Special

HsaINT0076827 @ hg19

Intron Retention

Gene
Description
histocompatibility (minor) HA-1 [Source:HGNC Symbol;Acc:17102]
Coordinates
chr19:1079702-1080117:+
Coord C1 exon
chr19:1079702-1079839
Coord A exon
chr19:1079840-1079926
Coord C2 exon
chr19:1079927-1080117
Length
87 bp
Sequences
Splice sites
5' ss Seq
TCGGTGCGT
5' ss Score
8.67
3' ss Seq
CTCTCCGGTGCCGCCCGCAGGCC
3' ss Score
10.74
Exon sequences
Seq C1 exon
GCGGAGGAAGCTATGGCCACCTACCGCACCTGCGTGGCCGACGCGAAGACGCAGAAGCAGGAGCTGGAGGATACCAAGGTGACGGCGCTGCGGCAGATCCAGGAGGTCATCCGGCAGAGCGACCAAACCATCAAGTCG
Seq A exon
GTGCGTGGGGTGCTCCGGCCGCCCGGGCGGGGATGGTGGACCGGGCGGCCTCCTCCTGACCCCTCCGCTCTCCGGTGCCGCCCGCAG
Seq C2 exon
GCCACGATCTCCTACTACCAGATGATGCATATGCAGACGGCGCCGCTGCCCGTGCACTTCCAGATGCTGTGTGAGAGCAGCAAGCTGTATGACCCAGGCCAGCAGTACGCCTCCCACGTGCGCCAGCTGCAGCGGGACCAGGAGCCCGATGTGCACTACGACTTTGAGCCCCACGTCTCCGCCAACGCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000180448-HMHA1:NM_012292:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.413 A=NA C2=0.484
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGAGCTGGAGGATACCAAGGT
R:
CCTGGGTCATACAGCTTGCTG
Band lengths:
177-264
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development