Special

RnoINT0012605 @ rn6

Intron Retention

Gene
Description
actinin, alpha 1 [Source:RGD Symbol;Acc:70907]
Coordinates
chr6:103391950-103393554:-
Coord C1 exon
chr6:103393462-103393554
Coord A exon
chr6:103392181-103393461
Coord C2 exon
chr6:103391950-103392180
Length
1281 bp
Sequences
Splice sites
5' ss Seq
GATGTGGGT
5' ss Score
2.02
3' ss Seq
CCTCTGTCTCGACACCTCAGCTG
3' ss Score
4.24
Exon sequences
Seq C1 exon
GCGGAAACAGCAGCCAATCGAATCTGTAAAGTGTTGGCCGTCAATCAAGAGAATGAACAGCTTATGGAAGACTATGAGAAGCTGGCCAGTGAT
Seq A exon
GTGGGTACCCCCATGTTTGTTCTTCTAGCCTGGCCCCAGCAAGGCCCTGTATTATACCCTGAGAGAGTGAAGCCCCCAGGATCTGTACCTGTATTGTCATTCTGCCCACACAGTCCCAGGCTGGTGTAGTGCATGATCCAATCAACCACCATTAGCATAGGGCCGCTTGGTTCTGGGCCTCTGGGAGCGCAGAAGTGAAGTCGGGGAGATGGTCTCCAGGCTATAGTGGGCCTGGGAAATGCCTTCACCTCTCTGCCTCTTGCTTTCCTTCACTTACTGAATGGGAGTTGAGCCCTTTAGACCTCAGAGGCATTTGCAGCCTGATAAACTGCCCCTTGGGAAGGCTTGCCTGAACTAGATAGTACAGGGCTGTGCCAGGTACTTAGAAGACATGTGCCAGGGAGGGCTGAGTACTGTCTCAGGCTTGGTACTTAGCAGTACTTAGTACTTAGTAGTCAGGCCAGCAGGGGACAGGATGGGAAGAGGTTAATCAGCTGACCTGCTGTCCTTTGGTTAAGGTGCTGCTTGCTTCCTCCTTACAGACCTCAGCCCTTTGAACTTTTCCCCTGGCCGTTCAGTGGCTTTGCCCTCCAGCCGAGTGAGGAGAGCCAGTTGCCCCGGCTTTAATCCCTGCTTCACTGCTCCGGCCAGTCACTGCAGCAAGCTGCGTGACCTGGCAGAGCCTTGGAGACCTCCTCTACAGTGAGGGGGTGATCGTAGCACTTGACCATGTAGTATTTCTATGATTATTCCTGTGAGTCACTTTGTGGGTCATGCCTGGCAACGTGCAGGTGTCCCACCTGCTTCCTGTCATCCACCCTAGTAATCCTGCGTCTTCTTCCTCACCCTCACCATGGCTCCAGGATAGAAATCTAGGCTGTCCCAGAACCTAACCTCTTCCTCTGGGGCCAGAGGTTCCCGTTCTGTTCCACTCCTGCTTGGTGAAGATGAGGAAACCGAGGCCTGGCCAGACTTAAGCTCAGGTCTCCCTGCTTTTAAAGCAGCCCGTGGTTCTTTGGTTCTTCCTGTATCGGGGCAGAGAAGATGAGGGATGTGGGCTCTGAGCTGACCATATCCTGGTCAACTTGGAGGAAGTACCCAGAAGCCTTCCTACATGGCATGGTGAGGTCTTCGTAGGTAGTTGGTTGAAGGGAGTGTGCCATCAGGAGAGACTTTTTGCCAGCCCTCTTCCTGGGAGGGGAAGGCCTATGGAAAAAAGGCAAACTGGCCCTTGCACATCCTTACCCTGGTGCCCTTCTTTCCTCTGTCTCGACACCTCAG
Seq C2 exon
CTGTTAGAGTGGATCCGCCGCACCATCCCATGGCTGGAGAATCGGGTGCCCGAGAACACCATGCAGGCCATGCAGCAGAAGCTGGAGGACTTCCGAGACTACCGACGCCTGCACAAGCCGCCCAAGGTGCAGGAGAAGTGCCAGCTGGAGATCAACTTCAACACACTGCAGACCAAGCTGCGGCTAAGCAACCGGCCTGCCTTCATGCCCTCCGAGGGCAGGATGGTCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000056756:ENSRNOT00000079824:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0043516=Spectrin=PU(9.9=35.5)
A:
NA
C2:
PF0043516=Spectrin=FE(68.5=100)


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:
CGGAAACAGCAGCCAATCGAA
R:
GACCATCCTGCCCTCGGAG
Band lengths:
320-1601
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]