Special

HsaINT0000461 @ hg19

Intron Retention

Gene
ENSG00000144452 | ABCA12
Description
ATP-binding cassette, sub-family A (ABC1), member 12 [Source:HGNC Symbol;Acc:14637]
Coordinates
chr2:215851266-215852517:-
Coord C1 exon
chr2:215852371-215852517
Coord A exon
chr2:215851453-215852370
Coord C2 exon
chr2:215851266-215851452
Length
918 bp
Sequences
Splice sites
5' ss Seq
CCAGTAAGA
5' ss Score
5.9
3' ss Seq
TTCCCTTGATTTCTCTCCAGGTC
3' ss Score
10.64
Exon sequences
Seq C1 exon
GGACATACGGTATGGCAGCTCCCTGGTATTTTCCAATTCTTCCTTCCTATTGGAAGGAGCGATTTGGGTGTGCAGAGGTGAAGCCTGAGAAGAGCAATGGCCTCATGTTTACTAACATCATGATGCAGAACACCAACCCATCTGCCA
Seq A exon
GTAAGACAAGTCGGTCAACAGCGTGCTTTGTTATGAGAGAAATGATATGAAATTACATGACTAGTAGTTTCAATTATTTTTTTCTAAATGGCAAAATTATCATCCTTTTAGTCATGGATGAAAATGTCTACACATGCGTCTTTGGACTCTTATGGGGATTAAATTGTGGCTTTTTCTGGGCTCATTAGCTCAGTTGGTTAGCATATGGTGCTAATTAGGCCAAGATTGCAGATCCCTTTGTGGTCCAGTTAGACTCACACAGAGAAAAATTTTGTTCCTTGGCCACAATCTACACCCCTAACTCCAGCCATCTGTCACCAGTCATAAGGGGTAACCAAGTAACAAGTTTGAGTAATTTAGCATAACCCATCACAAATACTGGAAAAGTAGTTCAAAGCTTGTGTCTTCCTGATACTAGGTGAGTCGTGTCATTATAAAGTGAGTACGGGCCACTAAGCGGTCCTTTTGTGATGCCTGAAGGAGGTGTAGATAGTTATTAATGAACTGGATTCTATAAACCACAATCTCAACTAGTCTTATCACTCTAAAATCACAACTTTGGAGGCATTTATTTTATAATTTGGTATCATCCTGCCCAACCAGAGGACCAAGCCTTAGACATATCTTTTGACTATTTGATATCTGTTGAATAAAGGAGAATTTATAATTATAATACCATATTCTGGGACTGCTTTTTCCAACAAAGAAGGGTGAAATGAACCCTGGTTCTCCACTCTTATTCATTCTGCAACCAAGTGAGGAGGCTGAAGACTATAATAAATCATTTGTTTCTGGATTTTTTATTTTACTTAGAGGGTTATATTTTTATAGTCTTAAATTTTTAATAAAGATAAAGTCTAACTCTAGCTGCATTACCTTACTTGTGAGTTTACAACTCTTCCCTTGATTTCTCTCCAG
Seq C2 exon
GTCCTGAATACATGTTTTCCTCTAACATCGAGCCTGAACCTAAAGATCTCACAGTCGGGGTTGCCCTGCATGGGGTCACAAAGATCTATGGCTCAAAAGTTGCTGTTGATAACCTCAATCTGAACTTTTATGAAGGGCATATTACTTCATTGCTGGGGCCCAATGGAGCTGGGAAAACTACTACCAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000144452-ABCA12:NM_015657:19
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=0.048
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0000522=ABC_tran=PU(18.4=42.9)


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:
GGACATACGGTATGGCAGCTC
R:
ATGGTAGTAGTTTTCCCAGCTCC
Band lengths:
334-1252
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