Special

HsaINT1007843 @ hg38

Intron Retention

Gene
Description
chloride intracellular channel 1 [Source:HGNC Symbol;Acc:HGNC:2062]
Coordinates
chr6:31733836-31734263:-
Coord C1 exon
chr6:31734154-31734263
Coord A exon
chr6:31733962-31734153
Coord C2 exon
chr6:31733836-31733961
Length
192 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGC
5' ss Score
10.08
3' ss Seq
ATTCCTGATCCTTTCTCCAGGCG
3' ss Score
9.35
Exon sequences
Seq C1 exon
GCTGGCAGTGATGGGGCCAAGATTGGGAACTGCCCATTCTCCCAGAGACTGTTCATGGTACTGTGGCTCAAGGGAGTCACCTTCAATGTTACCACCGTTGACACCAAAAG
Seq A exon
GTAGGCCTGCTTATGTTCCTTGAAACACCCCTGGTGTACACATGTGTGCAAACACACACCCACCCGAGTCCTTCTGTCATGAACATTTTTGCCCTCCCCCTGGAGTCCCTTTCTTATCCCACGTCCTCCATTCCCCCTTTCTGGTTCTTCCTGACCCCCATTTCCAGTCCTGATTCCTGATCCTTTCTCCAG
Seq C2 exon
GCGGACCGAGACAGTGCAGAAGCTGTGCCCAGGGGGGCAGCTCCCATTCCTGCTGTATGGCACTGAAGTGCACACAGACACCAACAAGATTGAGGAATTTCTGGAGGCAGTGCTGTGCCCTCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000213719:ENST00000375784:2
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=0.023
Domain overlap (PFAM):

C1:
PF134171=GST_N_3=PU(40.8=78.4)
A:
NA
C2:
PF134171=GST_N_3=PD(57.7=95.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCAGTGATGGGGCCAAGATTG
R:
CTGGGAGGGCACAGCACTG
Band lengths:
232-424
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains