Special

HsaINT0000402 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 1 [Source:HGNC Symbol;Acc:29]
Coordinates
chr9:107550201-107550848:-
Coord C1 exon
chr9:107550707-107550848
Coord A exon
chr9:107550336-107550706
Coord C2 exon
chr9:107550201-107550335
Length
371 bp
Sequences
Splice sites
5' ss Seq
AAGGTACTG
5' ss Score
8.56
3' ss Seq
GGTGCTTTTTATCACTGTAGGTT
3' ss Score
8.4
Exon sequences
Seq C1 exon
TATCTTATCAAACATCCATGAAGTACATCAGAACATGGGCTACTGCCCTCAGTTTGATGCCATCACAGAGCTGTTGACTGGGAGAGAACACGTGGAGTTCTTTGCCCTTTTGAGAGGAGTCCCAGAGAAAGAAGTTGGCAAG
Seq A exon
GTACTGTGGGCACCTGAAAGCCAGCCTGTCTCCTTTGGCATCCTGACAATATATACCTTATGGCTTTTCCACACGCATTGACTTCAGGCTGTTTTTCCTCATGAATGCAGCAGCACAAAATGCTGGTTCTTTGTATCTGCTTTCAGGGTGGAAACCTGTAACGGTGGTGGGGCAGGGCTGGGTGGGCAGAGAGGGAGTGCTGCTCCCACCACACGAGTCCCTTCTCCCTGCTTTGGCTCCTCACCAGTTGTCAGGTTATGATTATAGAATCTAGTCCTACTCAGTGAAAGAACTTTCATACATGTATGTGTAGGACAGCATGATAAAATTCCCAAGCCAGACCAAAGTCAAGGTGCTTTTTATCACTGTAG
Seq C2 exon
GTTGGTGAGTGGGCGATTCGGAAACTGGGCCTCGTGAAGTATGGAGAAAAATATGCTGGTAACTATAGTGGAGGCAACAAACGCAAGCTCTCTACAGCCATGGCTTTGATCGGCGGGCCTCCTGTGGTGTTTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165029-ABCA1:NM_005502:45
Average complexity
IR-C
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:
PF0000522=ABC_tran=FE(32.4=100)
A:
NA
C2:
PF0000522=ABC_tran=PD(17.2=54.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCAAACATCCATGAAGTACATCAGA
R:
CAGAAACACCACAGGAGGCC
Band lengths:
270-641
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