HsaINT0098700 @ hg38
Intron Retention
Gene
ENSG00000177239 | MAN1B1
Description
mannosidase alpha class 1B member 1 [Source:HGNC Symbol;Acc:HGNC:6823]
Coordinates
chr9:137101005-137101672:+
Coord C1 exon
chr9:137101005-137101153
Coord A exon
chr9:137101154-137101483
Coord C2 exon
chr9:137101484-137101672
Length
330 bp
Sequences
Splice sites
5' ss Seq
GCTGTAAGT
5' ss Score
8.56
3' ss Seq
CTACTCTGCTCATATACCAGGAG
3' ss Score
5.54
Exon sequences
Seq C1 exon
AATTTGAGGAAGCCAGGAAGTGGGTGTCGAAGAAGTTACACTTTGAAAAGGACGTGGACGTCAACCTGTTTGAGAGCACGATCCGCATCCTGGGGGGGCTCCTGAGTGCCTACCACCTGTCTGGGGACAGCCTCTTCCTGAGGAAAGCT
Seq A exon
GTAAGTGTCTTGGGGTGTCCTGCAGGGAGATGGTGGACTCGCATTCAAGCAGTTACCCCTTTAGTGGACTTGTGGGGACGTGACTGTCTTCCTGTTTCCTCTTCAAATGCACTGGAGTCTGTTTCTGAGCTCATATTCGTGAGCTGATGAAGCCACTTTGATCACCACTGGCCTTGTAGAGACATTCACTCAGTGCAGAGTGATGCCCGTTTCCTTGCTGCTGTGTTGACCCCAGAGAGCCTTCAGTGTCTCCACTGAACTGCATGAAAGGGTGTAGACGAGGCCTCTGGGTGACCTGAACGTTGGTTCTCTACTCTGCTCATATACCAG
Seq C2 exon
GAGGATTTTGGAAATCGGCTAATGCCTGCCTTCAGAACACCATCCAAGATTCCTTACTCGGATGTGAACATCGGTACTGGAGTTGCCCACCCGCCACGGTGGACCTCCGACAGCACTGTGGCCGAGGTGACCAGCATTCAGCTGGAGTTCCGGGAGCTCTCCCGTCTCACAGGGGATAAGAAGTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177239:ENST00000474902:5
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=0.000
Domain overlap (PFAM):
C1:
PF0153215=Glyco_hydro_47=FE(11.1=100)
A:
NA
C2:
PF0153215=Glyco_hydro_47=FE(14.1=100)
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:
AATTTGAGGAAGCCAGGAAGTG
R:
AACTTCTTATCCCCTGTGAGACG
Band lengths:
334-664
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