Special

HsaEX6066565 @ hg19

Exon Skipping

Gene
ENSG00000050438 | SLC4A8
Description
solute carrier family 4, sodium bicarbonate cotransporter, member 8 [Source:HGNC Symbol;Acc:11034]
Coordinates
chr12:51897813-51902980:+
Coord C1 exon
chr12:51897813-51897904
Coord A exon
chr12:51899619-51899714
Coord C2 exon
chr12:51901210-51902980
Length
96 bp
Sequences
Splice sites
3' ss Seq
GTCCTAATGATTGATTTCAGATG
3' ss Score
6.13
5' ss Seq
GAGGTAAAG
5' ss Score
8.27
Exon sequences
Seq C1 exon
GAGGCTGAGAAAATGTTAGAAATTGGGGGAGACAAGTTTCCCTTAGAGAGCAGGAAGTTACTAAGTAGTCCTGGAAAGAACATCAGTTGCAG
Seq A exon
ATGTGACCCCTCTGAGATTAATATATCTGATGAAATGCCTAAAACTACAGTTTGGAAAGCTCTCAGTATGAATTCTGGAAATGCAAAGGAAAAGAG
Seq C2 exon
TCTCTTCAACTAAGAGTCTTTGCTGGGATGGAAGATTTGGGCCGTGTGGTGCCTCAGGGAAGTTCTGGTTACAGAGAAAATGGCGAGTCTCTCAGAGAAGAAGCAAGACCAAGTCTGGCCCTGTCCTTGGTCATCTCAAAGCCATGCCGAAGCATTCAGTTATTCTTGGTGTGCATTGGAAGGCATCCAGCTATCCCCATACCAGCAGCCAGTCACCAGATGTGAATGTGGAAGCAGAAGACCACCTCCTGTTGGTTCTTCTCCTCTTCCTTCTTTTTCTCTTTAGAACGGCCACCATTGAAGACCTAGCTTCCCATTTTCCAGACGTTTTCTCTGAAATTCTCTGCTGGCCTGCCAAGCCATATGGATTCATTCTGCCACTGAGGAGTCCTTCAGTGAGGTCCCTCTTCCTAAAGGACAGAGTGGGGAGTAGGAGGGGAACAGAGAGGACATCCTCTCTGGCTCTCCAGTGCTCTTAGTGTCTACAGGCTCCTAGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000050438-'28-28,'28-27,29-28=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.065 A=0.121 C2=0.750
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TCCTGGAAAGAACATCAGTTGCA
R:
TCGGCATGGCTTTGAGATGAC
Band lengths:
174-270
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains