGATTGTGAATGTATAGCTACATTTCTCCCCCAGCTTATGAGAATGATCCACAACTATTTACCCAAAGACAAAACACCACCAACTTAATTCAAATATTTAAATAATATTTGTGAACTTATGCCTAAATATAACTGTATTTCTTTGCTCATAG
Seq C2 exon
CCCTACTTTCAGACTTTGCTATTCGTTTTTGTTCTAAGATGCATGGAACTAAAATGTGGAAAGAAAAGAATGCGAAAAGATCCTGTTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154262-ABCA6:NM_080284:27
Average complexity
IR-S
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=FE(6.9=100)
A:
NA
C2:
PF126982=ABC2_membrane_3=PD(2.8=32.3)


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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development