Special

MmuEX6099904 @ mm9

Exon Skipping

Gene
Description
retinoid X receptor alpha [Source:MGI Symbol;Acc:MGI:98214]
Coordinates
chr2:27566103-27596723:+
Coord C1 exon
chr2:27566103-27566220
Coord A exon
chr2:27592819-27593084
Coord C2 exon
chr2:27596573-27596723
Length
266 bp
Sequences
Splice sites
3' ss Seq
TGCCAATTCTTGTCTTGCAGACT
3' ss Score
9.21
5' ss Seq
CAGGTAAGT
5' ss Score
10.86
Exon sequences
Seq C1 exon
CAGGAAGAGGAATCCACATGAGGATAGTGAAGCTGGAGATGAGTACTATACACTGTCCAAGGTAGCCGGTGAAGAAGAAGCAGGTCTACAGGAGGAGGCTGAAGTGTGAACCCAAGAG
Seq A exon
ACTTCTCTACCCAGGTGAACTCTTCGTCCCTCAACTCTCCAACGGGTCGAGGCTCCATGGCTGTCCCCTCGCTGCACCCCTCCTTGGGTCCGGGAATCGGCTCTCCACTGGGCTCGCCTGGGCAGCTGCACTCTCCTATCAGCACCCTGAGCTCCCCCATCAATGGCATGGGTCCGCCCTTCTCTGTCATCAGCTCCCCCATGGGCCCGCACTCCATGTCGGTACCCACCACACCCACATTGGGCTTCGGGACTGGTAGCCCCCAG
Seq C2 exon
CTCAATTCACCCATGAACCCTGTGAGCAGCACTGAGGATATCAAGCCGCCACTAGGCCTCAATGGCGTCCTCAAGGTTCCTGCCCATCCCTCAGGAAATATGGCCTCCTTCACCAAGCACATCTGTGCTATCTGTGGGGACCGCTCCTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000015846-'4-7,'4-5,6-7=AN
Average complexity
A_C2
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=NA A=0.899 C2=0.482
Domain overlap (PFAM):

C1:
NA
A:
PF118253=Nuc_recep-AF1=PU(69.8=91.0)
C2:
PF118253=Nuc_recep-AF1=PD(28.4=64.7),PF0010513=zf-C4=PU(15.7=21.6)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Human
(hg38)
No conservation detected
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
Chicken
(galGal3)
Zebrafish
(danRer10)
HIGH PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGGAAGAGGAATCCACATGAGGA
R:
CTGAGGAGCGGTCCCCAC
Band lengths:
268-534
Functional annotations
There are 1 annotated functions for this event
PMID: 11162439
Encodes an experimentally validated Eukaryotic Linear Motif (ELM). Method: mutation analysis, protein kinase assay. ELM ID: ELMI001406; ELM sequence: GRGSMAA; Overlap: FULL


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]