Special

HsaINT0000723 @ hg19

Intron Retention

Gene
Description
ATP-binding cassette, sub-family A (ABC1), member 5 [Source:HGNC Symbol;Acc:35]
Coordinates
chr17:67257266-67257889:-
Coord C1 exon
chr17:67257776-67257889
Coord A exon
chr17:67257401-67257775
Coord C2 exon
chr17:67257266-67257400
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-ABCA5:NM_018672:24
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:
PF126982=ABC2_membrane_3=FE(19.4=100),PF128222=DUF3816=FE(21.4=100)
A:
NA
C2:
PF126982=ABC2_membrane_3=FE(23.0=100),PF128222=DUF3816=FE(25.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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