HsaINT0076826 @ hg19
Intron Retention
Gene
ENSG00000180448 | HMHA1
Description
histocompatibility (minor) HA-1 [Source:HGNC Symbol;Acc:17102]
Coordinates
chr19:1077856-1079839:+
Coord C1 exon
chr19:1077856-1078044
Coord A exon
chr19:1078045-1079701
Coord C2 exon
chr19:1079702-1079839
Length
1657 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
GCGCCCCGCCCCCACCGCAGGCG
3' ss Score
7.47
Exon sequences
Seq C1 exon
CAAGAGGCGGAGTCCAACCTGCGCAAGGCCAAGCAGGGTTACGTGCAGCGCTGCGAGGACCACGACAAGGCTCGCTTCCTCGTGGCCAAGGCGGAGGAGGAGCAGGCTGGCAGCGCGCCGGGAGCAGGCAGCACGGCCACCAAGACCCTGGACAAGCGGCGGCGGCTGGAGGAGGAGGCCAAGAACAAG
Seq A exon
GTGAGGGCGGGTGGAGGCAGGGCTGGAGGTCCCTGGAGGAGGAGATCCAATGCTTGGTGTGACATTTACTACCTCCAGACCTTTGTTTTTGTTTTTTTGTTTTTTTGTTTGTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGTCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGCGCCCGGCCAATTTGTTTTTTGGAGACAGAGTCTCATTCTGTTGCCCAGGCTGGAGTGCAGTGGTGAGATCTCACTGCAACCTCCGCCTCCCAGGTTCACACAGTTCTCTGCCTCAGCCACCCTGCCACCAAGCCCAGCTAATTTTTTTGTATTTTTAGTAGACACAGAGTTTCACCATCTTGGCCAGGTTGGTCTCAAACTCCTGACCTCATGATCCACCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCCGATTTTTAAATTATTATTATTTTTGAGACAGTGTCTTGTTCTGTCACCCAGGCTGGAGTGCAGTGACGTGATCATGGCTCACTGCAGCCTCTACCTCCTGGGCTCAAGCAATCTTCTCGCCTCAGCCTCTAGAGTAGCTGGGACCACAGGCGTGTGCCGCCACACCCAGCTAATTTAAAAAAATTCTTGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACAAGGTCAGGAGATCAAGACCATCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTAGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAAAATGGCATGAACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAACGAGACTCTGTCTCAAAAAAAAAAAAAAATTCTTTATAAAGATGGGGGTCTCAGGCTGAGTGTGGTGGCTCACACCTGTAATCCCAGCCCTTTGGGAGGCTGAGACGGGCAGATCATATGAGGCCAGGAGTTCGAAACCAGCCTGGGCAACATGGTGAAACCCCTGTATCTCTACTAAAATTACAAAAAATTAACCGGGTATGGTGGGTGGGGGGCACCTGTAATCCGTTACTTGGGAGGCTGAGGCAGAATTGCTTGAACCCGGTAGGTGGAGGTTGCAGTGAGCTGAGATCGTACCACTGCACTCCAGCCTGGCCTACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAGATGGGGAGGGTCTCACCATGTTGCTCAGGCTGGTCTCGAACTCCTGGCCTCAAGCAAGTCTCCCACTGTGGCCTCCCGAGGCGCTGGGATGACAGGCGTCAGCCCCGCCTCCCTGAGGTTTCTGTCTGAGTCCTGCACCCCGGGCTGAGGCCTCTCTCTGTGCGCCCCGCCCCCACCGCAG
Seq C2 exon
GCGGAGGAAGCTATGGCCACCTACCGCACCTGCGTGGCCGACGCGAAGACGCAGAAGCAGGAGCTGGAGGATACCAAGGTGACGGCGCTGCGGCAGATCCAGGAGGTCATCCGGCAGAGCGACCAAACCATCAAGTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000180448-HMHA1:NM_012292:11
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.794 A=NA C2=0.413
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AAGAGGCGGAGTCCAACCTG
R:
CGACTTGATGGTTTGGTCGCT
Band lengths:
326-1983
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)