Special

HsaINT0003171 @ hg19

Intron Retention

Gene
Description
actinin, alpha 1 [Source:HGNC Symbol;Acc:163]
Coordinates
chr14:69376035-69376759:-
Coord C1 exon
chr14:69376672-69376759
Coord A exon
chr14:69376114-69376671
Coord C2 exon
chr14:69376035-69376113
Length
558 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
TCTTCTCTCTCCCCGGGCAGCTG
3' ss Score
11.1
Exon sequences
Seq C1 exon
AGACTTCAGCCAAGGAAGGGCTGCTCCTGTGGTGTCAGAGAAAGACAGCCCCTTACAAAAATGTCAACATCCAGAACTTCCACATAAG
Seq A exon
GTGAGTGCTGGGGTCTGAGGGGCTCTCACAGAACCAGGCTGCCTCCCCCGGGAGCTCCCAGACCCCCTTGGCTGGGTCAGTCTCAGCTTTAGAACAAAGTGGAGACCTCTGGGGGAAGAAGTAGCTTTCCTTGGGAAGGGGATGTCGCCATCGCTCTGAATCCCCCCGTCTCTCTCCCTGCAGTGTCTTAGATGGGGCTGCTGCCTGATATAACTTTGGTTGATGCTTTTGCTACTGGGAGCGCCCCCAAGGAAATTGTCCAGGAAGTCCCAGCCCAGGGCTCTGGAACAGCAGACTAGGGCCATAGGCCTTGGTCGGGGGTAGGGCTGGATATGGCAGGTTTATCTGAACTTGTCAACCCCCCCACAAAGTCTTGACCCTAGTGCCTGGGATTTGTGGCAGGAAGAAATGTCCCTTCCCATCCTGTCTTCTAACTCCTACCCCAGAAAGCTCTATGTGTTCATCTCTCTGGTGTCTAGGAGGCCCCTGCTTTGCCCTGGTTGCCCGTTTGTTCAGCCTCATTTACCAGCCTGCTCCTTCTTCTCTCTCCCCGGGCAG
Seq C2 exon
CTGGAAGGATGGCCTCGGCTTCTGTGCTTTGATCCACCGACACCGGCCCGAGCTGATTGACTACGGGAAGCTGCGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000072110-ACTN1:NM_001130005:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (disopred):
  C1=0.018 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0030726=CH=PU(24.0=83.3)
A:
NA
C2:
PF0030726=CH=FE(25.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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