Special

GgaINT0113148 @ galGal4

Intron Retention

Gene
ENSGALG00000006606 | KIAA1324L
Description
KIAA1324-like [Source:HGNC Symbol;Acc:HGNC:21945]
Coordinates
chr1:7501895-7503263:+
Coord C1 exon
chr1:7501895-7502068
Coord A exon
chr1:7502069-7503073
Coord C2 exon
chr1:7503074-7503263
Length
1005 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGC
5' ss Score
8.7
3' ss Seq
TTTTTCCTGATTGTTTGCAGGGT
3' ss Score
9.25
Exon sequences
Seq C1 exon
GACCACTCCGCCTGCTTCAGTGACTGCTTGGTGTCATACATCAAGGATAACCAGACCCTGAGTTATGATTTTAGCAACCTCAGCCAGGTGGGCTCCTTAATGAGTGGGCCGAGCTTCACTTCCCGTGGGACCAAGTTCTTCCACTTCTTTAACATCAGCCTGTGTGGAAATGAG
Seq A exon
GTGAGCTCAGTGGGTGTTGAGGGTTGAGTTAACCAACGTGTAGTCCATGTTGATGCTTGGTGGGATCGCACTGAGACAGTGTGCATCACTGCTGTGCAAATGCTTTCCTCTGTATCTTGCCCCCAGTCAGATTTGGAGTGTACCAGAGCATATTGTCACATACAAGAATTGACATTTTGGAGCAGTACCAGATGATTATCCCTTGAAAGCCAATGCATGCAGTTTACATCAATGTTTATCCCTGTAAAGTTAGGAAATCTCTTCTCCATATACCAGAGGGTTTGCATGAGATAAGCCAATAGTTGTATTTCTTTAAAGAATTTTGCATACTTTTGGGCTTAAATGTGTGCATACCTATCTGGATTAGAGCTGATGACAGATCCATAAAGATACTCCCCTGTGGATCTGCTCTTCATTTCTCAAACATTTTCCCTGGTACTATCAGACCTAGAGGACCAGGTCTGTGTGCTTGGCATTTTGGAGGGTCAAGACTGCCAAATTTCTTGATTTGGCTTTCATTGCTGCTGTTGTGAGATTCTTACATTAGTCTCAGTTTGTGACATTAATGCGGTCTTGGAGGCTGTGTATCTGCTTATGGATTTAATGTAGTCATGCTTTGAGAATATTTTATCTGGTTTAAATTCCAAATAAAGAGGTATTCTACAGTGCATTATTTACAGGCAATATGTTTTTTCTGTACAAGCCATTTTATTATGCTCTGCAAGTAAGCACTGTGCTGTCAAGATAAACAGAGAAAAGTGCTTCGTAGCACAAGTTTCTGATAAGACCCATACTGGAGGTGACATCTTGTTTCTGAGTCTAAACGAGGCTTTAATCGGAGCCTTCAGAATGACACAGTTTATTGCTGCAATTTGTTTCTCTCATGATAGAAACATGGAGCTATTTCTAAGACGAATGAAGCTCATACAGTTTGCAATGTCTCCCGAACTTTTCCACATCCTATCAACAACCAACAGCTTCCCCATTTTTCCTGATTGTTTGCAG
Seq C2 exon
GGTAAAAAGATGGCTATTTGCACTGACAATATCACAGATGTTACCCTGAAGGACATGGTTGCAGAATCAGAAGATTTTTCCAACTTTGTGGGAGCTTTTGTCTGTCAGTCCACCATCATCCCATCGGACAGCAAGGGCTTCCGAACAGCCCTGGCTCTTCAGTCCAATAGCCTTGCTGACAGGTTCTTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006606:ENSGALT00000010664:15
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:
PF076998=GCC2_GCC3=PD(15.7=13.8)
A:
NA
C2:
NO


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:
TGCTTCAGTGACTGCTTGGTG
R:
ACCTGTCAGCAAGGCTATTGG
Band lengths:
346-1351
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]