Special

RnoINT0088575 @ rn6

Intron Retention

Gene
Description
MAM domain containing 4 [Source:RGD Symbol;Acc:708583]
Coordinates
chr3:2791086-2791763:-
Coord C1 exon
chr3:2791590-2791763
Coord A exon
chr3:2791171-2791589
Coord C2 exon
chr3:2791086-2791170
Length
419 bp
Sequences
Splice sites
5' ss Seq
CGGGTGAGG
5' ss Score
8.48
3' ss Seq
CTAACCCTCCCTGCCCTCAGATC
3' ss Score
11.06
Exon sequences
Seq C1 exon
TTCACCTTCTATTACTACCTGCATGGGTCTGAGGCCAACCAATTCCAGCTCTTTGTGCAGGCACAGGGGCTCAACACCACCCAGCCTCCTGTCCTACTCCGAAGCCGCCATGGAGAGTTGGGGACAGCCTGGGTCAGAGACCGGGTTAACATTCAAAGTGCCCATCCATTTCGG
Seq A exon
GTGAGGCTGGGCTAGAGGGCAGAATCCAGGGAATCCTGCCTAGAGCACGCACAGGAGTACTCTGGGATTCTTTTTTTTTTTTAAAGATTTATTTATTTATTATATATAAGTACACTGTAGCTGTCTTCAGACACATGAGAAGAGGGCATCAGATCTCATTACGGATGGTTGTAAGCCACCATGTGGTTGCTGGGAATTGAACTCAGGACCTCTGGAAGAGCAGTCAGTGCTCTTAACCACTGAGCCATTCCTCCAGCCCGTACTCTGGGATTCTTTAGTCATTCCTGAAGACTGCTCAGTGGGAAAGCTTGAGAGTGTTGGGAAATTCATGAAGTCTAACAATATAGGGATGGGAAGGGTGCCAGAGGAAAGACAGGACAGAACAGTGCTTGGCATTCCCTAACCCTCCCTGCCCTCAG
Seq C2 exon
ATCCTTCTTGCTGGGGAGACTGGTCCAGGAGGCTTCGTGGGCCTAGACGACCTTATCATGTCCAACCACTGCATACTTGTTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000016584:ENSRNOT00000022390:10
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:
PF0062918=MAM=FE(36.8=100)
A:
NA
C2:
PF0062918=MAM=PD(16.1=86.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg38)
No conservation detected
Mouse
(mm10)
No conservation detected
Chicken
(galGal4)
ALTERNATIVE
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACCTTCTATTACTACCTGCATGGGT
R:
GGAACAAGTATGCAGTGGTTGGA
Band lengths:
254-673
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]