Special

GgaINT0144048 @ galGal4

Intron Retention

Gene
Description
mannose receptor, C type 2 [Source:HGNC Symbol;Acc:HGNC:16875]
Coordinates
chr27:2412671-2414264:+
Coord C1 exon
chr27:2412671-2413069
Coord A exon
chr27:2413070-2414090
Coord C2 exon
chr27:2414091-2414264
Length
1021 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGG
5' ss Score
9.68
3' ss Seq
GGGACCCTCTTCTCCTGCAGAGA
3' ss Score
8.7
Exon sequences
Seq C1 exon
ACTCCAAAGTCTTCCTCATCTACAACGTGGGTGCACAGGGCTGCCTGGAGACGAAGGACTCGCTGGTGCGGCTCGCCAAGGGCTGCAACGCCAGCTCCCCGGCCCAGCAGTGGAAATGGGTCTCACGCAACCGCCTCTTCAACGTGGGGGCCATGCAATGCCTGGGGGTGTCGTGGCACGGGGGCAATGCCACGGCTGGCCTGCACCCCTTGGCCACCTACGAGTGCGACCGCGAGTCTGTCAACATGCGCTGGAGCTGCCGTGGTCTCGGGGAGCAGCTCTCACAGCACCTCGGGGCCCGACCAGCCAACACCTCGCTGGATAGGGGTGACCAGGCACGCAGCTCACAGTGGAGGACATATGGAACTGAGGAGGATCTGTGCTCCGTGCCCTATTCTG
Seq A exon
GTAAGGCCCACTTGCTGGGCTCACCATCTGCGTCCCTTGGTGCTTCATAGCATCGCAGCATGGTTGGGTTGGAGGGGACACAAGGCCCCCACAGGTCTTACCCCTTGCTGTGGGTTGGTTGCCCCCCTCCAGATCGGACCCCGGAATTGGATGCAGTATTCCAAATGGGACTTCCCTTCTGTTAGTGTTCTTTGCCAATCTGAATAATTCAGTGGTTCTGTATCAGCACAGTGGTGCAGTCGCTGTCGCTGGAGTGGCACTGAGAGAACATGGTTTAGTGGGCATGGTGGGGGTGGGTTGGTGGTTGGGCTTAGAGATCTTTTCCAACCTTAATGATTCTGTGATTCTCTCTGTCCCCATTGCCTTGATGCCTTGCAGACACCCAGGAGCCATTAGCAGCAGTGTTAGCCCCTAAGCAAAAGCAGTCCCAAGCTAAACACCATGCAGTTCTTTGCCCCAACCCTGCAGTGGAATGGGGGAGAAAAGATAAAGAAAATAAGAACTTGTGGGTCGAGATAAGGGCAGCTTAGTAAGGAAGAAAAAATAGGGAAAGAAAAAGAAAAAAATCAACAGTAGCCAAAAGAATAAACAAAGCAAGCAATGCGCAAGGCAATTGCTCACGACCAGCCAGCTGATGCTCAGCCAGTTCCCACAGCCCCCACAGCCAACTCCTCCAGTTTTATCATTCCACATGACATCGTATGGTCTGGGATGTCCCTGTGGCCAGTGTGGGTCAGCTGTCCTTCTGGTTCTGTGCCCTCCCAGCTCCCCCCTGGTGGGGCAGTGTGAGGAGCTGAGTCGTCCTTGACTCAGTATAAGCACTGCTCAGCAACAAGTAAAACATTACAGTGTTATCAACACTATTCTCATCCTAAATCCAGAACACAGCTCGTAGGGAGAAAATTAACTACCCCAGCCAAAGCCAGGACATCCAGGCACCCCTTGGTCCCCCAGTCAGGAGAACCCTCATCCTCAACTCCCCCTGGCTGCAGCCTCATGGGGGGACCCTCTTCTCCTGCAG
Seq C2 exon
AGATCTACACCATCCAGGGCAACTCACACGGGAAGCCCTGCACCATCCCCTTCAAGTATGACAACCAATGGTTCCACGAGTGCACGAGCACAGGGCGGGAGGACGGCCATCTCTGGTGTGCCACCACGCAGGACTACGGCAAGGATGAGCGATGGGGCTTCTGTCCCATAAAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000461:ENSGALT00000000627:1
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion (1st CDS intron)

No structure available
Features
Disorder rate (Iupred):
  C1=0.145 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0004014=fn2=WD(100=71.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGAAATGGGTCTCACGCAAC
R:
TACTTGAAGGGGATGGTGCAG
Band lengths:
347-1368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]