Special

GgaINT0007915 @ galGal4

Intron Retention

Gene
ENSGALG00000002056 | C15H22ORF25
Description
chromosome 15 open reading frame, human C22orf25 [Source:RefSeq peptide;Acc:NP_001007837]
Coordinates
chr15:1268713-1271124:+
Coord C1 exon
chr15:1268713-1268817
Coord A exon
chr15:1268818-1268926
Coord C2 exon
chr15:1268927-1271124
Length
109 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAA
5' ss Score
8.38
3' ss Seq
CTACCTTTATGTTGTTCCAGGAC
3' ss Score
9.66
Exon sequences
Seq C1 exon
TCAGTTACCTGACCCTGCAATTGAAGACCAAGGGAAGGAATACATACGTCCTATATTGAACAAGTATGCAGCTGTGTGTGTTCGTTGCCCGGGTTATGGAACAAG
Seq A exon
GTAAAATTTCCTGCTGGACCAAAATATATCTCAATTCAAATGCATGTTGCCACAAATGTTAACTCTTTACTGAGTGCTTTATATTTCTTCTACCTTTATGTTGTTCCAG
Seq C2 exon
GACAAACACAGTCCTCCTCATTGATTCAGAAGGAAACGTTACTTTCACAGAGCGCACCATGATCAATGAGGATGTCAGCCAGTGGAAAACAAGCAGCTATGAATTCAAACTGCACATGTAACAACTTTCCATTTGAATGCATTGTAATAAAAGCAATGAAAGCAAGCTGTTAAGCTCCAGGAAATGTTTTCTGTCAGCCTCTGGAAGCCAAAAATAGCAAGAGAAGCAAAAGTTGTTTTAAATAGGTTGTGTAAGCTATCAATCTCACAAATCCTCTGCATAAAACAAGTTTCTTACTGTTTTTACATTAAGTTGCAACTTCAAAACAAATTTCTGTCCATATGGCTTTGTTTTATCATCTAAGCTTAAAAAATTGTAAAACCCAGTGGAAAATACTAACAGGATACTGTACCTTGCATATAACTTCTTTATTTTTATTTCAGCCAGAGCTGAAAATATATGCAGCTTCTTGGAGAATCGACCTTCAGCTAACTTTCACAATCTAAATTTTGTCTAAAAATTAGATTTGTATCATGGAATTGAAAGAAAATCAGCTGCAGTTCCATTTCTTTTCACAGATTCCTCTAATTTCTTTTCGCTCAGATACAACCACGTACTGTATGATGCCTGAAGCCAATGTCTAGCAGTCATAGAACATAAGATCAGAGGGATCGTGAAGCCACCTGGCATATAACACCTGCTTCCAGGGCAAGGCTGCCTTTGTCCAACATGCAAGTCATTGCTTTGTTTTTTCTTTTAAGTATGTTTTAAAGAAATACCAAACTTGTATTCAATTCAGAGGAGGAGAAATGCTTACTGCTTTTGTTTTGTTTTTTTTTTTTACAAAACTGCTCTCCCTTCAATATGTAATTTTAAGATTGTAAGCTGATGCCAATATACATTAAATGAATGTATGTTTTCTTTGTAGCATTAAGTGTTTTAGTAATATTTAAACTTTTCCCTATGCCATGGTACACTGTTCTGCCTGGAGAGGGTGGGGAGGGAAGAATTTGTTTTGTTTACCTGTAAATAGTACAGCAATAGATCTTAAATACTCTCAAATCTAGTTTTAGAACTAAGAAATTAAGTTGTCACTGCTCAGTTCTATTCAGTAGAAGTTTAAAGTTGTTTATCTTTGAAAGGAATAAAATTCTGTACTGTGACATCTGGTTTCCTGATAATCTCATTAGCAATATTGTTTTTTTTTTTTCCTACCCCACCAGGCAGATAAGGAGTAATTATGCTTGCAAATGGACACTGAATGTGAGGTTACAGTAACTTGAGACAGCCTTAGTGATCTGCATACCTGGACATTGCAGTGGAGGTGAAATTTGTAGTAATCTATTTATAATTTCAAAGAAATCAATGGAGAATTCAGAACCACCTCTAGAATGGAATATCTGTTGTAATGTAACTTTTTTCAACCATGCTAAAAAGGTCATGCTACAGAATTCTTTATTTAATGTCTTGTTTAAGAGTGTATGTCTTTAAAAGTGGTCATACCACAAGGTTTGGGAGGGGAGCAAACAGACAAAAACCCTAGCAAATAGGGCTGTGAAGTTGATGTGTCTTCAGTGTCTTCACTGGAAGCAGTAGGTAGTGTCTTCAGTGGAAGCAGTAGGATTAACAGGCAAGTAAAAAGGAATAACCACCATGTTCTGAGTAGCTTTGATAAAATGCCACTTCGTTCAACATGCATTTTGTTTCCATCTCATTCTGTGATTGATATTCTTTGGCTTTACTAATGAGTATGAATTATCACAGTACTTACTAAAACTTTGCTTTATTTGCCCTATTAAATACATAAGTCTCCCAGGAAAACCTTGATTTATATTCAAGCATTATAAAAGTCCGTGTGAAGCTCTGATCTCTCTCCTGGAGAGTTGAAGCTAGAAGTGACATTCGGCGATGATGTATTTTGTGGTTTTTCTTTGTTTTTAAATCTAAAGAAAAGCCTTGGACATGGATTTAAGATCTTCTACTGAGGATGCAATTATTAGATGTGTGCAATTTGAACTCCATTAAATTATTTTGGATAGCATAAAAATAATTGTTATGAAAATAATTTATGCAATGTCCATGGTTGTCTACTAAAATTAATATGAAATGTAATGATACTGTATACTTGGTCTCTGCAATTATGATTATGTAACTGACTTACAAAATACTTCAAGCAAATATATAAGCTGGCCTTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002056:ENSGALT00000003199:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.222 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF057427=NRDE=FE(12.9=100)
A:
NA
C2:
PF057427=NRDE=PD(12.9=85.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGCAGCTGTGTGTGTTCGTT
R:
GCTTCCAGAGGCTGACAGAAA
Band lengths:
248-357
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]