Special

MmuINT0147280 @ mm10

Intron Retention

Gene
Description
solute carrier family 4, sodium bicarbonate cotransporter, member 9 [Source:MGI Symbol;Acc:MGI:2443384]
Coordinates
chr18:36533889-36535443:+
Coord C1 exon
chr18:36533889-36534002
Coord A exon
chr18:36534003-36535281
Coord C2 exon
chr18:36535282-36535443
Length
1279 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGA
5' ss Score
8.68
3' ss Seq
CTCATGGAATATCCCCTCAGCCT
3' ss Score
2.08
Exon sequences
Seq C1 exon
GTGCGCAAGGTGTTGGGCGACTTTTCCTCAGTCCTGGCCATCCTGCTGGGCTGTGGCCTTGACACCTTCCTGGGCCTAGCCACACCGAAGCTCTTGGTGCCCACAGAATTCAAG
Seq A exon
GTGAGAGTCGGACAGGATGAGAAGGGGAAGAGGAAGTGGGGCCAGAAACTTGGAGTAGTAAGACGATTCATATATCCCAAACTTCTTTCCCTCTGAGCTTCTTCCGCCACTCATGAGAGAGCCAGTAACAATGGCCTCACAGAGTCTCTGAGTGATAAAATGAGGTATTTCAACAGACACATCCATAAATGAGGAATGCTGTACACAGTGGCAATTATTATAGGGTAGGTGTTGGAGGGCAGGCTCCAGGCAGCAGGTCTTGCTCTAGGCATCTCCTTTCTAAAAGGCAGAGTGTCACAGTAGTTCAGGTTAACCTCAAACTCCAAACACAGCTGAGGGTGGCCTCGAACTCATCATCATCCTGCTTTAACCCCTCATGCGCTGTAGTTACAGACGTGCATCACCATACCTCTCCTGAGACTATCTTAGTCTTTAAAATGGAATAATCAATAGCAGTTCTCCCATAGGTTTTTTTGGGGGGGTTACATATCATAGTGTAAATAGTTACTACAGTGCCTGGCACATTCCACATATGAGTAACTGCGCTGTCACTGCTTCTCCCTGCCACTGGGCCTACCTTCTTCCCCGCACCCTACTCTTCTTTACGCTCCTCACTACCAGCTCGGATACAGTAAAGCTGGAGCTCCTACTGTGGGGCAGAACAGCAATGGGGGCTCTCCAGGGGTGGCTTTAGAGCTCAGAACCCCAGCCAACCACTCGGGCCCCCTCCGCACCACAGACGCTTATAAATCAGAGCAGACACAGACACACCTAGCCCGGCCCCAGTCTGAGGCAGGTCTGAACCTGAGCTGCCCCAGACTGGGTGTGGGGGCAGGGAGGGGGAGCCTAAGGAGGAAGGCTCTGAATAAGTACAAAGCAGTGTGTGCTGGTTTAATTCACCAACTCGGCTTCCCCGGCGGGGGGAGGGGGGAAAGAGAGAGAGAGAGACAGACAGACAGAGAGACAGAGAGAAGAGACAGAGACAGAGAGAGTTCTCCCTACCACCACCACCAAAGTCCAGAGTCCTTCTTTCTGCTCTCTTTTAAGGCACTGGTATACACTGAAGGAGAGTAGTGTGTGTGTCTCTATGTGTCTCTGTGAGAGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTATGAGACAGTGCTCTCACCTAGAATCCAAGGTCTTGGGGGCAGGGTGTGGAATGTGGTAGACTGTGATAGTGGTAGAGGTGTGCTGTCGAGGTGTTCCTGGGAGACATTTCCACCCTGCTCATGGAATATCCCCTCAG
Seq C2 exon
CCTACACTCTCTGGGCGTGGCTGGCTGGTGTCTCCTTTTGGAGCTAACCCCTGGTGGCTGAGTGTGGCCGCTGCCTTGCCCGCTCTACTGCTGTCAATCCTTATCTTCATGGACCAGCAGATCACGGCAGTCATCCTCAACCGTGCAGAATACAGACTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000024485:ENSMUST00000074298:13
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(8.8=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(12.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CGCAAGGTGTTGGGCGAC
R:
CAGTCTGTATTCTGCACGGTTGA
Band lengths:
270-1549
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • Ribosome-engaged transcriptomes of neuronal types
  • Neural differentiation time course
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types