Special

RnoINT0137300 @ rn6

Intron Retention

Gene
Description
solute carrier family 27 member 4 [Source:RGD Symbol;Acc:1307383]
Coordinates
chr3:8373412-8376858:+
Coord C1 exon
chr3:8373412-8373558
Coord A exon
chr3:8373559-8375897
Coord C2 exon
chr3:8375898-8376858
Length
2339 bp
Sequences
Splice sites
5' ss Seq
CAGGTCTGT
5' ss Score
6.84
3' ss Seq
TTTTCTTCCCCACTCTCTAGGAA
3' ss Score
11.56
Exon sequences
Seq C1 exon
GAGCTGAGGGCCGAGCAGGAATGGCTGCTGTGGCAAGCCCCACTAGCAACTGTGACCTGGAGAGCTTTGCACAGACCTTGAAAAAGGAGCTGCCCCTGTACGCCCGCCCCATCTTCCTCCGCTTCTTGCCTGAGCTGCACAAAACAG
Seq A exon
GTCTGTCCCTGGTTCCAGCCCCTGGCTTTCAGGGCTGGGTCTTTCTGTAGTCTGAGCCCTCTGCCTAATCTCTGACCTTGACAAACAGCCTTGCCCCACGGCTGAGACATTGCTGTCCTGGGTGGATGTGTGCAAGCCTTCAAAGAAGGTTCACCATCCCTTAGCATGATCCTGTACCATGCCTCTGGTACTGTGGTTCCGAAGCACTGGTCTGACTAGGCTTTAGGCTCTCAGAATCTTTTCTCTAGGACCCAGAGGAGAAAAATTCTAAAGAAATTCCAAAGGTATGGAATGGGCTTGGTGTGCTAACACTGTAATCCTGATGCTTCAGAACGGAGGGAGGAGGCCAGCCTTGGCTTTACAGTGCCCAAGACTCTCAGCAGCAGCAAAGCAGATCACGGCACAATAGACTGGGGACAGAACTCAGTGGGAGAGCTTGTCTAACGCACATGAGCGCTTAGGTTTGATTCCCAGTACCACAGAAAAGTAGTAATAAGGAAATAATAAGGCATGCAGGCAAATGGTAGACCAGTAAATTAAAAGGAAGAGAAGAGACCCCCAAACCTGGATGCTTTCAGGGTAGTGTGCTATGGGCCGTCAGCAGAGGCCATCAGGACCAGAAGCCTATAGGATCTATAGGATCTATGGGAGTGGATAGCCTAGAAACAGTAGGAAGCTATCTAAATGTAAGATTGTGTCCTACAGAGGTCTCCAGCTATGAGGTAGACAGTGGCAAAGAACTGTAGATGTCTCAGGAGGAGTTGATGTGTCCAAGAGTGGACTGTGGGTGGGTCTGTGGTCACATGGTAGCACACTGACATCCTTCTAGTATTGGTCTGCTGATGGCTGTCAGGGGTTCCAAGTCAGGGAGGGAGTGTAGAAACTCCTGTCTAGGCCCACCATGCTCTCCTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCATGCTCTCCTTCTTGTCCTCCTTGGCTCTCCCATTGCTCAGTGTCTTCCCTGGCTGCTCCCCTGGGGTCCATGTGCCTGACCCCCTCCCTCCCATGTGTCGTCAGTTCCAAGCCTTGTCTGGCTGCTGAGGTCTGTGTCAGCTCATGGACATCTGTAGCCCATGCAACACATGAAACGGTGGGAGGGGGCTAGGCTCTGGTGTGACATAGGGGGGGACACAGGTGCCAGCCTCACAACTGAGACTGAGCTTCCTGAGGGCTGGCTGTGTGACTCTGCCAGGACAAGCAGGGACAGAGCACTACATGCAAGGGTCTCTGGGGGCCACATTCTGTGGGTTAGTGATGTGGGGTTTGGATTCCACTGTGAGGTGTTGGTGGGGCAGCAGAGGCGATAGCCCCCCTCCTCTGTAGCCCCATCCAGCAAAACTGTGCTGGGAGGGGTGTTCGGCATCTCTGCTGTCCACTGCGGTGGCACTTAGCACCGTGGAGGAATTGAGCATTTGAGATAGAGTTGGTGTGACCGAGGAACTTGCACACGAGCAGTGCTGGTCGAAGGGACTCGTCTGGGTTGGTTTTATGAGAGATAAAGCTGCTCATTCTTCCAAGGCTGGTCTGATCTCTAGGCATCTCTCCCCGCCACCCCACCAAGAGCATGGGGGTGGAATGGCATGGAGGCCTAGAGTCAAGGAATTCCACAGTATTGCTTCAGAGCAAGTTAGAAGGCCAGTCTGGTTTGGGGGAGTGCAGTTTCTGTTGGGAGCAATAGCTGGCATTTCAGAGGTTAGCAGATCCAGGGAGAGGGTCTGTCATTCCCAGGTTCAAATACTGGCTATCACTTGCTTACTGTGTGATGACTTTGGCAAAACAACAACACCAAAAAAACCAAAAACAAAACAAAACAAAAAACAAAAAACCAACAACAACAACAAAAAAAACCCAACAAAACAAACAAACAAAAAAACCCCGTGGTGACTCACCCCCTTAATCCCAGCACTGTAGATCTAAGGACCAGGGGATCTCTGTGGGTTTGAAGGACAGCCAGGACTATCTAGTGAGACCCTGTTCAAAAGGAAAAAAATGAAGAAGGAAAACACATGCATCTTAGAATATGATCGGGCATCTGCCTCAAGATGTTGATGCCTCTGCATCCATTCAGTGCTCAAATAAAAGGGACTCAGATTCTGGCCTCTACGCTGCTGTCCATCAGCGATATCCCTGTGTCCTTTCTCCGCTCCCTAACTCTCCTTTTCTCAGCTCTTGTCATCAGATTTCTAGCTCCAATGCCTGCCTTGCACTTTCTGAATTTTCTTCCCCACTCTCTAG
Seq C2 exon
GAACCTTCAAGTTCCAGAAGACAGAGTTGCGGAAGGAGGGCTTTGACCCGTCTGTTGTGAAAGACCCACTCTTCTATTTGGATGCCCGGACAGGCTGCTATGTTGCACTGGACCAAGAGGCCTATACCCGCATCCAGGCAGGCGAGGAGAAGCTGTGATTTCCCCCACATCCCTCTGAGGGCCAGAGGATGCTGGATTCAGAGCCCCAGCTTCCACCCCAGAGGGGTCCTGGGCAAGGCCAGACCAAAGCTAGCAGGGCCCGCACCTCCACCCCTAGGTGCTGATCCCCCTCTCCCAAACTGCCAAGTGACTGACTCACTGCCGCTTCCCCCACCCTCCAGAGGCTTTCTGTGAAAGTCTCATCCAAGCTGTGTCTTCTGGTCCAGGCGTGGCCCCTGGCTCCAGGCTTACTGACAGGCACCTTTAGGATGATGTCTTGGGTCCAGCGGGCCAGGATGTGGGAGAGGAGTCACTGAGATCCCTCCAAAAAGAAGGGAGCTTACAAATGAACCAAGACAAAAGCCTCTCGACTCAGGAAGCTAAGTGGCCAGAGACTGAAGTGGCCAGCCATCCCGTGTCCACAGAGGATCTTGGTCCAAAGCTGCCAAAGTGTCACCTAGCCCTGTCTGCACCTCTGGGGAAAGGAGGACAGCATGTGGCCAAAGTGTCACTTAGCCCTGTCTGCACCTCTGGGGAAAGGAGGACAGCATGTGGCCACTGGGCCCCTGTCTCAAGAAGTCGGGATCGCACACACACACACACTCCTTGTTTCTCCAGATTCCCTTGTCCTTGTCTTAGGGAGGGAGGGGGGTGTCCTGTCTGTCTCTCAGATGCAGGCTTCCTGCCTGTCTGTGAGTCTGTCCCTGTGTGTTGCCTTCTCCATCTGTCCTAGCCTGACTGTGGGTGGAGAGGGCATGAGGGGAGGCTCAGGGGCTAATAAACTCTGCCTTGACTCCTCTTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000014369:ENSRNOT00000019500:12
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

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

C1:
PF131931=AMP-binding_C=FE(64.5=100)
A:
NA
C2:
PF131931=AMP-binding_C=PD(3.9=5.7)


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:
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]