Special

GgaINT1017718 @ galGal4

Intron Retention

Gene
Description
multiple EGF-like-domains 10 [Source:HGNC Symbol;Acc:HGNC:29634]
Coordinates
chrZ:56241215-56244644:+
Coord C1 exon
chrZ:56241215-56241378
Coord A exon
chrZ:56241379-56244541
Coord C2 exon
chrZ:56244542-56244644
Length
3163 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGTT
5' ss Score
6.3
3' ss Seq
TTTTGTTTTCCTGGCCACAGGAC
3' ss Score
9.7
Exon sequences
Seq C1 exon
GTTGGCATGGTGTAGACTGTTCAATCAATTGTCCCAGCGGTACCTGGGGACTTGGCTGCAACTTAACTTGCCAGTGTCTTAACGGAGGGGCTTGCAATGCTCTAGATGGAACCTGTACCTGCGCTCCGGGCTGGAGAGGAGAGAAGTGTGAACTCCCTTGCCAG
Seq A exon
GTAGTTCAATCATTTTGATGAGTATGGCACTGTATTGATACTGGGCAAGGGGACACTACTGTAATTCTTATCACTTCATGGGAATAAATCCCCAACAAGCACTGCACCTAACAGTCATCCCGTGTTTGACTAGATTCAAGATTAGGGACATACACCAAAAAATCTTCTGGAAGAACTCTGCTGCACGGCACACTGAAGCACAGAGTAGGATGACTAGCATGATTAAAGTTGGTAAAGACCTCTAAGATCATCAAGTCCGGCAGTGATGACTGTCCAAGAAATGACTACACAAGACAAAGATGAACAGATGAACATTTTTTTTTTTTGCTTTCACACCTGAAAGTTTAACCTGAGACTTTTTCCATGCTCCTCTAGGATTTATTGAAAAACACAGTACCAACTTTTCTCTCTTTTTCAGCATAAAATGCCATCCAAACTGCTTCTATCAAACTACTTTAAGGAAAAACAATGACAGAGAAATGTAGCAAAGATATATTCCACATTTAGCAACATAATTTTAATTAAATTAGCCATATATGTGGTAAGGTATGAATGAAGAACTTCCTTTCTCAGTCAGGCAAGAGAAGGCATTCTTATCATGCAATCCCATGGCAGACTTTTGCCTTTATATTGGACTGTGGCTTCTATTATACCCCCAGACAGAAATCATTCTGTAGACAGACACGTGTATAATCAGTTCTGTTCTACACTGTAAGAACCCATAAAAATCCTTAATTTCAAAGCACAGAAAGATGGAAAATGCAAACAATTCGTTTTACTATTCAACTATTCTAACTACATTTCATAAACAAAGCAAAAATGATTTTTTGGTGAAAAAATGTATTTTTCCAGAGCCCATCTTTTCTAATGACAGATTTCAGTTTTCTTGGACATTTTAAACAACTATTAAACAACTATTATTATTATTATCAAGAAACCTCTCTCTGCTCTTCTTTTCCTGTCTTTGTCCTCCTTTCATTTCTGCAGTGTCATCTCCCTAGCAGGTTGGTGGCATAATGTAAAAGTAAAGGAATCACCTGAATTCAGTATGAACCATCTAAATTCCCTGCGCACATCATATTCAAGCTTCTGTCGGTTTGGATTACCTCTGTTTAGCAGTAACACAATAAAAGTAGCTGAACTACAGCATATGAGTGGAAGCCACACCTTTGTTTTGAACGAACTGCTCTCAGAGTGTTCTGAAAGAATTTTTTGGGAATGTTTTTTGGTTTGTTTTTAGAGGTAGCTTAGCATATGTTCGTTCTGATATAGTAAATAAAGTGACACACAAATTCTAAAATATTCTGGAAATCTGATTAGAGTGCTTCCTGTGTGTGTTTATGCAGCATTTCCAACAAATGCATCTCAATTAGAAGACTAATTTTTGTTTTTCTAAAGAAACTTTGCTTATCACTTAGTGTCTAATTCTGAAAGATGTTGGTAAGTATCTCCTAAGTTCCATTAGCTCTTCTAAAAGTGACTCCTTAAAAAAATACCAGTAGTTTCATCCCACTTACTCCACTGTTTCAAATATAGCAAGCAAGTGCTCAAAGGAAATTCCCAAGTTTACAATTCCCAACCAACTTACTGTCATGTACTCTCTCACTCTCCACCCACCTCCTTTTATTTCTGTGTCAAATACTGTCCAGAATCATTTCCATATGCAAATACATATCAGTGAATTTCATTTTTTTTTCATTAGATTTAGAAAATCAATACCACTGTTCAGATTGTTAATTAAGATTGACTTAAGTTTGGACAAAATACATAGCAGACTAGAATACCCTTTTTCAGCAATATAGTTCAGAATTTCCTTTATTTCCAAATCTGATAACATACAAAGGAAGTGCCTTCCTTAATCTTTTCTTTTTCTCTCTATAAAAATGGATTCTTGAGATAAGCAAAACACTCCTTATTCTCAAGTAATGCATGATTTTTTCTACTTCAGACTTGAAAGACTGGGAATGGAATATCTGTGTCCTGTGAAACTCTACAGAAAAAAAAAGAAAAAAAAAAAAAAGGAATACCAGATGAATTTTGATACGTTTTATTCCAGTTTTTAATGTAATTTGACCAATTTTTAACCTTGAATGTAAATGTCTGTCTTTCAAATCTGACATATCTTTTCTTTAGTTATTTCCTCTGGTGTGAATAGCCCCAGAAGTATTAAACTAAATTATCTTTCTGTTTTCCTTGGTTTTGATACTTTCTCTACGTTATCTATATGCTGATGTAGTTTTGCCTTCTTTTGAGAAAGCAATTGTAAAAATTTTATTCTTTTTCTTTTTTCTCAGATTGACCTTATATGAAATTATTGTCTAAAAGTATGTGCCACCTTCTACTGAAGAAACAGGAAGTAAAATTGATATATTCTGATATAATTCTATGAAAATCAGCTGTGTTCTTTTGGCACAGTTGAACATACTGAGAAGGTTATTTAACTTGTAATGTTAACCTTTTGATAACCTTATTTGTTGGTTCAAAAATGTTCAACAGCCAAAATATAATTTTGTGTAATGTGTAATAGCCCGAGAGCTTCTTTTCTAATATATTCTATGCTGATATGCAGAGGAAAACATTATGAAACAAAAGAAAGTGATACAGCATGCGTTATTTATGAAGTAAACTTTACACTAAACATGTATTTTAATACAATGGTTCACTCCTATTCAATTCTTTTTTTAGAAATTCTGGGTTTAAATGGCACCTTTTTTCATTTTCTTCTTCTTCTTTTTTTTTTTTTTTTTTTGACAAATACATGAAAATAAGATCTGAGGCAGGAAGGAAAGTGAATTAAATAATTAAATTAATATCACATCTCCAGGAATCCTGGGTTCTAGACAGGGGACTCAGCTGTAAGAGACATTAGTGGGACAAGTACAAGAAACTTTCATTGCTACCACTGATAGGTAGACTTCTGTTTTCTGAATATTTATCCAGATAGTTTAATTAATTCTTTATCTCCCCTACTCAAATAAAAGAATTAAAATGTAGAACATCAACATTTTCCAGAAGCCAGAAGCATTTTATATTAAGTAAGCTGATTACAGGCTTAGAAGAGATCTGAGGTTTCCTTTTTTCTGAGGCAGGACTGACCAGAACTTGTTCTCGTCTAACTCTCAGTTCTCATCATCTCTGTTTTGTTTTGTTTTCCTGGCCACAG
Seq C2 exon
GACGGTACATATGGCATGGATTGTGCTGAGCGCTGTGACTGCAGCCATGCAGATGGTTGTCATCCTACCACGGGTTACTGTCGCTGTCTACCAGGATGGTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000014699:ENSGALT00000023694:12
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:
PF126612=hEGF=PU(69.2=25.7)


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]