RnoEX0101757 @ rn6
Exon Skipping
Gene
ENSRNOG00000020087 | Zfp90
Description
zinc finger protein 90 [Source:RGD Symbol;Acc:1563077]
Coordinates
chr19:38601968-38608779:+
Coord C1 exon
chr19:38601968-38602063
Coord A exon
chr19:38603494-38603527
Coord C2 exon
chr19:38607134-38608779
Length
34 bp
Sequences
Splice sites
3' ss Seq
TTTGGTTCTTTTTTTCGGAGCTG
3' ss Score
-2.31
5' ss Seq
TAGGTAAGC
5' ss Score
8.89
Exon sequences
Seq C1 exon
GGTATCAAGTCTCCAAGCCAGAGGTGATCTTCAAACTGGAGCAAGGAGAAGAGCCATGGATATCAGAGAGAGAACTCCAAAGGCCTTTCTGTCCAG
Seq A exon
CTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAG
Seq C2 exon
ACTGGAAGACCAGGCCTGACATCAAATCGTGGAGTTCCCAGCAGGGCGTATCTGAAGTATCCCACAGTGCAAATGTTTGGTCGCACGCCACATTCGGAGATATCTGGGGTGTCAATACCCAGAGGCACCAGGAGAGTTGGAGAAGACATCTTGGGCCAGAGGCATCTTCCCAGAAGAAAATAACCGCTCTGGAGAAAATAGCTGAGCAAAATAAGTTTGGTGAGGACTCAGGTTTGAGCACAGACTTGGTTCCACAATTGGACGTTTCTTCAAGCATAAGGCCCAGCGAATGTAAGACATTTGGAAATAATTTGGAATACAATTCTGAATTAGTTACTCAGAGTGGTATCCCTGCTAAAAAGAAGCCTTACAAGTGTGATAAATGTAGGAAGTCATTTATTCATAGATCATCACTCAATAAACATGAGAAAATTCATAAAGACGATGCTTATTCCAATGGTACGGATCAAGGAGTTCCTTCTGGAAGGAAACATCATGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000020087_MULTIEX1-4/4=3-C2
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact
In the CDS, with uncertain impact
No structure available
Features
Disorder rate (Iupred):
C1=0.121 A=0.750 C2=0.232
Domain overlap (PFAM):
C1:
PF0135222=KRAB=PD(0.1=0.0)
A:
NO
C2:
PF0009621=zf-C2H2=WD(100=4.2),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.0),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7),PF134651=zf-H2C2_2=WD(100=4.7)
Main Inclusion Isoform:
ENSRNOT00000027209fB17021


Other Inclusion Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAGTCTCCAAGCCAGAGGTGA
R:
CGATTTGATGTCAGGCCTGGT
Band lengths:
119-153
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]