Special

RnoINT0028938 @ rn6

Intron Retention

Gene
Description
calpain 1 [Source:RGD Symbol;Acc:2267]
Coordinates
chr1:221349728-221351358:-
Coord C1 exon
chr1:221351301-221351358
Coord A exon
chr1:221349793-221351300
Coord C2 exon
chr1:221349728-221349792
Length
1508 bp
Sequences
Splice sites
5' ss Seq
AACGTGAGG
5' ss Score
5.31
3' ss Seq
TTGTTTGTTGTTTGTTTCAGACA
3' ss Score
10.39
Exon sequences
Seq C1 exon
GACATGGAGATCAGTGTCAAGGAGTTACAGACCATCTTGAACAGAATCATTAGCAAAC
Seq A exon
GTGAGGATCCTCCCACCCCCGCACCCGTCTTGTTCCCAAATCACTCCGATTGCCTTGTTCTTGCTCCCACATGGAACTGAACCCCACACCTTGTTGAGGTGGCTGGCAAGGCTTCCATTGCCTGACCCAGTTCCCCAGACTCCTCACTAACCCCGCTCCACTCCAGTCTACTCACCTGAGCTCTGTGGCCTTAGGGAGAACAGACAGCCCATAGCAGAGCCAGCTCCAGGTGCTCAACACCAGTGAAAAGACAAGGACCTCCAGGCCAGGCTCCGTGCCTTGGGAAGCAGAATAAGATGAAATCCCAGGCCCTCTCCTGACCTGCCTTTCCCTCCTGGCTTCGGCTGCCGCATGTGGACATCCGCCTGCTCTCTTGCCTGTGGTTTGTTATGCCTGACCTCTTGGTGCACACCTCTCAGCCCAGGACCTCTCCTTGGCCCTCTCCAGCCTGCAGCCAGCACCTGCTGGTTCCTCTCCCACCTAAGCTCTCGTGTGTCTGCTCAGTACTTCCTTCCTTTCATTCTGGGCCAGTTGGTGGATACAGACGTGCTTCTGGGACTCAGATATGCTCTGCTATTTCTCACAATAACAGCATTCCCCCAACACGTTGCTGGCCTCAGCATCCATGGCAGGACTCCCTGGCACCAGTCAGTCCAGGGCTCCCAGCATGATGGGTTCTAAAGACTCCTGGAACTTGTTCCTTCTACATCTCGGTCGTCTCTCTCTTGGCAGATGAGGACGACATCAGATGCCCTGCTCTGTCACCTTCTGCTCTATACCCTGAGTCAGGCTCTCTCAGCCAGCAAGGCCCAGCAATCCTCCTGCCTCTGCCCCCAACATCACTGCAGTTACAGATCGTTTGAGTGTATAAGTGTGTGTGTGTATGTGTATGTGTGTATAAGTGTGTGAGTGTGTGTGGTATGTGTGTATGAGAGTGTGTGTGCACTCGTGCATGTGGGAGGGTATGAGTGTGAGAGACTGTGTGTATAAGTGTGAGTGTGTGTGAGTATATGTGCGTGTTTGTGTATGTGAGAGACTACCCACACCTTTTCATGTGGATGCTGTGGATTTTTAAATTTTTATTATATTTGTATTTTATATGTATAAATTTTTTGCATGCATGTATGGATACCAAATGCATGGATCACATCCCTTGAACCTGGAGTTGGGAGCCACTATCATTTGCATGCTGGGAATTAAACCCAGGTCCTCTGCAAGAGCAGCCAGTGCTCTTAACTGCTGAGCCATCTCTCCAGCCCTCCCCTTCTTTCTTTCTTCCTTTCTTTTCGTTTTTAGACAGGGTCTGTATAGCTGAGGCTGGCCTCAAACTCCTCATCCTCCTTCCTTCTCCTCCCAACTGCCATGGTTACGTTACAGGCATGCATTTCCATGCTTCGTTAATGCAGTGATGGGGATCAAACCCGGGGCTTCATGTATGCCACACAAGCATTCAATCAATCGAGTGATATCCTCAGCCCCCAGAACCGTTTGTTTGTTGTTTGTTTCAG
Seq C2 exon
ACAAAGACCTGCGCACTAACGGCTTCAGCCTGGAGTCGTGCCGCAGCATGGTGAACCTCATGGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000020935:ENSRNOT00000028431:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF138331=EF-hand_8=FE(31.1=100)
A:
NA
C2:
PF138331=EF-hand_8=FE(34.4=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
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]