Special

HsaINT0153402 @ hg19

Intron Retention

Gene
ENSG00000114923 | SLC4A3
Description
solute carrier family 4, anion exchanger, member 3 [Source:HGNC Symbol;Acc:11029]
Coordinates
chr2:220501024-220501596:+
Coord C1 exon
chr2:220501024-220501172
Coord A exon
chr2:220501173-220501401
Coord C2 exon
chr2:220501402-220501596
Length
229 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
CCGCTCCTACCCCCACCTAGTTC
3' ss Score
5.54
Exon sequences
Seq C1 exon
GAGAGAAGACCGAGGGGCTGATGGGCGTGTCCGAGCTGATCGTGTCCACCGCTGTGCTCGGCGTCCTCTTCTCTCTGCTGGGAGCTCAGCCGCTGCTTGTGGTTGGCTTCTCTGGGCCGCTGCTTGTGTTTGAGGAAGCCTTCTTCAAG
Seq A exon
GTGAGGCGAAGCCTTGCCCTGCTCCATCCATCCTGCCCCACACTCTTCCTTACCTACATCCTGCCCCACACTCTTCCTTACCTACATCCTGCCCCACACTCTTCCTTACCTAGGGGATGGGTCCCTGCATTCTCCCTCTTCCTCGGAGTTCATCCGCTGCCTATTCCAGGGGGCATTGACACCCAGGGCAGTCCACCTGTGGGTAACGACCGCTCCTACCCCCACCTAG
Seq C2 exon
TTCTGCCGAGCCCAGGACCTGGAGTACCTCACTGGCCGGGTGTGGGTTGGTCTCTGGCTGGTGGTCTTCGTCCTTGCCCTGGTGGCCGCCGAAGGCAGCTTCCTGGTCCGCTACATCTCGCCTTTCACCCAGGAGATCTTTGCCTTTCTCATCTCACTCATTTTCATCTACGAGACCTTCTACAAGCTCTACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000114923-SLC4A3:NM_005070:15
Average complexity
IR-S
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(10.0=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(13.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAGAAGACCGAGGGGCTGAT
R:
AGGCAAAGATCTCCTGGGTGA
Band lengths:
292-521
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains