Special

GgaINT0034839 @ galGal4

Intron Retention

Gene
Description
crumbs family member 1, photoreceptor morphogenesis associated [Source:HGNC Symbol;Acc:HGNC:2343]
Coordinates
chr8:2494710-2497968:-
Coord C1 exon
chr8:2497840-2497968
Coord A exon
chr8:2494837-2497839
Coord C2 exon
chr8:2494710-2494836
Length
3003 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGA
5' ss Score
8.94
3' ss Seq
TTTTGCACTCTTCCCTGTAGGTG
3' ss Score
11.82
Exon sequences
Seq C1 exon
ATATCGAAGATTACCCTATACAGTTTGTGGGAATGAAGACAGAAATCTCACCTGTTACAATTACGGCAACTGTACTGACCTTGGAGGCAAGCTGGCCTGTGTGTGCCTGCCAGGATTTGCTGGAGAACG
Seq A exon
GTGAGATGCTTCACTGTATGAAAAAGTTCTTCCAAAAGTCATTCCAAAGGTTCTAGGGTGTGCCATCTATAGGGAAATTACCCTCCTGCAGAAATACAGAAAAAACTGGTTTTCAAGCAGAGCAGTTCTTTGCCCGAGTGCCTTTCAGAGCCTGAAAGTATAACAGTCTTACTCAGGCAAAAAATACAAATTAACTCAGCAAGGGTCAGTCCAGTACAGCACCACTAATGCCAGTACAAGCCTTTATTTCTTAGTCAATTTTGTACACCTCCTACTCTTTGGATTCAATGCCAATCTAGTATATAGGCAAACTGGAATGTTACCTTTCTATATATAAGCACATATAAACACACATATCCTATTCATATATGTATAAAAATCAGCCAGCATACAATGACACATAATATGCCAAGCTGTTCTATTTTCACATGTATCCATTGTGAATATACAAACTATTCCCCTACAGGGATAATGACATGAAATATGTGGTGGTGTTATTTTCTTTACTGAATGCCAAAATATGAAAACAGAATTATTATTTAAAATCAAAGTTGAGAAATACTTCTTACATATTATAGTATAAAAAGGAAGGGGCCATCAGCCTTCCCAGTTTGTACCTTGTAGCAGGTCACTGCACGATCACTTACCACTTGATTCTCTACAAACACCTCCACAGCAGGGAGGTCTTCAGGTCTCAGTGCATCAGGTGTTGTAAAAACATAAGAGGACACCATCCCAGTCATAATACGGCCTGAAGTAACGGTAAATTTCTGAATAGTAAGAAAAGGCACACAGAACATAAACAGAAAACTAATGACTTTTGCTTGCAGTGCAATTTAACACTACCTCAGAGTGCAATATCCAAACATTCGGTAGGACCAAGTTGTGCTGGCTTTGCAAACATAAAGCAGTTTTCAACAAATGGTTTTCATTCTTTCAAAATCCGATTAATTCACTGACTTTGTGGAACCTGTACAGTAAACCATAAAGGACAGATGAAATGAAAATTTCCACCCACTCATTGAGCAGTGTAGTTGGCTGACGCATCTGCACCGTACTCTTTAACTCAGCCAGAAGGCCTGCCTGCCACACCACAGAAAAAAGATTAAGAAATAAAATAATAAAAAAATAAAAGCATATTCTCAGGCAGTTCTTCAGTGTGTATTTTTTTTCAGGACTTCAAGATAAGGCAAAGTGCTTTTTCCTTCTTCCTTCCCCTGTCAGGCAACTCGCTAAGTGCAGCTCTGGGAATGAGCCTTGCTTACATCCACCCCACTGGCTGGCAATAATGTCTATTTTATGGTTCCCGTGATCCTCATATTGAGCAGCAGCCTTGCACCAAGCATACTGCACTGTAACTGACTATCAAAGCAAGGCATTCTTCTCAAATGTCTAAAATTGACTATTTGTCCTCTTTTCCTCCAGGCTGACACACTGTAAACCAGAAATATTTCTGTTTGCAGAACTTAATACATCAGAAAAGAAAATTTCACCTCAAACGTTTGACATTTATTTTTTTAGAACAATTTCAAATGTATCAGTTAACAAGAAAATTCAAAACAAAACCCTTCAGTCTATTTATTGATTAGAAAAGTAAAGCAGGCATTTTGGCTTCAAGACAGTATTTCATCCCTAAGAAAAATAATGATATACAACATTAAAAAAAAGGGGGGTGGGGATGTCTTTCTATGTCAATCAATTGACTCGAGATTACAAGGAAAAAAAGAAATAGGAAATAATAGGTGGAAAGAAAAACTTGAAAAGATTAAAAAAAAGGAGATGTAGTTGTCTCTTGAAAACAGTTATTTCACTGAATTCAGGCAGTTTTCAAAATCACCATGGGGAGTTAGGTTTAAAAGTCTTCCTGATGTTCAGGAGGACTCAGGTAACAAATTCCCTGCACTATTTTGTTTTCCAGTTTTGCATAGGGAAGTTCATAGCTATATAATTTTCACGGATTGAATTAATACTTAATTTTCAGCTTTCTGAAGTATGTAAATATAATTGATCATTGAAGCAAATGACTGAAATTTTTTAATGGATTAATAAAGAAAACCATCTAAGAGTGTTTAAGGCAAAGAACAGCACATCTCCAATGTAAAACTAACAATGTCTTGAGTGGTTATGGATATGATTAAACAAAACAATTCCTGGTAATTTTGAGTGAATTTAACACATTCAACTTCAGTGGTAACTGTGATTCTTTATGGGGAAAAAAATAGTATTGACCATTATCAGTATTTGAAAGAATGAAGGCAGGGAATTCAGGGGAAGCTTTGTCAGGACAGAGAATCACCAAATCATTACCAGTTTTTAAACAGTTGCAAATGCTTTTCATTAATGTTCAGTTGGTTGCCTTGAGAAATTATTAGAGCTCAAATTTCCCTTCTCATCAGAATTACTGAAAAGCATATAATGATACTAATTTAAGCTTTTAAAACCTTATTCTGCAACTGTCTTTCTTAACATTCTTAGTGCCCACACCCTCTCAGAGAGACCACATAGGAGGCTGTGCTGGACATCTACTGACATTTCAAATTGAGAAAAGAAATGGGTGAACATTCCCAGGGGCATTCAGTTGTGAAAAAATATGCTTTTGTTTAACTTAAATCTAAATTATCATGAAGGAAATTGGGCCCTCAGCTTGCAGTAATGATGAAAACGGACTAGCAAGTGTTCAGCAGGACTTGCGCTGTATCCAACTCTAAAACCACACGCCAGGTTTCATTTCACTTTGCTAAGCACCATTCACCAGGAAATGTGCCACAGAAATGAAATTTCTGGCTTAACTGTCTATGTTTGAAAGTAACACGGGAAGTTCAAGATTTAAAAGAGGCTAATCAAGTAGTTAATAAGATTCTCTGAAGACCACAAACACGTGGAAATATACTACAGATTTCAAATGGAGCAGCCTCATTAAAAGTTACTGAAATAAAAATGTGCCGGTTTTATTCATTTTATACCTGATGTCAGGATTTCACTTTTTTGCACTCTTCCCTGTAG
Seq C2 exon
GTGTGAAAAGGACATTGATGAGTGCAGCTCTGATCCATGCCTGAATGGAGGCCTCTGCCAGAACCTGCTCAACAAATTCCACTGCCTCTGCGACGTCAACTATGCTGGAGACCGCTGTGAGATCGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002287:ENSGALT00000003596:9
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:
PF0000822=EGF=WD(100=72.7)
A:
NA
C2:
PF0000822=EGF=PD(0.1=0.0),PF0000822=EGF=WD(100=72.1)


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:
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]