MmuINT0078132 @ mm9
Intron Retention
Gene
ENSMUSG00000066842 | Hmcn1
Description
hemicentin 1 [Source:MGI Symbol;Acc:MGI:2685047]
Coordinates
chr1:152548962-152550475:-
Coord C1 exon
chr1:152550299-152550475
Coord A exon
chr1:152549114-152550298
Coord C2 exon
chr1:152548962-152549113
Length
1185 bp
Sequences
Splice sites
5' ss Seq
ATGGTACGC
5' ss Score
8.57
3' ss Seq
CCCACCTTGTTTTTTTTCAGTGC
3' ss Score
10.37
Exon sequences
Seq C1 exon
TTATCACGTGGTACAAAGACAGCCATCCCCTCTCAGGCTCTGCAAGTGCAGCCTTCCTGAAGAGAGGCCAGGTCCTTGAGATTGGGAGTGCTCAGATCTCAGATGCTGGCATCTACAAATGTGTAGCCATCAACTCTGCTGGAGCTACAGAACTGTTTTACAGCCTACAAGTTCATG
Seq A exon
GTACGCGCTACATCTCTCAGGTTCATAATGGGTGATAGTCACGTGGACAATGACCGTATGCCTTTATCAAATTATAATGTGATTAATAAACAGAACTATGCTATTGATATTTTTACTTAAAGAGCCAGTGCTCTGAAACTGGTAAGCTTTCCTACTCCTGACATCTACTAAAATGCCCAGTTCTCACACACTGTTGATTACTTTAGATCACTTGCTAAAATAACTAGTGATGGCTTTGCCAGCTAATAACAATACTACCTTTATTAATGCAACTCTAACACTCATGGATATTAAAGAAATGATTTTAAGAGACATTGACAATTAGAATATGACAACATATGAAATGGAGAAAGGTATGTGTGTACACACTCTCTCTCCCTCCCCCTCCCCCTTCCCCCTCCCCCCTCTTCCCCCCTCCTCCTCTTCCCCCTTCTCTCTCTGGAATCAATAATCCACTCAGGGCCATTGAGATAGCTCAACAGATGTAAGCACTCTCTGAACTTGGGTGAAAGGGCTGATGTGGCAGCAGCCACTTGTCATCCCAGTACTCCTATGCCAAGGTGGATGCTGGCAATAGGGTTTCTCTGAAGCTCAAGGGCCAGTGAGCATGGAGTCCACAGCCTGGCAGAAACAAGAGGAAACCTGACCCAACAAGGTAGAAGAAAAGAACAGACTTCCCCGAATTGTCCTTTCACCTTCACAGGTACATGCACACATGCATACACACAATAATAATAATCTAAAATTCAAATGTACTACGACACTAAAAACTGACTTCTTAAAATAACTAGCAACACTTATTTATCCTCCTCTGCCAAGCTGAGACACTGGTACTTGCCCTACATAACTCACAGGATTACTGTGATTAGATGTCAGATTAGACGTGAAACACTTGGCCAAAATAACAAGGAAAAATTACCTTGTAAAAATTATTATGGAGCCGGGCGGTGGTGGCGCACGCCTTTGATCCCAGCACTTGGGAGGCAGAGGCAGGCGGATTTCTGAGTTCGAGGCCAGCCTGGTCTACAGAGTGAGTTCCAGGATGGCCAGGACTATATAGAGAAACCCTGTCTCGAAAAACCAAAAAAAAAAAAAAAATTATTATGGAAATTGCATATGGTTTTTCATTGTCCTGTGGTGACAACAGACATTACTGTTTGTTCCCCCCACCTTGTTTTTTTTCAG
Seq C2 exon
TGCCTCCTTCGATCTCAGGTAGCAGTTCCATGGTGGAGGTGGTGGTGAATAATCTAGCAAGGTTAGAATGTGAAGCCAGAGGCATCCCTGCCCCGAGTCTGACCTGGCTGAAAGATGGGAGCCCAGTCTCTAGCTTCTCTAATGGAATACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000066842-Hmcn1:NM_001024720:38
Average complexity
IR-S
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:
PF0767911=I-set=PD(67.1=95.0)
A:
NA
C2:
PF0767911=I-set=PU(53.9=94.1)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TCACGTGGTACAAAGACAGCC
R:
CTGTATTCCATTAGAGAAGCTAGAGA
Band lengths:
326-1511
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Pre-implantation embryo development
- Muscular differentiation time course
- Spermatogenesis cell types
- Reprogramming of fibroblasts to iPSCs
- Hematopoietic precursors and cell types
Other AS DBs: