HsaINT0000723 @ hg38
Intron Retention
Gene
ENSG00000154265 | ABCA5
Description
ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr17:69261125-69261748:-
Coord C1 exon
chr17:69261635-69261748
Coord A exon
chr17:69261260-69261634
Coord C2 exon
chr17:69261125-69261259
Length
375 bp
Sequences
Splice sites
5' ss Seq
GTGGTAAGT
5' ss Score
10.36
3' ss Seq
TTATTTATTTTTTTCTTTAGGCA
3' ss Score
10.54
Exon sequences
Seq C1 exon
GTTTTTTGCCTTATTGGTTATGTTCCATCAGTTATTCTGTTCACTTATATTGCTTCTTTCACCTTTAAGAAAATTTTAAATACCAAAGAATTTTGGTCATTTATCTATTCTGTG
Seq A exon
GTAAGTCACATTTTACATTATTTCAACTTTCCATAGCAGTTTAATTAACATGAATTCTTTCCTGATTATACTAAAAATGTTACATGTCTTTTGTAAGTGAATAATTTAGATAGGTAATTGGCAGCTTCTTTTTGTGTGTACATTTGTCTTCTGAATCATCCTTTCCACGTAGGAACAATATGGAAGAGATTTAGCAACTAGTGTATCAAGGATACTAGCTACAAACAAGTGGTATTCTTGTTGCTTGCTGGCTAAATATCATCTCTTGTTCCATGTTTTATTAGAGGATTGAAAAAATAGTTTAATGCGTAGACACCAATTTGTAAGAAGTTTCTAAACACTTTGTCACTTTTATTTATTTATTTTTTTCTTTAG
Seq C2 exon
GCAGCGTTGGCTTGTATTGCAATCACTGAAATAACTTTCTTTATGGGATACACAATTGCAACTATTCTTCATTATGCCTTTTGTATCATCATTCCAATCTATCCACTTCTAGGTTGCCTGATTTCTTTCATAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154265:ENST00000392676:25
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(19.4=100)
A:
NA
C2:
PF126982=ABC2_membrane_3=FE(11.7=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TTTTGCCTTATTGGTTATGTTCCA
R:
CTTTATGAAAGAAATCAGGCAACCT
Band lengths:
246-621
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