Special

HsaINT0082938 @ hg19

Intron Retention

Gene
Description
integrin, beta 7 [Source:HGNC Symbol;Acc:6162]
Coordinates
chr12:53587492-53588128:-
Coord C1 exon
chr12:53587982-53588128
Coord A exon
chr12:53587686-53587981
Coord C2 exon
chr12:53587492-53587685
Length
296 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGA
5' ss Score
8.94
3' ss Seq
TGATTCCTGCCTCTTCTCAGGTG
3' ss Score
9.69
Exon sequences
Seq C1 exon
AGCCTGTCTTCCACCGTGACCCTTGAACACTCTTCACTCCCTCCTGGGGTCCACATTTCTTACGAATCCCAGTGTGAGGGTCCTGAGAAGAGGGAGGGTAAGGCTGAGGATCGAGGACAGTGCAACCACGTCCGAATCAACCAGACG
Seq A exon
GTGAGAGCCAGCAAGCACAGGCAGAAGGCGGGCAGGGGGAGGTGGGAGTGGGAAATTAAGCAGGCAGGAAAAGATGGGTGGCAGGTACAGGGAGTGACATGAGAGCCTGAGGTAGTCCTCCATCCATCCTTCCTGGAGCAGTCTGAGTGGCTTCCTCAGGCATGTTTCTAGGAGTTGGGTGTTAACATGACCCCATCCCTTCATTTACTAAGGGGTGAGGTTCTGGATGATTGGTGAGTTTGGGGTATGTGTGTGTGCATGTGTATAACCATGGCCTGATTCCTGCCTCTTCTCAG
Seq C2 exon
GTGACTTTCTGGGTTTCTCTCCAAGCCACCCACTGCCTCCCAGAGCCCCATCTCCTGAGGCTCCGGGCCCTTGGCTTCTCAGAGGAGCTGATTGTGGAGTTGCACACGCTGTGTGACTGTAATTGCAGTGACACCCAGCCCCAGGCTCCCCACTGCAGTGATGGCCAGGGACACCTACAATGTGGTGTATGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000139626-ITGB7:NM_000889:10
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.265 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0036213=Integrin_beta=FE(11.2=100)
A:
NA
C2:
PF0036213=Integrin_beta=PD(9.1=60.0),PF079657=Integrin_B_tail=PU(5.0=6.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACACTCTTCACTCCCTCCTGG
R:
CACATTGTAGGTGTCCCTGGC
Band lengths:
305-601
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development