Special

GgaEX0010653 @ galGal3

Exon Skipping

Gene
ENSGALG00000007511 | F1NM67_CHICK
Description
NA
Coordinates
chr7:7143539-7144774:-
Coord C1 exon
chr7:7144569-7144774
Coord A exon
chr7:7144201-7144367
Coord C2 exon
chr7:7143539-7143961
Length
167 bp
Sequences
Splice sites
3' ss Seq
GATCTGGTTTTGATCCACAGAGT
3' ss Score
7.18
5' ss Seq
GAAGTAAGA
5' ss Score
6.42
Exon sequences
Seq C1 exon
TTCCTGCGTGGAGTGCAAGTCATTCAATAGTGGGCCACTGGCAAAGAACTGCTCTGTGGCCTGCACCAGCATCCAGCTGGCTGATGAGCCACGGGCAGGGAGTCGGCAGTGCAAGGAGAAGGACTCTGAGAACTGCTGGATCTCTTTCTATATGGCCCAGGATGATGGAGAGGAGATGTACACCGTCACTGTTGACCCTAAGAAAG
Seq A exon
AGTGCCCAGAGCCTCCCAACATCGCGCTGATCGTAGGCAGCACCATTGCCGGTGTGGCTCTCATTGGCCTGCTGCTCCTGCTGACCTGGCGGCTCTTGACAGAGATCTTTGACCGCCGAGAATACCGCAGGTTTGAGAAGGAGAAATCCAAGGCCAAGTGGAACGAA
Seq C2 exon
GCTGATAATCCTCTGTTCAAGAGTGCCACCACCACCGTCATGAATCCCAGATTTGATGGGCAATGAACTGGAGTGATGCCTGGAAGCACTAGGACCCACCACTAAATAAGGAAACACCAAACAAGGAAATCTCAGGCTCCCACCTCTTCTTCTTTATTGTGTTGTTTTTAACCCTTCTTCCAAGAGACCACCAGTAGCCAGGTGCTGGCTGAGGGGCTGCACAGTACCTATCCTCTCTCCCAGAGCCATCTGGTTGCACTGTAGGAGGAGGGAACAGCAGTGCCATGGACGGGGCTGCAGAGCAGATCTTACCAACAGGCACTCACCCCAGCTCCAGTTTCCATCTGTCCTAGCTCCTGGTGCTAACTTTACTTTGTGGCAGGACCTTCAGACACCAAGTCCCATAGGGACTTAGCACAGAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007511_MULTIEX1-9/10=8-10
Average complexity
S
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms (No Ref, Alt. Stop)

No structure available
Features
Disorder rate (Iupred):
  C1=0.043 A=0.000 C2=0.238
Domain overlap (PFAM):

C1:
PF079657=Integrin_B_tail=FE(86.2=100)
A:
PF079657=Integrin_B_tail=PD(7.5=10.7),PF087256=Integrin_b_cyt=PU(53.2=44.6)
C2:
PF087256=Integrin_b_cyt=PD(42.6=90.9)


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:
GCAGTGCAAGGAGAAGGACTC
R:
GAAGAGGTGGGAGCCTGAGAT
Band lengths:
250-417
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]