Special

HsaINT0000436 @ hg19

Intron Retention

Gene
ENSG00000154263 | ABCA10
Description
ATP-binding cassette, sub-family A (ABC1), member 10 [Source:HGNC Symbol;Acc:30]
Coordinates
chr17:67149972-67150467:-
Coord C1 exon
chr17:67150376-67150467
Coord A exon
chr17:67150151-67150375
Coord C2 exon
chr17:67149972-67150150
Length
225 bp
Sequences
Splice sites
5' ss Seq
GTGGTATGT
5' ss Score
7.64
3' ss Seq
ACATTCATTGTCTTGTGCAGGTG
3' ss Score
10.71
Exon sequences
Seq C1 exon
GTGAAGTTTTGGGATTACTAGGACACAATGGAGCTGGTAAAAGTACTTCCATTAAAATGATAACTGGGTGCACAAAGCCAACTGCAGGAGTG
Seq A exon
GTATGTGACATGTGAAGGAAATTTTATTTTAAATATTGATGACATCTTTCTATTATTCCTATCAGTAAATCAAATATCTTTTTAAAAAATAGATGAAAGAATTTATAAAATTTCTCTTGCGTATTCAAAAAATATTGTAGCTTAATGGCCACTTTTATCTCCTTTAGTAGAAGGGGGATTGGAGCAAAAACCAAAGGTGAATCTGACATTCATTGTCTTGTGCAG
Seq C2 exon
GTGGTGTTACAAGGCAGCAGAGCATCAGTAAGGCAACAGCATGACAACAGCCTCAAGTTCTTGGGGTACTGCCCTCAGGAGAACTCACTGTGGCCCAAGCTTACAATGAAAGAGCACTTGGAGTTGTATGCAGCTGTGAAAGGACTGGGCAAAGAAGATGCTGCTCTCAGTATTTCACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154263-ABCA10:NM_080282:32
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.048 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0000522=ABC_tran=FE(20.4=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(40.1=100)


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:
TGAAGTTTTGGGATTACTAGGACACA
R:
CGTGAAATACTGAGAGCAGCA
Band lengths:
270-495
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