Special

BtaINT0041947 @ bosTau6

Intron Retention

Gene
Description
collagen, type V, alpha 1 [Source:HGNC Symbol;Acc:HGNC:2209]
Coordinates
chr11:106935978-106939388:-
Coord C1 exon
chr11:106939332-106939388
Coord A exon
chr11:106936020-106939331
Coord C2 exon
chr11:106935978-106936019
Length
3312 bp
Sequences
Splice sites
5' ss Seq
CCGGTAAGA
5' ss Score
10.1
3' ss Seq
ACTCTCTCTGTCTTTTCCAGGGG
3' ss Score
12.68
Exon sequences
Seq C1 exon
ATGGGAGGGCCTCGGGGCGAGAAAGGTCAAAAAGGAGAACCCGCCATCATCGAACCG
Seq A exon
GTAAGACACTTTCTTATTCTCTCTCTGGAACCGGCAGGGTCAGGGGTCAGGGGTTGCATCCTGGGGGCTTGTGGCGGGTTAGGTAGGATGGGGACCCTACTCTGCTCCCACGGGACCCCTGAACCTCTGTGCCCCGGGCCACCGTGAGGAACCACTTGACCTCGCGGATGCCGCGTGCTGCTTTGAAAAATCTCTGGGCAGGAGAAGGGTCTGGACCTCGACTGGAGAGGGGTGTCTGCCGAGGTTCAAATGCGTCAGGACCCTTGGTGCCGCACGCCCAGGATCCAGGCGCATCTGTGCCTCCAGTCCCACTCGGGAAGGAGACTCGGCTCTGGGAGGGAGGGAGCCCCGCCCCCCCCCCCCCCCCAGGGAGGGCAGAGGGCGTTAGCAGGCCGCGTGGGGACCTGGAGCTGCAGGTCCCGGCCGGGGAGGACCTGTTCTCCCTGCAGCTGGTGAAACAGGTGAGCTTGGTTTTCAGCCCCCTCTAGGGGATTTAATAAAACAGCTCCACACCCAAACTCCCATTGAATAAAACTGCTCTGTGCTCGGCGACAGGGCTGGGGGCAAGTTGAACAAAATGACCGTTGATGATGCCTTGACCTTGGGAATAAGCTCAGCATGCCCCTCGTGGGTTTGTGGGTGTTCGCAGGGTCCCACATCCTCTGCCCTCAGGGAGCCGTACCTGGTTGGGAGCACCAGGGCCCAGCCCGTGGCCTGAGGCCCCGGCCCTGACCCAGGGCGGGCAAGGAGCCATGTGATCAGCCGGAGGAGGAGGGCTGCCCTGCAGCCGCATGTGGGGGGCACGGCCTTGGGGGCCGGGAGGATGCTCTGGACGTGGGATCAGGGAGGTCCTGGCTGCCAGGGTCCAGTCCTGACATGCCCCCCAAAAGCAGGAGGGTCACCAGCCTGGGGCCCGGGGCTCGGGCTTCCTCTGCCGCCAGCACCCAGGTCCTGGTGGCTGATCCCAGGGCGTGACTCAAGTGGAGGCTCCAGGGCCCCCCTGATCCCGGGACCCCTGGCATGAGACCTGAGGCGGCGCCCGTCCTTCTGTGGAACTGGGAAGGCTCTTTTGGAGCGTCACCCCCTCAGAGGCACCGGGAGCCAGGGGCCAGGGCGTCAGGACAGGGGACTGGGTGACGGTCGTGCTCTGCGCTTTCCCCACCCCTGGCCTGTCCCAGCTCCTGTGGGGCTGCAGCCACTGGGCACACACAGCCTGTTCTCAGGCTCAGGACACCCCCTTTCCAGTGCTCCCCGAGGATCCAAGGGAGACAGGGCTTGTCTGGGGTGAGGGATGGGGGTGCAGGGGAAGGGGGCAGGGTGCCAGGGTAGGGGCCCAAGGCCAGGTCGCCCCTTGCTCAGCGACATGAAGCATCCTGACACCAGGATGTCCGACTCTGGGAGGGCCTGCCTGGCATCTCGGTCCGGACGAGCATCCTGTTCGCCCATCCCCCAGCCTGGGCTGCCCCTGTTCGAGGGCCGTAGCGTCCAGATCTGGATGGAGGCTGGTGAGGGGGGCGCGGGGTGTCCAGGCTCCACTGCAGAGGGCGGGTGGAGATGCAGGCTGAGAACAGAGAAGCAGTCCAACACAGCATGTCTGCAGGACGTCTGGTCCAGCCTCTTCCAGGGGGCCATCTGATGCGCTCTGGCCCCATCATTCCCTCCAGCCCAGCCCCTAGCCTGTTCAGAGTACCCGTGGGGTGAGGCCAGTCCCTCTGGGGACACCATGTAAGCAGTTGGAACATCTCAACCTGGAGCATCGCTGGCTGTCCTCAAGTCTTAGCTTCCCATAAACAGAGGGCCGAGCCCTGGGAGACGGCGGAGGTGGTCTTGACACATCCTGGCCTGTGGAGGTCAGGGGGCTGCTTGCTGTCCCCGACCTGCCCCAGTGACCTCCCTCCAGGGCGTGTGACTTGCTGTCCACGGAGATTCCCTGTCTCCCTTGGAATCAGCTCCTCTCTCTCCATCCATCCATCTCAAGGATGTTTCCCGCCAGAGCTGTTTCCCACTGAGATCCGGTACCGGCTGTCATGGGTCAGCATCGCCAGTGGCTCGTTGAAAGGACAGGACCTCCCCCCAGGGTGGGGGGGACTCAGGTCAATGAGACCTGGTGCTCCAGGCTGCGCTGGGCCCTCAGGGACCTGGCGTCTCCCCATCCAGGAGCCCGAGTCACCTGGTGAAGGCCCATCGCAGGCGTGTCCAGCCTCCTCCGTGGTTTAAGGAAGGTTTTCTGGGCCCTGCTGCTTAGCAGATGGACAGCCCGCCCTGAAGAGTTGTGTGGAGCTCGGCTAAGGCTGAGACCCCCTCCTGGCGGATGTGGACTGGGGCCTGTGCAGGAAGACCCCCTCTTTGTGCCTCGGGAGCGCTCCTCGGTGGGGTGGTGGCCGCGGGTCCCTCCCCACTCCTGGGAAAGTACAGGTGCCCCTCCGCCGGGCCCACCCATCCCGCAGCCCCCAGCCCTCCCCAGGCCCGCGACCCTCCTGTGAGGGCCCGACCCCGGGCCGGCTCCCTGAGAACAGAGGCGGTGTGTCCGCGGTGTGGCAGCCAGGGCTGTCTCCCTCAGTCCCAGCTCAGTTCTGAGCCTGCTTCGCTGCCGTGGTCAGAGGAGCCAGGGAAGCCGAGAGTGAGGAGGCGGCCGGAGGAGCTCTGTGCGCGCCTCTGCGCACACAGCTCTGCGCGCACAGCTCTGTGCGCACATCTGTGTAAACACAGGGTGTGTCCTCCCGGTGTCCGGGGGCCCCGGGGGGAGGACGAGGGGCTTGGTCTGCAGGGGCCTGGTGTCCGACAGCGAGGCTGGGGGCTGGAGGCTGCGTGGACCTGGGCTCGGCCGGGGGCGGGGCTGGAGGGGGGTGGGGTGGGGCCGAGCGCGGCCTGTCTGAGCTGTCGGCCCCAAGGGGCCTCGGCCTGTGACCCCCTTCCACTTGTCCCCCTTGAACCCCCAGGCTGCCGTCTCACCTTCACTGGGCCCTCGGCCTGGGGTCACTGCCCCCTGGGCTGCCATCACCGAGGCCTACCTGGGCACTGCCCCCTGGGACAGGAGGCCAGCAATGGGGCCAGGGGCTGGCCCCCTCTCTGTCCTCTGGCTGGAGGTGCTCAGAGCTTGGTCACTGCGGCCCCCACCACAGCCCCACGGCAGAGGCTGCTGCTTCAGACCCGTGCCCAGGCAGGGGGTGTGGACCCAGAGGCCTGGTCCTTGGTCCTGTGGGCCACCCGGCCTGGAAGCTGTCCTTGGGGCTGGGGCTGGGGGGCCAGGTCCACGTTTCGGGATGGGGGAGGCCATCCTAGGGGCTCAGACACTCTCTCTGTCTTTTCCAG
Seq C2 exon
GGGATGCTCCTGGAGGGGCCGCCTGGCCCCGAAGGCCCCGCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000047998:ENSBTAT00000063052:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0139113=Collagen=PU(18.9=71.4)


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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development