Special

RnoINT0033697 @ rn6

Intron Retention

Gene
Description
caudal type homeo box 1 [Source:RGD Symbol;Acc:621233]
Coordinates
chr18:56338336-56339185:-
Coord C1 exon
chr18:56339040-56339185
Coord A exon
chr18:56338567-56339039
Coord C2 exon
chr18:56338336-56338566
Length
473 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGT
5' ss Score
9.8
3' ss Seq
AATTCTCTGCAATCCCACAGGTA
3' ss Score
7.97
Exon sequences
Seq C1 exon
GTAAGACTCGGACCAAGGACAAGTACCGCGTGGTCTATACAGACCACCAACGTCTAGAGCTGGAAAAGGAGTTTCACTACAGTCGGTACATCACCATTCGGCGCAAGTCAGAGCTGGCTGCTAACTTGGGTCTCACAGAGCGGCAG
Seq A exon
GTATGTGGGCCCTCCAACTCAGCTCAAGTAGTTGGGCTTTCAGGTTGCCATGCATGGACAGAGCCCACAAAAAAAAATAAAAAAAAGGTAGTCTCCAGACTACTGGCACAAAACCACACACTGAACCACTGCCATACCACCAACTAAACCCAACATTATTCCATACACACAAACAGACATATGTATGTGTGCGCACACACACACACACACACACACACACACACACACACACACACACACAGAGGCTACAGTGGCTGGTGATCAATGCTATTCAAACCCAGAGGATGGGCAGTCACAGAACATGGGGGCTCTGGAGGACTGGGGCCTTGTAGGAGGTTTCAGAGAAGGGTGTCTAGAGCACAGGGAGAATGTATTTTAGTGGTGACTGGAGCAGAAAGTGGATCATGAAGACCACCTCTCCCAGCCCAGCTCCTTCCTAAAATCTGCAGCATAAATTCTCTGCAATCCCACAG
Seq C2 exon
GTAAAGATCTGGTTCCAGAACCGTCGGGCCAAGGAGCGTAAAGTAAACAAGAAGAAACAGCAGCAGCAGCAGCAGCAACAGCAGCAGCCCATGCCTCCCACACAGTTGCCCCTGCCCCTGGATGGCACCCCCACACCATCGGGGCCACCCCTGGGGAGTCTATGCCCCACCAATGCTGGTCTTCTGGGCACCCCCTCCCCAGTGCCGGTCAAGGAGGAGTTTTTACCCTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000060334:ENSRNOT00000083379:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.327 A=NA C2=0.947
Domain overlap (PFAM):

C1:
PF0004624=Homeobox=PU(73.7=85.7),PF119313=DUF3449=PU(44.8=79.6)
A:
NA
C2:
PF0004624=Homeobox=PD(22.8=16.9),PF119313=DUF3449=PD(52.9=59.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAAGGACAAGTACCGCGTGG
R:
AAAAACTCCTCCTTGACCGGC
Band lengths:
357-830
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]