Special

RnoEX0004789 @ rn6

Exon Skipping

Gene
Description
ATP-binding cassette, subfamily A (ABC1), member 16 [Source:RGD Symbol;Acc:1563534]
Coordinates
chr1:190205908-190222104:+
Coord C1 exon
chr1:190205908-190206035
Coord A exon
chr1:190212042-190212183
Coord C2 exon
chr1:190221845-190222104
Length
142 bp
Sequences
Splice sites
3' ss Seq
CTATTTGTTAATATTTTCAGGTA
3' ss Score
8.1
5' ss Seq
CTGGTAAGC
5' ss Score
8.69
Exon sequences
Seq C1 exon
TTCGAGGGTTTCCTTCAGAAGTTGAGTTTGAGGAGTACATTCTGTTCGATTATACGTCTCAGAAAGTACTGGCTGCCATTGTTTTTGACTGTGATTTCAAAAACAAAACTGATCCTCTGCCACTTCAG
Seq A exon
GTAAAATATCACTTGCGTTTTGTTGGTGCACAGAGGACCATATGGTGGCCAGACAAGATAGGCTGGAAAACGAGACTTCTCTTTCCAAATCATCCTTCTCTAAAACCCAGGAATCCAAATTATCTTGACGGAGGAAGTCCTG
Seq C2 exon
GGTACATCAAGGAGGGATTCCTGGCAGTGCAGCATGCCGTGGACAAGAGCATCATGCTGTATCATGAAAGCCGTGCTGGGAAAGAGCTCTTTGAAAACATTGACACTCTGGTACAGAGGTTTCCATACCCAAGTCATCCCCAGGACAAACTACTTTGGATCTCCAGTCCCTTCATCCCACTAATGTTCATACTCATGTTCTCTTCCATCGTTCTTTCCATCATGCGATCCATTGTGTTTGAAAAGGAGAAAAGGTTAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000015783-'3-7,'3-6,5-7
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.021 C2=0.000
Domain overlap (PFAM):

C1:
PF126982=ABC2_membrane_3=FE(9.7=100)
A:
PF126982=ABC2_membrane_3=FE(10.9=100)
C2:
PF126982=ABC2_membrane_3=FE(19.9=100)


Main Inclusion Isoform:


Main Skipping Isoform:
ENSRNOT00000001933fB299


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg19)
No conservation detected
Mouse
(mm9)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTCAGAAAGTACTGGCTGCCA
R:
AGTGGGATGAAGGGACTGGAG
Band lengths:
252-394
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]