Special

GgaINT0034837 @ galGal4

Intron Retention

Gene
Description
crumbs family member 1, photoreceptor morphogenesis associated [Source:HGNC Symbol;Acc:HGNC:2343]
Coordinates
chr8:2498516-2501880:-
Coord C1 exon
chr8:2501715-2501880
Coord A exon
chr8:2499420-2501714
Coord C2 exon
chr8:2498516-2499419
Length
2295 bp
Sequences
Splice sites
5' ss Seq
AATGTAGGT
5' ss Score
5.12
3' ss Seq
CAATTATTATCTTTGCACAGGTC
3' ss Score
7.45
Exon sequences
Seq C1 exon
TCCAGTCCTTGCCACAACGGTGGTGTATGCTATTCAATCTGGGATGACTTCACTTGCACTTGCCCCCCTAACACAGCAGGGAAAGCTTGTGAGGAAGTTAAGTGGTGTGAGCTTGGGCCCTGTCCTCATGAAGCACAATGCAAGCTGGCGCACCAAGGATTTGAAT
Seq A exon
GTAGGTAAATTTCAGTTATTCCTGTCATCTTTGGAAATTAGAAACAATTGAAATTTTCATCAATATTTCCTTAAAACCAAATATTTACTTATTTGAAAATTCAATGCTATTTCTATATTATGTAGGTTGCTCTGAATGTAATGCCTCCTATTTTATTATCACGGAAATGACAACAGTTAAAGGGAAGGCAGTAACAGTATTTAAGGGAGCAAATTCTCACCTACAAAGCACCGTTCTTCAACACAGTCACCACCAGTAGCTGTGCATTTTCATCAGTGATGAACAAGAGCCTGCATGCTGCGTTTGTGAAAATCTGCACCAGTGGAGGTGACCTGCTGTCGCTGTCACCGCTGCTGAAATGCACCACCCCATCACTGCACTCTCATCCACTGTTTGGTCTCCATAAATGTTCAGCAAGCATCAGTGAATGTCATATTTTCCCTGCACAGAGGAATTCAGGGATACACCTTTGCTTCCTAAACACTTTCATATCAGATGCCAATGTGTCAGACTTCCTCTCTGCTTCTGTCTGTTGCACAGCAAAAAAATGTAATGGGATATTGGCAGGAGGGCTCAACCTCTACTGTCATACCACCACCATCTGCCTCTGACATCACTGGCCAATGTAATAAAATAAGAGGCATTACTTTCGGAGCAGCCCCATATAATAGCAGAAATATCAATAATAATATCAATTGTAAGTTATATTAATGAGAATATCCTGCCATATCGACCTCAGAAATTTTCAACTAGACCCAACAATGCAGGCACTGATGTTTACATAACCTTTGCTTTTGTCTTATCCAAGAGAGCATGTCAGAGTTGTAGAATAGATCGCAACATTGCCAGACTGCAAGTGTACCCCACACCCCTCCACTGCAAAGAGATAGGAAGACATCCAATGTTGGAGCAACCTTAGGATGTTCTCCATCCTCCTGAAGATACAAGTTACATGACATAAATTGCATCACTTGATTTTCTTCAATGTTAATTATCTTTGTAGAAAGTCACCTTAACTCCAGCCATACAGTTATTAAATTAGTATCTTGGCAAGAAGCACTTGCATGCCAAGTGGTCTATTTGTTTGAAAATTGATAGCCACTGGCTGACTGAACATAAGCCACCCTGCACATCTTTCCTTCTCTTTCTTTCTCCTTACCACCCTGAACTGGAGCAGAATATAAGAAGAAAGTAAGAATTTTGAAGCAATATTTTCTGGTTTTGCTAACAAACAAAATTTCTAACTATGCTATGAAGGAAGAGAAATATATACAGAGTCTGTTAGAGTGGCTGATTCTTAGGAATGAGAAGGTTCATCAACAGAAGATTTCTATCATGGGCAGTTTGCATGCAGATCAATATGATGCTGTTTTCATTGAGATTGTTAAAATCAGCACTGCAGCACATGTAAATATTTACAGCTGAAGTTAAAATAATTGCACCGTCTCTAATGCACATGTTTAAAGATGGCATCAAATATGCTTTCTCAAAATTCACTTTTACATTTTAGGAAAACTTGAACTCCAACTATACAAAAAAAAAAAAGATAGAAAAAAAAATCAAAGCAACAAACCAAAACCTAATCATAAAAAACACCCACAACAAAAACACACACACACACAAATTACACAAGAAGAAACACAGACAGAGAGAAAGCTTCGAAAAGAAGCTGATGCAGGAAGAGTCAAATAACAACAAAAACTTATACTCAGTGGCACAGATGACAGTAAAAACCTCTTCCCAAATACTATGTAGAAAACATCAGTGCAGTTACGTAAGTCAAATTTGGCTACACCTGTAAGCCTATACAAAGCTACTGAGCCCCATCAGCACCTCAGGCAAACCAGTGCAGACCCACTGGCTATGGTAGCCTGGTCCTTAACTATTATTTCTTTGCTAAGTGCTTATTCTGGGCTACCCTCATGAGAAGAAGCAAGGCTCAACTATTATCTACACTTGCTTGTTTAGATTAGCTTACTGGTTTTAGTAGACCTACTTCTGATTTACATTACAGTAAATAAGGCCAGAGTCATCGGATCAGGGTCACTGTCCCCCTTTCCTCGTTAAAGGGAAATGAGCTGGAAGCTTTAGGATTAGAGTTTCAGGTAGCACCGCCCTGTAATCTTTGCAGCCATAAGAGGCAAGCAAGGATAACTGGGACACTGATGGAACTGGATTGCTTTTCAGTAGAAACAAAAGGACTTAAGTGATGGGGATCATGGGGCACTGAAGAGATACTGTCCAGGTGGACTGGTTTAAAGCTGGCCTGGTTTCTCAATTATTATCTTTGCACAG
Seq C2 exon
GTCTCGCTAATGCAGTGTTTAGCGGCCGAAGCAGTGCTATATTTTACAGAAGCAACGGGAATATCGGCAGAGGCCTCACCAATATCGTGTTTGGCTTTCGAACTAGGGACAAAAATGTGATACTGCTGTATGCGGAGAAGGAGCCTGAGTTTGTTATCATCAGCATTCACAACTCCAAACTGGTCTTCCAACTGCAAAGCGGCAACAACTTTTACATGTTGACCCTCACTAGCTCGCTGACCGTGAGTGATGGGAAGTGGCACCAAGTTACGGTCTCCATGGTGGAGCCCCTGTCTCAGTTCTCGAGGTGGCACATGAATATCGATAACAAGGACGCTGCAACCAGCACAACTGCTACCGGAAGCCTCAACTTTCTACGAGAAGAAACAGACATCCATTTGGCTGACAAGGCTTTTGACAATTTGGATGGCCTGAGAGGATGCATGAGCACCATAGAAATCAGTGGCATTTATCTCTCCTACTTTGAAAATGCTGACATCCTGACTAAAAAACCTCAAGAGGAACAATTTCTCAAAATATCTGCAAACCCTGTTCTTACGGGCTGCTTACAGGAGGATGCCTGCAGCTCAGAGCCCTGTATGCACGAGGGGACATGTGAAGACTTGTACACCTCCTATCGCTGCACGTGTCGCCCGGGGTGGGTGGGTACCCACTGTGAGACCAACATCGATGAGTGCTTCTCCAACCCCTGCATTCATGGAAACTGCACAGATGGGATCAACTCTTATGAGTGCATTTGTGAACCTGGCTACACAGGGTTAAACTGTGAAGAGGATATAGACTACTGCCAGGGCCACCAGTGTGCAAACGGAGCCACCTGCATAGATGGGATTAATGGATATTCATGCCTGTGTGCTGGTAACTTTACAGGAAAGCTTTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002287:ENSGALT00000003596:7
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=PD(90.3=50.0)
A:
NA
C2:
PF0221019=Laminin_G_2=WD(100=41.4),PF0000822=EGF=WD(100=10.3),PF0000822=EGF=WD(100=9.9),PF0000822=EGF=WD(100=10.9)


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]