Special

HsaINT0000679 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 4 [Source:HGNC Symbol;Acc:34]
Coordinates
chr1:94495984-94496676:-
Coord C1 exon
chr1:94496552-94496676
Coord A exon
chr1:94496083-94496551
Coord C2 exon
chr1:94495984-94496082
Length
469 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCGC
5' ss Score
9.1
3' ss Seq
ACATGTCTCACTCTGTCTAGCAT
3' ss Score
6.29
Exon sequences
Seq C1 exon
ATCGTGCTCCCGGCTACCTTTGTGTTTTTGGCTCTGATGCTTTCTATTGTTATCCCTCCTTTTGGCGAATACCCCGCTTTGACCCTTCACCCCTGGATATATGGGCAGCAGTACACCTTCTTCAG
Seq A exon
GTGCGCGGACTCGGGGTCACCATTCTCCTCTGTGGGTTTGGGGCACCTGGGTCACATGCTGCTTAGAAGGGCCCTGACCTTCCCACTTCACTGGGACCTTCACCAATGAGAGAGGGGAGGGGTCTTTGGGCTGCCTGCAGAAAGGAACTTAATGTATCTGCCACTGCTTGGAAAGGCGATCCTAGTGGACAGGCAGGACTGCTTGGGAAGGCCGAATGGGGAAAGGAATGCAAAGCTTAGGTGAATGGGTTGAAGCGCCATCTTTTTGAGGCATAGGTGACATGCCATCAGACCACTGCGAGTGTTCAGGCAGCCTACCGCACTCCCAGGAGAGCTAGCGCCATCCCAAGGCAGCATTCGGTGCCTCCAATACATACCTGGCACACAGCAGCTATCCAGTAAAGGCTCTGAGTTGCATGATGTTGGCACGCGCCTGCTCTGTCCCAGTCACATGTCTCACTCTGTCTAG
Seq C2 exon
CATGGATGAACCAGGCAGTGAGCAGTTCACGGTACTTGCAGACGTCCTCCTGAATAAGCCAGGCTTTGGCAACCGCTGCCTGAAGGAAGGGTGGCTTCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198691-ABCA4:NM_000350:28
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
ATCGTGCTCCCGGCTACC
R:
GAAGCCACCCTTCCTTCAGG
Band lengths:
223-692
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