Special

HsaINT0102271 @ hg38

Intron Retention

Gene
Description
microfibrillar associated protein 4 [Source:HGNC Symbol;Acc:HGNC:7035]
Coordinates
chr17:19386310-19386838:-
Coord C1 exon
chr17:19386760-19386838
Coord A exon
chr17:19386465-19386759
Coord C2 exon
chr17:19386310-19386464
Length
295 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAGC
5' ss Score
9.26
3' ss Seq
CCCCATGTCCCTACCCCCAGCTC
3' ss Score
8.36
Exon sequences
Seq C1 exon
GCACTCCTGGCCCTGCCGCTGCTGCTGCTTCTCTCCACGCCCCCGTGTGCCCCCCAGGTCTCCGGGATCCGAGGAGATG
Seq A exon
GTAAGCAGCCCCACACTCACAGACGCGGCCTGGCCCACAGGTTGTGCAAGAAGAGGCTGGACTGTCAGAACAGACTGTCAGGGCCGAGCCCCAGCTCTGCAGGACTCAGGTTCCTCCTTTACAAAATGGGGCAGATGGATGACATAAGCATTGCTCATCTCCCTTGAAGAAATCTTCCATGACTCCTTGTGTCAAAGTCCCCCAGCCCCAGGGACTGAGGCAAACCTTGGGGTGCTGAGGTGTCAGTGATGCCATAGTCCCACTCTCCTCACTGTCCCCATGTCCCTACCCCCAG
Seq C2 exon
CTCTGGAGAGGTTTTGCCTTCAGCAACCCCTGGACTGTGACGACATCTATGCCCAGGGCTACCAGTCAGACGGCGTGTACCTCATCTACCCCTCGGGCCCCAGTGTGCCTGTGCCCGTCTTCTGTGACATGACCACCGAGGGCGGGAAGTGGACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000166482:ENST00000299610:2
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:
NO
A:
NA
C2:
PF0014713=Fibrinogen_C=PU(19.6=82.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGCTGCTGCTTCTCTCCAC
R:
GTCCACTTCCCGCCCTCG
Band lengths:
215-510
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