Special

GgaINT1011578 @ galGal4

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 7 [Source:HGNC Symbol;Acc:HGNC:18661]
Coordinates
chr7:9267328-9269977:-
Coord C1 exon
chr7:9269858-9269977
Coord A exon
chr7:9267512-9269857
Coord C2 exon
chr7:9267328-9267511
Length
2346 bp
Sequences
Splice sites
5' ss Seq
GAAGTATGA
5' ss Score
3.33
3' ss Seq
AAATATTGTATGCTCTTTAGGTG
3' ss Score
6.64
Exon sequences
Seq C1 exon
AAATTTACGCCTTCTTGACACAGATCTGTTTCACAATAAACAGGAAGCTGAGGAACTTGCATCTTTCCAGATTAAAGTCATCCAGGAAATTGGAAAATCCAAAGCTGTTCTATCTAGGAA
Seq A exon
GTATGATCTAGTGTATCCATATATTTTAAGTTACAGGGAAATCTTTTTCTTGGGGTGTTTTTGAGATTCTGGATTTTGCAGAGACAGAAGAAATGACCAGTTTTAATAGTACGCATTGAAGAAAGAAATGCGGTGTTTTGAAACGCTTTGAGGATAGTGAATGAAAGTATTTTTGTAAATGTTGAGCTTACTATGATTTGTCATTTTCTTGTTCTAAATTCTGCTGTGTTGTGTTTTGCTTTTTATCTCCTATAGGGCACAGATTCATTGAAAATTGGATAATTAGTGGGATGTGATCAGTATTTTAGTCTATTTTGAGAAAAAAGCTTTTATTTTGAGGACTCCCTTGTCATCTAATTGCTGTTCTTAAAAGAATAGTTGGAGCTATTTCAGATTACTCTGCTTTTTAAAGTTCCCCTGTTTTTTTTTCCTCCCTGTTTTCACACCATTGAAAACAGCTATAATACTGAATTTTGAAGAGATGCATTGAAAAAGTGCAGTGTTGCTACTATCAATAATTTTTGACATTAAAAGTAAATTGTGATGGAATTTATATGTAATAAGACTTGCTCCACCCCTACTTTAAAGAAAGCGCTGCCTATAGATAGGAGTAACTGTAATTACCCTAATGTTAGATTAATAACAACACCCATGTAGAACTTCTGTAAATGAGTTTGATATTTCAGTTTGTATATTCTCACTTTTTAACCATTTTTCAAACCAGCATCATCTAAAGAATATTTTTCAAAAACCCTCTTACACTATTGTATGGCAAACAGGTATACAGATTGTAAGGTATAGGACCAGACTGATTATCACATTGTAAAGGAAAAATGAAATAAAGAGCTTACCCATATCCTAGGCTCACAGAAGGATTCCAAGGGGGATGATCTCCAGATGGAGATCCTTCTTCCTTGGGAGTCAGCCCTTAAATGGGGTCTAGGAGGTCTGGTCACTCAGGTGAAATTGCATTCACCTGTGCCCCTGCAGCTGACTCAGCCCTTGCCTCAGGTGTTCAATCAGAGTTTCAGGCGGTGATTCAGCAGTTCCCATACACACTATAATGTCAAAGGATGTCATTAATAAAACAAAGTGTTTGAGCCCCATAATATTTGTATATCCATCCAGCAGAATTTCTGAAAGAAGGGCAGTTTTCTTGTTATTGTGCTCAATATGCTGCAGTAGAAGCACTGTAATTACTAGGTCTTTTTTAGATATTTGTAGCCATGCTGTATTGTTTGTATGCATCCGATCTTTATTCAGTAGTCACAGAATTGCAGGGGTTGGAAGGGACCTCTAGAGATCATCCAGTCCAACCCCCAGTGGTTGCTTCCTGCTATTATTTACTACTGCTCTTTTACTATTTTAGATTTTAATTAAGAAGAACAGCTGTTGTATTTACTCAATTCCTGATTGTTTAGGGTTGTGGTTTTTCTTGTTTGTCAGTTGGTTTTTTTTTTTTCATGTTATGGAAAGTTTTTATTTCCGCTTTTGTTTATAATTGTGTTAGTAACTACCTCAACTATTTTCATATGTATTTCTTTCTGACCCTGAAAATATCTTTGTGTTCTTAACTGAAGAATCATACAATGGCCTGGGTTGAAAAGGACCACAATAATCATAGAGTTTCAACCCCCTTGCTATGTGCAGGGTCACCAACCACCAGACCAGGCTGCCCAGAGCCACATCCAGCCTGGCCTTGAATGCCTCTAGGGGTAGGGCATCCACAACCTCTTTGGGCAACCTGTTCCAGTGCGCCACCACTCTGTGTGTGAAAAACTAATATCTGAGCTAAACTTCACCTGTCTCAGTTTAAAACCGCTCCCCCTTGTCCTATTACTATCCACCCTTGTAAACAGTTGTAATGCTGCATACTTTTGTGCTTTCATCTTTCCTATTTCGCTCCAGTGCTAGAGCCAGGTTGGCACAATTTTGGCTAAGAGTGGCAGGGTGGAGTTCTCTATGGAAAACTTTGGCATCTAAAATCTACTAAGGTTAAAAGATGGATAAGGAATTGTGTGGTCTCTGGGACTTAAGTATGCTGCCTATGAAGGCTTTCTGTTTTTGTGGACTTGAGAAATAGGAGACTAATGCAGTGGATTTGTCTGTCATGGTACTTTTTATTTTAAATATGGTTCCATAGTAGTAGATAACATTTTAAGATACATGATTCCTTTGAATTTAAAGGTACTACCATATGAGCTAGTTACGTTATAGCTTCCCAAGTATACTGTAGCATCTTTTGTTCATGCATGTACTTATAAGCATTCAGCAATTAACTTAAAACTGTAGGTTCATTAATACTAAAGACTTGAAGAACTTACAGAAATATTGTATGCTCTTTAG
Seq C2 exon
GTGGCTTCCAGAAGTGCAGAAAATCTTTTACCAAAGTAATAAAAAAAAGCAAATACCCAGTTATACCAGCACTGCTAAATTAGAGGCTTTCTTCAGATGTGCTGCCACTTTAATGACCCGTCAACTGCAACAATTACTTTTACAATCAATTCAGGACTTCACAGATTTAATTGTTCAACCAGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007841:ENSGALT00000012727:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]