Special

HsaINT0000694 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 4 [Source:HGNC Symbol;Acc:34]
Coordinates
chr1:94473791-94474427:-
Coord C1 exon
chr1:94474307-94474427
Coord A exon
chr1:94473854-94474306
Coord C2 exon
chr1:94473791-94473853
Length
453 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
GGTTTCTTCGTATCTTGCAGATT
3' ss Score
10.24
Exon sequences
Seq C1 exon
GATTGCCGAGCCCACTAAGGAGCCCATTGTTGATGAAGATGATGATGTGGCTGAAGAAAGACAAAGAATTATTACTGGTGGAAATAAAACTGACATCTTAAGGCTACATGAACTAACCAAG
Seq A exon
GTAAGGGAATGGGTATGAGTTTGGAGGTGCTGGTTAGATCCACAGTTGGCATGATGTTGCCATTTTCCTTCTATAGAACAATTGATATGCTTATGCAAGCAATTTGGTTCCCAGTTTTATGTAGGGTCATCATCCCTGTGTTATAACTCGTCTTCCAAGAGCATCTAATTCCAATGTGTGTTCCCTGCTATTCATCTCGGGCACTGACACAGGGCCTCAGTGAGAATCACTCCAGCTGAGCATCATTCCCTTTTCTGTGTTCTGTTTCTGCAGAGCATGGGTCAGCCTCGAGATGTCTCAGTACTCACCACACCTCTGTGCCTGCCCATGTCAATATGTAACCTCCTAGTGCTGGTAGTTTTCTCCTAAACCATCCTTTGCTCTTTGTTCCCTCTTCCCCTCCTTGCTCTCACCCTGTCTCAGTTCTCAGTCCGGTTTCTTCGTATCTTGCAG
Seq C2 exon
ATTTATCCAGGCACCTCCAGCCCAGCAGTGGACAGGCTGTGTGTCGGAGTTCGCCCTGGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198691-ABCA4:NM_000350:41
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.098 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0000522=ABC_tran=PU(7.6=52.4)


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:
GATTGCCGAGCCCACTAAGG
R:
CTCCAGGGCGAACTCCGA
Band lengths:
182-635
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