HsaINT0000763 @ hg38
Intron Retention
Gene
ENSG00000154262 | ABCA6
Description
ATP binding cassette subfamily A member 6 [Source:HGNC Symbol;Acc:HGNC:36]
Coordinates
chr17:69088167-69089542:-
Coord C1 exon
chr17:69089465-69089542
Coord A exon
chr17:69088259-69089464
Coord C2 exon
chr17:69088167-69088258
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:ENST00000284425:27
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=FE(6.9=100)
A:
NA
C2:
PF126982=ABC2_membrane_3=PD(2.8=32.3)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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