Special

HsaINT0003160 @ hg19

Intron Retention

Gene
Description
actinin, alpha 1 [Source:HGNC Symbol;Acc:163]
Coordinates
chr14:69350885-69351600:-
Coord C1 exon
chr14:69351492-69351600
Coord A exon
chr14:69351026-69351491
Coord C2 exon
chr14:69350885-69351025
Length
466 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGA
5' ss Score
7.66
3' ss Seq
ACCCTATTTGGCACTCCCAGCGG
3' ss Score
4.65
Exon sequences
Seq C1 exon
TGAGCTGGACTATTATGACTCACCCAGTGTCAACGCCCGTTGCCAAAAGATCTGTGACCAGTGGGACAATCTGGGGGCCCTAACTCAGAAGCGAAGGGAAGCTCTGGAG
Seq A exon
GTGAGAGGTCCCAGAGGGAGATCTAGGCCCATATCCGGCAGCCCTGTGGTGCCCCTTCCTGCTTCTTGACTCTCTTTGCTTTGGGCTAAAAGACTCTATGGCTTCCCCAGACCTCCCCCAACCCTGGCCTAAATGTGGAAGATTCACTTTGGCACAGGATTTGGACTTTGCCCTCATGGCGATGCCTCCTCTCTTGCCCTCACATGTCTCATCCTCCCAGTTTAGTGTGCTTTACAGCCCAACCCCAGCCATTTGAGAACCCTCCTATTCTACACACCAGACTCTGGGACCCAGGCCAGGTGACTGTGATGTGAGATGGTTCATACAGCTGGCAGGAAGAGCTTGTTCTTTCTGCCTGATTGAGTCAGTGCTTCTAGACCTGGGGCTCACCAGGAGGATCTTGATAGGAGTGGGGGATGATTCTGGACATCACTGTACTAACCCTTACCCTATTTGGCACTCCCAG
Seq C2 exon
CGGACCGAGAAACTGCTGGAGACCATTGACCAGCTGTACTTGGAGTATGCCAAGCGGGCTGCACCCTTCAACAACTGGATGGAGGGGGCCATGGAGGACCTGCAGGACACCTTCATTGTGCACACCATTGAGGAGATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000072110-ACTN1:NM_001130005:13
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.005 A=NA C2=0.012
Domain overlap (PFAM):

C1:
PF0043516=Spectrin=FE(34.0=100)
A:
NA
C2:
PF0043516=Spectrin=PD(0.1=0.0),PF0043516=Spectrin=PU(32.1=76.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGCTGGACTATTATGACTCACCCA
R:
GGATCTCCTCAATGGTGTGCA
Band lengths:
246-712
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