Special

HsaINT0020750 @ hg19

Intron Retention

Gene
ENSG00000156030 | C14orf43
Description
chromosome 14 open reading frame 43 [Source:HGNC Symbol;Acc:19853]
Coordinates
chr14:74193307-74193675:-
Coord C1 exon
chr14:74193533-74193675
Coord A exon
chr14:74193411-74193532
Coord C2 exon
chr14:74193307-74193410
Length
122 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
TCATGCTCCTGTGGATCCAGTGG
3' ss Score
3.73
Exon sequences
Seq C1 exon
ACGGATCAACGTGGGCTCCCGGTTCCAGGCAGAAATCCCCTTGATGAGGGACCGTGCCCTGGCAGCTGCAGATCCCCACAAGGCTGACTTGGTGTGGCAGCCATGGGAGGACCTAGAGAGCAGCCGGGAGAAGCAGAGGCAAG
Seq A exon
GTGAGGAGGGGCCTGGGGGCAGCAAGTGAGGGCAGGCACATGGGTGGGCCAGGCCTCACCCTGCCCAGCCCCGCCCTGAACGTGGTTTCCTCCCCTCCCTCCTCATGCTCCTGTGGATCCAG
Seq C2 exon
TGGAAGACCTGCTGACAGCCGCCTGCTCCAGCATTTTCCCTGGTGCTGGCACCAACCAGGAGCTGGCCCTGCACTGTCTGCACGAATCCAGAGGAGACATCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000156030-C14orf43:NM_001043318:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.061 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0144819=ELM2=PU(79.3=93.9)
A:
NA
C2:
PF0144819=ELM2=PD(19.0=31.4)


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:
ACGGATCAACGTGGGCTCC
R:
TGTCTCCTCTGGATTCGTGCA
Band lengths:
242-364
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