Special

HsaINT0153304 @ hg38

Intron Retention

Gene
ENSG00000004939 | SLC4A1
Description
solute carrier family 4 member 1 (Diego blood group) [Source:HGNC Symbol;Acc:HGNC:11027]
Coordinates
chr17:44251159-44251588:-
Coord C1 exon
chr17:44251419-44251588
Coord A exon
chr17:44251333-44251418
Coord C2 exon
chr17:44251159-44251332
Length
86 bp
Sequences
Splice sites
5' ss Seq
CGGGTACAG
5' ss Score
4.22
3' ss Seq
ACCCCAGCCTCCGCCTGCAGGTG
3' ss Score
8.94
Exon sequences
Seq C1 exon
GCCTGTCCATCCTCATGGAGCCCATCCTGTCCCGCATCCCCCTGGCTGTACTGTTTGGCATCTTCCTCTACATGGGGGTCACGTCGCTCAGCGGCATCCAGCTCTTTGACCGCATCTTGCTTCTGTTCAAGCCACCCAAGTATCACCCAGATGTGCCCTACGTCAAGCGG
Seq A exon
GTACAGGACCCTTTTCTGGCTGCCCAGCCTGGGGTGGTAGAGGGTGCTGGGGTGTGATAGGCACTGACCCCAGCCTCCGCCTGCAG
Seq C2 exon
GTGAAGACCTGGCGCATGCACTTATTCACGGGCATCCAGATCATCTGCCTGGCAGTGCTGTGGGTGGTGAAGTCCACGCCGGCCTCCCTGGCCCTGCCCTTCGTCCTCATCCTCACTGTGCCGCTGCGGCGCGTCCTGCTGCCGCTCATCTTCAGGAACGTGGAGCTTCAGTGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000004939:ENST00000262418:18
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(19.7=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=PD(3.9=19.0)


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:
CCTGGCTGTACTGTTTGGCAT
R:
GGATGCCCGTGAATAAGTGCA
Band lengths:
167-253
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains