Special

HsaINT1015773 @ hg38

Intron Retention

Gene
ENSG00000170144 | HNRNPA3
Description
heterogeneous nuclear ribonucleoprotein A3 [Source:HGNC Symbol;Acc:HGNC:24941]
Coordinates
chr2:177217705-177219159:+
Coord C1 exon
chr2:177217705-177217845
Coord A exon
chr2:177217846-177219036
Coord C2 exon
chr2:177219037-177219159
Length
1191 bp
Sequences
Splice sites
5' ss Seq
GTGGTAAGC
5' ss Score
8.15
3' ss Seq
TAAAACCTTTCTGATTTCAGGTA
3' ss Score
8.96
Exon sequences
Seq C1 exon
GTGGCAACTATGGCGGTGGTCCTGGTTATAGTAGTAGAGGGGGCTATGGTGGTGGTGGACCAGGATATGGAAACCAAGGTGGTGGATATGGTGGAGGTGGAGGATATGATGGTTACAATGAAGGAGGAAATTTTGGCGGTG
Seq A exon
GTAAGCATTCACTTGTTTTATTTAAATGTTAAATATTCAGTGTTGCTAACAGTTCCCATGACACATATTTGGAAAGTGTTAAAAGCGTTTGATCAAATTTTATGTTCTATAAGAAAAATACTAAAATGGTTGGTAGTTCAAACCAAATTTTCTTGACTTTGCTGGTTATTTAGTAAAATGTACAAATGTACTCAGCTCTCTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCATTGCAATCTCCGCCTCCCGGGTTCATGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCGTATGCCAGCACGCCCGGTTAATTTTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCTGCCCGCTTCTGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACTGCACTCAGCCAAATGTACTGAATTTTTAGTTGAGTAGTAAAAAATGGACATTTACCAGTATTCAGTACATGTTTTACGTGTAAAAGATTGGGAGTTTATTTATTGCCAAAATTTTACTTAACTCCTTGGTACTTTTAAACTGGACAACCGGGAATAAATTGTTTGAATACTCCAGACGTGTTGAAGTGAGCAGGTTGCCATCTAGGGCCCAGGTTAACAAAGTACTTTGGGTCTTAATATAATATGTCACAGGTAGTTGAAGCGTTTAAGCAAGCTAGTGTATGTAGGTCATTAAGCCACAATACTGTTAAAAGCTTTCTTAGGAATGCACTGTTTTATTGGACCTAATTAACATGTCAATGACAGATGAGTGGAAGTTTTAACAAGTTAGAATGCCTTCTCATTGTTTTAAATGTTATACTGCTTCAGAATCATAGTGAATGGAACACTGGCAATTTTAATGGTGTTAATGGTAGAGAGAACATGCGCCTAGAGGACAGCATTTAATATAAACAAAATGTTGATGGTCTTTTAATATCCTGACATCAGTTACCCCAAGTGGTGCTACCACAGTGATGTGTATAAGCATGCTACCATAATTCTCAAAAGATAATAGTTACATACGTTAAAAGGGGAAAATGATGATTGTGTAGGTAAACCACACATAAAACCTTTCTGATTTCAG
Seq C2 exon
GTAACTATGGTGGTGGTGGGAACTATAATGATTTTGGAAATTATAGTGGACAACAGCAATCAAATTATGGACCCATGAAAGGGGGCAGTTTTGGTGGAAGAAGCTCGGGCAGTCCCTATGGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170144:ENST00000392524:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.438 A=NA C2=0.757
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF116273=HnRNPA1=PU(94.7=85.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGCAACTATGGCGGTGGTC
R:
GGACTGCCCGAGCTTCTTC
Band lengths:
254-1445
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains