Busch Lab

ZMP

dis3

Ensembl ID:
ENSDARG00000060559
ZFIN ID:
ZDB-GENE-080213-3
Human Orthologue:
DIS3
Human Description:
DIS3 mitotic control homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20604]
Mouse Orthologue:
Dis3
Mouse Description:
DIS3 mitotic control homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1919912]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa25602 Nonsense Mutation detected in F1 DNA Not yet available
sa24850 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25602
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085454 Nonsense 24 950 1 21
Genomic Location (Zv9):
Chromosome 1 (position 29818390)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 29958202
GRCz11 1 30762133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAAAAGACCCGTTCTGGCGGAGTGTTGAAAATCGTACGGGAACATTA[T/A]CTCCGAGATGACATCTGGTGTGGAAGTGAAGTTTGTAAGGAGTGCAAAGA
Long Flanking Sequence:
AATCGTTTGACTTTGGCTAGTAGACTAAATCTTTACTGTAATTAAATATTTTCAGGTTACTAGAGCTAAAATGTCGTCAAAGATGTCGAAATTTTCGTGAATCGTAGGAATTTTCCGCCATCTAGTGTTGAATAGAGTGAAAATGACAGAAGATTAACATGCTCTAACTGCTTACAGCCTCCCAATAATTTACAGCATTTTCAAACACATTGTAAGCCATTTTATCGGCGCATGTGTGAGTTCAGCCAAATATTATAGAATACACTTAAAGTGACTTTGGTTCTTCGTTGTAAGTAAGACTAGGAACCTTTATGTCGCTGAATCACCCCGGAACAATATAGAGGCGGCGCGCGGCTGCACACGCGGGTTCACTGTGTGCTGTGTTTTGGTGGAACAGCTCTTCAAAACCGCTTGACCATTAGCTTGACCATGTTGAAGTCCAAAACATTTGTAAAAAAGACCCGTTCTGGCGGAGTGTTGAAAATCGTACGGGAACATTA[T/A]CTCCGAGATGACATCTGGTGTGGAAGTGAAGTTTGTAAGGAGTGCAAAGATGAAGCTCCGGTGCTGCAAGAAGAAACTTGTATAGAAAGCAACCTCTGCCCATATCCTCACTATTTAATCCCAGACACCAATGTGGTTTTACATCAGGTACATTCTGTTTTTTTGTTTTTGTTTTTGTTTTGTTGTTTTATATGTGTAATTCACTTGTCTGTAGTTGAACCCCAACATTGTATTCAGAATATCAATAAGATATTCAATAAGATATTGAATTAACGCTAGTCCGTTAACGTTAGACTTTTTGTGTTGTCAGTGTATGACAAATTATCATGAGGAACCTTATGAAGCGGGGTTAAAAAATCTGTAACGTTAGTTGGCTTAAGGGCTTTAACGTGTACTTAAAAAAATATGACTGTTTTTTGTTATTTGTATTGTGTTTTGTTGTTTATATAGGTTAATTAATTACGTTTTATTTATTTAACTTTAGTTATTAAAATAGGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24850
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085454 Nonsense 379 950 8 21
Genomic Location (Zv9):
Chromosome 1 (position 29809299)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 29949111
GRCz11 1 30753042
KASP Assay ID:
554-7530.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACCAGGCAACAAGACACCTTTTCACTCCAGCAGACCGGAGAATCCCA[C/T]GAATCCGCATTGAAACCAGACAAGCTGCCACACTGATTGGACAGAGGATT
Long Flanking Sequence:
AACTGGTGAAGTGAGCCATTTAAAGATATAATCTTGCGTCTCACAATCTTTGCATCTCACAATCTTGTTTAAGAAAAATTGCAGCCCCTTCGATCTTATAAAAACATGTTTGGAGTAAGGTGATAATTTTTTTTGGATGGACATTGTATACAGTTGTCAACATTTGAAGTGAATGTTAACCTTTGAATAAAGTTCTCCTAAAACAATTAAACAACATTAAAATTGTCATAAGACAAGAATGGATTGACTTTTTTGATCCACTTCAAATTTTGACCCTGTGTATTTTCTAAAATAAGATGAAAGCATGCAAACATAATTCAGTTGTAGCTAAAATAATGTCTAGATTTTGTAGCTTGGCACAATCTTAAAAGGCAAAATGACCAAAAATGTATAAAATATTATATTCCTTTCTGGTGCATTTACTTTATTTTTTGTATTATTTTGAATTTAAACACCAGGCAACAAGACACCTTTTCACTCCAGCAGACCGGAGAATCCCA[C/T]GAATCCGCATTGAAACCAGACAAGCTGCCACACTGATTGGACAGAGGATTATGGTTGCTATAGATGGATGGCCTAAAAACTCAAGATACCCAAACGTAAGTGTTGATTATTTTTGACATCCTTTTTTTTGCAATATTTTAAAGGGCACATAGTTTACCCCTTTTTTATGATTTAATATTAATATTATAGTTATTCTGAGTGTGCCAGTTTAGCATCAGTTAAAAACACAGTTCAGATTTTTTTATTATCATGTGTTTAAAAGTGTCATGCGTGTGGACAGCTCCCTGTTTTAGAGGCGTGTTGCTTCACATAAAAATTAATTTAAAATTCCCGGCCAATGTAACAAGGGGGCAAAGCTAATAGCTCCCCCGCTCTGTGTTTGGCAACAAACAGGCAGACAGAGAGAAGCAGCATGACAGGATCAGCATTCAGCCGTACATGTATGCCTCGGACACGGACCAAGCAGAGAGTGCACAATCATTTGTGTCTTTGTATAGTTT
Associated Phenotype:
Not determined