Special

RnoINT0012770 @ rn6

Intron Retention

Gene
Description
activin A receptor type 1B [Source:RGD Symbol;Acc:735207]
Coordinates
chr7:142848566-142849976:+
Coord C1 exon
chr7:142848566-142848722
Coord A exon
chr7:142848723-142849851
Coord C2 exon
chr7:142849852-142849976
Length
1129 bp
Sequences
Splice sites
5' ss Seq
ACGGTAAGT
5' ss Score
11.81
3' ss Seq
AACTCTTTCTTCCATTCCAGATA
3' ss Score
10.69
Exon sequences
Seq C1 exon
GGAAGCCTGGAATTGCTCATCGAGACTTGAAGTCAAAGAACATTCTGGTGAAGAAGAATGGCATGTGTGCCATTGCAGACCTGGGCCTAGCTGTCCGTCACGATGCTGTCACTGACACCATAGACATTGCTCCAAATCAGAGGGTGGGAACCAAACG
Seq A exon
GTAAGTCCTCGGCCCCAGCCCTCGCCTGCCACCTTGCCTGAATGTCCCATGCATACATCATATACACACACAGGAGGAGATAGCTCCTGGTCCTCGGATGGCAAATGTTGTTCTGTCCCTCACACTGGAACACTTCCCAGCCATATCTAGCAAGCACCTGGGCCAAGAGCATAGCTCCGTACAAGTATGGCCTTGGAGGAAGGCAGTGAAGAAAGAATTTGGAGTAGAAGACCTGGCTTGGTAGCACACACCTTTAGTCCCAGCACTCAGGAGGCAGAGGTAGGCAGATCTCCGTGAGTTTAAGGCCAGCCTGGTCTACAGAGCAAGTTCCAGGACAGCCCAGTCTACATAGCAAAACTCTTGTTCAAAAAAGGAAATAGATTTTGAAGCAGGGTTGGGAAGGGTAGATCCCAGACTCTGGAGGAGGCCAGGGAAATGCTGCAGGATGGTGGGTGTGAGGAGTGAGCTCAGAGAGTGAGGCAGAGCTAATATTGGCTGGGACTGGAATACCTGGAAGGGGTGTGGCCTGGAAGGGGTGTGGCCTGCTCTCCACTTCCTTTGAGAAGAGAAGAAAATGTATAGCTGACATCATGGGATGGAGGTGGGTGTAAGAGGGGGTCTATGTGAGCTAATTATGCTGCTGTTTTTGTCCTTCTGACCTGAGATTCATCTACCCAGGCTCCAGAGTGTAGGTGGGCATCTTACATCATAGAATTACACAGGGTCACTGCTCAGTCACTAAGTGTGACTTCAATCACTTCGAGATTTATTTTCACTTGTCTGAAGTCAGCTTAAGATTACAAAAGAAATTGAGTATGAAATTTAAGCTCTCCTCATCACTGTGTCCCCCTCAGTAAAGCGAAGGTTCCAGCAGTATCCCACTGTTGCCATCTGTGTGGCCCCACCACGGCAGCCTGTGCTGAGGAATCCAGACGGGCTCCAGAAAGAGTCGTCAGCGCTGAGCTGCCGTGTAGATTTGAATCCAGAAAGGCTGTGCAGTAGGAGATAAGGCTTCTGCTCCCCAAAGAGCTGCATTGGAACAGCCGTCTCACACACCCAGACCTCAGCACCAATTCTCTGATAAAGAGAACCGTCCTCATGTTCTGCATAACTCTTTCTTCCATTCCAG
Seq C2 exon
ATACATGGCTCCTGAAGTACTTGACGAGACCATCAACATGAAGCACTTTGACTCCTTCAAGTGTGCCGATATCTACGCCCTCGGGCTTGTCTATTGGGAGATTGCTCGGAGGTGCAATTCTGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000006934:ENSRNOT00000009345:6
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:
PF0006920=Pkinase=FE(18.1=100)
A:
NA
C2:
PF0006920=Pkinase=FE(14.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
AGCCTGGAATTGCTCATCGAG
R:
CTCCAGAATTGCACCTCCGAG
Band lengths:
279-1408
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]