Special

HsaINT0000709 @ hg38

Intron Retention

Gene
Description
ATP binding cassette subfamily A member 5 [Source:HGNC Symbol;Acc:HGNC:35]
Coordinates
chr17:69289862-69291326:-
Coord C1 exon
chr17:69291216-69291326
Coord A exon
chr17:69290038-69291215
Coord C2 exon
chr17:69289862-69290037
Length
1178 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGT
5' ss Score
10.13
3' ss Seq
AATATATATTTTGCTTTTAGGGT
3' ss Score
8.72
Exon sequences
Seq C1 exon
ATTTGTCATTTGACATATATGAGGGTCAGATTACTGCCTTACTTGGCCACAGTGGAACAGGAAAGAGTACATTGATGAATATTCTTTGTGGACTCTGCCCACCTTCTGATG
Seq A exon
GTGAGTTTTCTGTCTTAAAGAAAAAAAAACTTCATTATATATATTCTTTAAATGTGTATTGAATAATTTTTGTCAATGGGACCAACTTCTGTATCTGTAAAGGTGTTTTCTTTTTTTCTTGATTATACACATGTGGTTGTTTTTAGTAGAAGATAAAAATGATTCTATCATGTTTAATAAAGTAAAAAGGATCTAATTTTGTACATATTTCTATACATATACACACGTAGATGTGTATGTATGTGTTTTTATTCATCATTTTCAAGGGAGGATAAATGAGTAACTTATTGGAAATTAAATCAGAACTATAGACTATTTGAGGTTGAGAAAATAAACACAAATATCTAAATATACAGCAATAGTTCAGCAGGAAATAATTGTAAATGTTCATACTATCTTCTAAAATAGAATTTTAAAGGCATACCTCAAAAGTATAATTTTGATATGTGATTGTTTGGTAGGTGAGAATTCATTATAGTAGCTCCATATTATGACAGTAACCAAATAGAGTGGCAGTACAATAAATATTTTACTTTACAAAAGGGCTGAATTGTATTGAATCTGCATTTCAACTCTTTAAATGTTATTTAACTTTTAAAATTAGTTTGATTTTGTTCTTTGTCCTTAGTTGTATCACTCTTTGATGGTAGTCATAATATCTTACATTTGTATAAGAATTTATGATTTTTCCTCATGATTCTTCATAATGTATGATTGTTTTAATTTTCACTATTAAAACAATGAATATATTAGTGTTCACTGTATAAAAAAGGAAAGCTGGAATTTAAAGAGATTAAGTAATTTGGCCATGACCACACAGCTAGTTAGGATAAAATTTATAGTTCTTTAATCCCTCCACTATTGCACAGTGTCTAGAAAATTGTTACTGGAATACAAGTGTAAATAGTGTATCAATAGATATTTATGTTTAGTGTCAAGCTTTTACTTTCTTGCTTTTCCCACTATGTTATATGACCTGTAAGTGATGGAAAATGAGATTGAAATATAAGTGGATGCGGATCACCAATAATATTGAAGGGTGTGTTGTGCCTTGTAAATTTATATTAATTTTTACCTTATATGTCTGTTATAACCAAATAACTAAGTTATCAGGATACTTGAAAACATACACATTATAAAATAATTAATGTACATTTAAATATATATTTTGCTTTTAG
Seq C2 exon
GGTTTGCATCTATATATGGACACAGAGTCTCAGAAATAGATGAAATGTTTGAAGCAAGAAAAATGATTGGCATTTGTCCACAGTTAGATATACACTTTGATGTTTTGACAGTAGAAGAAAATTTATCAATTTTGGCTTCAATCAAAGGGATACCAGCCAACAATATAATACAAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000154265:ENST00000392676:12
Average complexity
IR
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(25.2=100)
A:
NA
C2:
PF0000522=ABC_tran=FE(39.5=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:
GTCATTTGACATATATGAGGGTCAGA
R:
TGTATTATATTGTTGGCTGGTATCCC
Band lengths:
279-1457
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