Special

RnoINT0138574 @ rn6

Intron Retention

Gene
Description
solute carrier family 4 member 8 [Source:RGD Symbol;Acc:735164]
Coordinates
chr7:142450397-142453540:+
Coord C1 exon
chr7:142450397-142450510
Coord A exon
chr7:142450511-142453378
Coord C2 exon
chr7:142453379-142453540
Length
2868 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGT
5' ss Score
11
3' ss Seq
ACGCTTGTTTTCTCTCCCAGCCA
3' ss Score
8.14
Exon sequences
Seq C1 exon
GTTCGCTCCACGGTGAGTGACTTCGCTGTGTTCCTCACCATCTTTACTATGGTGATCCTAGACTTTCTGATTGGCGTCCCCTCGCCCAAGCTTCAGGTCCCCAGCGTGTTCAAG
Seq A exon
GTAAGTGGACCTCGGGGAGCTTCGCGCCTGAGTGCGCACTGATCTCGAGTTGCCCTCAGAGGCTCAGTAAGCAAAATGTAACGTTTGTTACCAGGAAAAGTTGTCCTACTAAGTCTTAGGAGAATGGAAAGTGACTTAAGGCTGTGCTGGCATGGAGAGGCTTCCACGGAGGGAGCCCGGCTGATACCAGCTGCGCAGAGCTGTGGCTTTAGGGACTGGGAAGGTGTAGAAATGATCTCAGACCTCGGAAGGTCTTGTTGGGGGCCTGCGACTGCTCCTGAATCACCAGGAGATTTCTTCAACACTGTTTTGTGTTTGCTTGTCAGATTCTTGGTAATCCACAGCAGTTAAAAATCTTACATACAAACTGAAATACTGATGAATCCCTGGGATCCCAGTCTAATCCAGTGTGAGCGAGCGAGTGAGCGAGCGAGCGTTCCATGAGGCTGGAAAGTGAGCTCAGTCCCACAGACCCTCACTGGGTGGAGAGGCCAGAAAGCCTGGGCCCGCCCAACCGCCTCAGAAGACACCAGAAGGTGACGGTGTATGGACATTTTTGAGAATTCTGGAATTTCGGTTTCTTTTAAAAAACGCAGAAACAATCCTAAGAGTGTGCTTTTGTTTTGAGCCCCAAGTGCGGGATGCGGGGCTGCTTCGGACTGTCCGCAGCAGCTGACATGATTTACCTTGTGAGCTAGCAGAAGCATGGTTTTGCCAGCTGCCGACAGTTTCTGTGATTGTGTGATGTTTGGAATTCTGGGAACTTCTCAAATTGTACATAATTTTGAGAGCCCCAAGAGGCCAGTGAGTGGTGGTTGGTCATTTAGGGACGGTTGGTTGAGGTTTGTTAGTAGCCGTGGTGAAAGAAGAAACAAAAAGAAAGGGATGAGGCCCAGGATCTCCCCCCCCCCCTGCTCCCCCCCACGCTCTCCCCTCTGTCCTTGTTCCTTTCCTCTCTAGTGTTAGGGGTGAAACTGGGGGGATAAAGGGTGGGGAAAGAGAGGAACCTGCAAAGCAGAAAAGACCAGCTACAGGAAGAGTTCAGGGTGGCAGGAAGACAGAGAGTGGTAGAGGCAGTCCTTGACGCTCCATGGCGCACACCTTTAGACCCAACACACAGGAGGCAGGGGCAGGCAGATCTTTGTGAACCTGATGCCAGCCTGGTCTACAGAGCAGGTTCTGGGCCAGCCAGGGCTTCTCCACAGTGAGGCACTTTACCGTCTTTCTCACCATCTTCACAGCGATTACACAAACTATTAGTATATTTTTTTCTATTTTGTCTGTTTAATTCTGTTGAACTTATTAAAATGCGGAATGGGTTAAGAAACACCATCCACATAACAGCTCAGAGCCCCGTGTCTAGCCCTGTGTCAATGAACACCATACCTGGCTAACTGCAGGACAAAGGAAATAGGTGAGTTTTGAGCATTGGGTTCTTGGGGAAGTCCTGTGATGTGTGGTGAGCTTGAGATGTGAGTTGATTTCTGGGACTTCTGGGAGGCAGGGAGAGACAAGACTGAGAAACAGGAGGTTAAAGAAAATGTGGCTCCTGAAGCAGAGGGAGCTGTCTCCTGTCTTTCTCGGGAAGCAGCCAGTTTGCAGTTCCCTCAGCCAGTCTCCGTAGCCACAGTGGGTAGCTCCCTGACCCAGGGTTCCGATTCTCCACCCTAGAAAGGAAAAGTCGTATTTGCATGCAGGCTGTTTGCAAGCCCCTCCTCTGTGCTTTAAACCATGTCCAGACTGTTTATAATACCTACAGCAACGTAGATGGTGTCTGTTGTACCCTGTAGTGTTTGGAGAACAGTGACAACATCTGTATGTGTCTAACAGAGGTGTCTCCACAAGAATCTTTTGTCTGTAGTTCATGGGCTTGGCTATGACTACTTATAACATTGTTAATGGTTTAGTACGTTTTGTGTTGGTCTGAGAACATAACTACTACCTGTAGTACTCTTACTACAGAAGCATAAGTTCTAAAGCTTTTAAAATGTATTCAACCATTCAAAAGCCAGGACATGCCAGTATCATTTGAAACCAAGTATTGTAACTAAGTATCAACAAGATGTAGCAAGCTTTCCTTTGTTTGCTGAGTTTTCCGGTCATTCTGGGTGATAATACTTTTATCCTCCAGCACCGAGTGTTTTCTCCAGAGTGCACCGAGGGAGGGGTCAAGAGTTTGAGCAAATGACTTATAAAGTCATTGAAGAAAGATGGTCCTAGATCAGTTCCCTAAGCTTTGGGCCTCCTGACATCTTCAGTTCCTGGGCTTCTGTTTCACCACTGATGAGAGGAGCTCATGGGACAATCTACTCTCAGCCCAAGAACTATGAGTCTGTCTTTCTTCTGTACTTCAGACGGAGAGTCCATGGCTTGCGGAGAGGAGGGGCGAGGGTTAGCTGTATTATTTAGTCTTCAGAAGGCAATTTTTTTTTGTTGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCCAGAAGGCAATTTTTAAATAACAGATAAGTTGCTAATTATGCTGTACTTGTGGTGAGGTCGAGATGAAGTTGCTTTCTCTGTTCTTGGGGAATAAACAGAAGGCAGTGAGGATTAATGCGAAGTCCGCAGGAAGCTGATTAGTAAGGACTGATGGCCAAAGGAGATCTGGAAAAAAGGTCCAGGGACTTCCTTAGGGGCTGCTATAGTTCATACTTTGTTTTGTTTTTCTAAAGTCTTTCTCCTTCAAAGGAGAACAAAGAGACACGTGGAATAATGTTCAGTGTGGTTTGGTTTGCGCTCCTCTTCAGAGTTAAGATACAGAAACCACGCTTGTTTTCTCTCCCAG
Seq C2 exon
CCAACGAGGGATGATCGAGGATGGTTCATTAGTCCCATCGGCCCCAATCCCTGGTGGACCGTGATAGCCGCGATTATCCCAGCTCTCCTGTGCACCATCTTGATATTCATGGACCAGCAGATCACCGCCGTCATCATTAACCGGAAGGAGCACAAGCTCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028879:ENSRNOT00000040890:17
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:
PF0095516=HCO3_cotransp=FE(15.2=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(10.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
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]