Special

GgaEX6024886 @ galGal4

Exon Skipping

Gene
Description
human immunodeficiency virus type I enhancer binding protein 3 [Source:HGNC Symbol;Acc:HGNC:13561]
Coordinates
chr23:862644-898680:+
Coord C1 exon
chr23:862644-866185
Coord A exon
chr23:869979-870124
Coord C2 exon
chr23:898505-898680
Length
146 bp
Sequences
Splice sites
3' ss Seq
TTGCTCTTTTGGGGAGATAGGTT
3' ss Score
-0.15
5' ss Seq
AGGGTAAGT
5' ss Score
10.45
Exon sequences
Seq C1 exon
CCCGGTCCGGTTCTCCAAGCTTTGAGGCGCTGGAGGAGTATCAGCAGCCAGCTGGCAAGCAGCCCCTTGGCAAGGCACCTTTACAAAGCGTGAAGAAAGAAGACTCCAAAGAGCCAGTGGAGCAGCCTCCACCAAGCCCTCCAAGCCCTGCACCTCTGTCCGAGGTCCCTTCAAGTGCAATGAAGTCTCGAGAAGGTACGGATATGAAGAAGGTACTTCAGTTCCCCAGTCTCCACACAACCACTAATGTCAGTTGGTGCTATTTAAACTACATAAAGCCAAATCACATCCAGCAAGTCGACCGGCGGTCTTCAGTGTATGCCAGCTGGTGTATTAGCTTGTATAACCCCAACCTTCCGGGTATATCCACTAAAGTCGCCCTGTCCCTCCTGAGGTCCAAGCAGAAGGTGAGCAGGGAAACCTACACCATGGCTACTGCTCCACGGCCAGAGGCAGGCAGGCTTGTCCCGTCCAGCTCCAGGAAGCCCAAAATGACAGAG
Seq A exon
GTTCATTTGCCTTCGCTCCTTTCTAATGAAGGTCGAAAAGAAATAACTAGAGCTGAGAAGGAAGAGGATAAAAGAGGAAAACCAGAAGAAGAGGCTGTTGTAACCAAAAGAGGGGAGCCAGTCAGGATCAAGATCTTTGAAGGAGG
Seq C2 exon
GTACAAATCAAACGAAGAGTATGTGTATGTGCGAGGCCGTGGAAGAGGGAAGTATGTATGTGAGGAGTGTGGAATTCGCTGCAAGAAACCCAGCATGCTGAAGAAACACATTCGCACGCACACAGACGTCAGGCCATATGTCTGCAAGTACTGTAACTTTGCTTTTAAAACCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000027365-'1-7,'1-1,3-7=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=0.684 A=0.571 C2=0.033
Domain overlap (PFAM):

C1:
PF139121=zf-C2H2_6=WD(100=2.3)
A:
NO
C2:
PF134651=zf-H2C2_2=WD(100=43.3)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGAGGTCCAAGCAGAAGGTGA
R:
GCAGACATATGGCCTGACGTC
Band lengths:
255-401
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]