Special

GgaINT0011637 @ galGal4

Intron Retention

Gene
Description
solute carrier family 35 member C2 [Source:RefSeq peptide;Acc:NP_001026036]
Coordinates
chr20:11072400-11073745:-
Coord C1 exon
chr20:11073570-11073745
Coord A exon
chr20:11072530-11073569
Coord C2 exon
chr20:11072400-11072529
Length
1040 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
CATGTTTTTTCTTTCCACAGGAA
3' ss Score
12.72
Exon sequences
Seq C1 exon
GCCTGCCTTTGTCCGTATCAGAGAGGCTCTTCCACTTCCATGAAGCAGGAGTGATGTTCTGTATGGTAGGAAAGCTGTTGTTGGGTGGAATTCTTGCCTTTGGTCTAGGCTTTTCTGAGTTCCTCTTGGTTTCCAGAACATCTAGCCTCACCCTTTCTATTGCTGGTATTTTTAAG
Seq A exon
GTAAGGCATGGTTCCTGTTCTAATACTAAAGGGCAAGTACTGGGTCACCCCTAATGGGCCTAATGTGGTGGGAACTTCCTTACAGCCTCAGAAGTCGTCTGTGATTTTTATTCTCCTGACACAGGAGCTTGATGCGTTGACTTGCTGTCTCTGCAGTGAGGGCTCGTAGTCCCTGCTGCTCTGACAACAAAGGGCAGAAGCATTAAATACTGTTAAGGTCCAAAGTTTGGTGGGATCTGGGGGAAACTAGAACACGTGGGCCTCTTGAGCAATGGATGGTGTGGGAGGGAAGAGAGTTAGGAAGAACGCTTTGTTGCATCAGACCTGGATAAGGATAAACCTCTGGTTAGAGGTAACTCATTAACCTGGTTTGGCATGTTCTAAGCAAGAATCACAGAATTGCTCAGGTTGGAAAAGACCTTAAAGATTATCGAGTTCAACCACGACCTAACCAAACTACCCTACCAGCCCTCTGCTAAATCATGTCCCTGAGCACCACATCCAAACCAGGGATGGTGACTCAACCACCTCCCTGGGGAGCCTATTCCAGTGCTAAACGACCCTTTCTGTAAAGAAGTGTTTCCTGATATCCAACCTAAACTTATCCTGGCATAACTTAAGGCCATTTCCCCTCGTCCTTGCTCTCAGCAGCTCTCACTGCTGTCGCCTGTCAGCAGTAAGAAGAGACCAACCCTGCTCTGCTGTAAGCACCTTTCAGATATTAGAAGAGAGCGATAAGGTCTCCCCTCAGCCTCCTTTTCCCCGGGCTAAACAGCCCCAGTTCCTGTCCTTCCTTGACAAGTACAGTGCATGTACTTCTGAGCTGGTTGGTGACATGTGAAACTCAGCTATGTAGGAATCCTAAAACTTCCAGATTAGATGAGTGGTTCAATCAGGGGACGTAAAATCCCCGATCCCAGTTTGACAGGTTGTTCTGATTCTGCAGCCTGACATCTTGATTTAGGCTTCAGCTGCAAAATAACTTACTCACACCTCGTCAGGTCCTGTGCTGCCACTTGTCATGTTTTTTCTTTCCACAG
Seq C2 exon
GAAATCTGTGTTTTATTTCTTGCCACACACCTGCTGGGAGACCGCCTCAGTCCCTTAAACTGGCTTGGCTTTGCTGTCTGTCTGTCAGGAATCTCCCTTCATGTCATTCTCAAAGCTGTAAATTCCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000020939:ENSGALT00000039096:11
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:
PF0315111=TPT=FE(38.4=100)
A:
NA
C2:
PF0315111=TPT=PD(23.2=79.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GCCTGCCTTTGTCCGTATCAG
R:
TGGAATTTACAGCTTTGAGAATGACA
Band lengths:
303-1343
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]