Busch Lab

ZMP

cdc25d

Ensembl ID:
ENSDARG00000075599
ZFIN ID:
ZDB-GENE-090313-74
Description:
cell division cycle 25 homolog d [Source:RefSeq peptide;Acc:NP_001128154]
Human Orthologues:
CDC25A, CDC25B, CDC25C
Human Descriptions:
cell division cycle 25 homolog A (S. pombe) [Source:HGNC Symbol;Acc:1725]
cell division cycle 25 homolog B (S. pombe) [Source:HGNC Symbol;Acc:1726]
cell division cycle 25 homolog C (S. pombe) [Source:HGNC Symbol;Acc:1727]
Mouse Orthologues:
Cdc25a, Cdc25b, Cdc25c
Mouse Descriptions:
cell division cycle 25 homolog A (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:103198]
cell division cycle 25 homolog B (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:99701]
cell division cycle 25 homolog C (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:88350]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa39707 Nonsense Mutation detected in F1 DNA Not yet available
sa30807 Nonsense Mutation detected in F1 DNA Not yet available
sa39706 Nonsense Mutation detected in F1 DNA Not yet available
sa31237 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa39707
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
ENSDART00000109089 Nonsense 159 387 7 12
ENSDART00000109089 Nonsense 159 387 7 12
Genomic Location (Zv9):
Chromosome 1 (position 55268962)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 54051901
GRCz11 1 54729552
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACATTCTCTACCTGTCAATCACTTTGCAGGCCGCTGTGAGATTCCGT[C/T]AGCTGATGTCACAGCTGCAAGCCCCGCCCACACCTGTCACTCAGGTTGCA
Long Flanking Sequence:
ATCAAGTTTAACTTCTTTATTTCTACTGTGAAATCGTTCAAAAGCAAAGCAAAAAATCTGAGATGTGTATCAATTATTATAACACGTTTTTTGATTCCCGTCAATTCTTTAAATCATTAAATGTAGAAATGCTGTACACTATGTTTTACTATGTTTTGTGTATTTAATTAAATATATATATATATAACCCTTTCTTATACTAGTTTTTTATGCCTCATCTTTTATATTGTGCTGTATCCTGATGGTTTATGCAATAAAAAATAAATCGAAGTAAGAGATAAATAATCGAAGTAAGAGATTGCCGAATAAATACCTAGTAATGTCTATAAATTTATATTGACACAGTTTTCTATATTATTTTGTATGGTGGAGGTCTAACAAATCAAAATTGAAGCGAATTATTACATCCATGTGAATATGTGTAATTAACCACACTTTGTTATCCAATCATAAACATTCTCTACCTGTCAATCACTTTGCAGGCCGCTGTGAGATTCCGT[C/T]AGCTGATGTCACAGCTGCAAGCCCCGCCCACACCTGTCACTCAGGTTGCAGTTGCTGACCTCACGCTCATAGGAGACTTCAGTAAGGTTGGTTCTGCAAAATCACAACAATATAATGTATTATTACATGTTTATTTCAAAATTAAGATATTAATTACACAAGTCATTAGGTTCATCCATAGGAAATTGGTTTAAGCGTAAAAGTCAAGTGTGTGTTGACTTCCTGACTGACTCTTCCTTATTTTCCCGCTCTTTTCTTTTTTGTTTTCTTCATTATATCGATTTATTTTCTTTTTCTTTATTGTATTTTAATATTTTGTCAAGTTCACTTGTAATTTTTACACTGCTTCAGCTATTTAAAAAACCTCAGACTGCATTTTAACTTTAATTAATACACAGTGTAAAGTCATGGGGTCAGCAAGATGTTTATAAAAGAAAATAAGACCATATTTCAGCAAGGATGGATATATTGATTAAAACTGGCATTAATAATGTCAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30807
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
ENSDART00000109089 Nonsense 159 387 7 12
ENSDART00000109089 Nonsense 159 387 7 12
Genomic Location (Zv9):
Chromosome 1 (position 55268962)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 54051901
GRCz11 1 54729552
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACATTCTCTACCTGTCAATCACTTTGCAGGCCGCTGTGAGATTCCGT[C/T]AGCTGATGTCACAGCTGCAAGCCCCGCCCACACCTGTCACTCAGGTTGCA
Long Flanking Sequence:
ATCAAGTTTAACTTCTTTATTTCTACTGTGAAATCGTTCAAAAGCAAAGCAAAAAATCTGAGATGTGTATCAATTATTATAACACGTTTTTTGATTCCCGTCAATTCTTTAAATCATTAAATGTAGAAATGCTGTACACTATGTTTTACTATGTTTTGTGTATTTAATTAAATATATATATATATAACCCTTTCTTATACTAGTTTTTTATGCCTCATCTTTTATATTGTGCTGTATCCTGATGGTTTATGCAATAAAAAATAAATCGAAGTAAGAGATAAATAATCGAAGTAAGAGATTGCCGAATAAATACCTAGTAATGTCTATAAATTTATATTGACACAGTTTTCTATATTATTTTGTATGGTGGAGGTCTAACAAATCAAAATTGAAGCGAATTATTACATCCATGTGAATATGTGTAATTAACCACACTTTGTTATCCAATCATAAACATTCTCTACCTGTCAATCACTTTGCAGGCCGCTGTGAGATTCCGT[C/T]AGCTGATGTCACAGCTGCAAGCCCCGCCCACACCTGTCACTCAGGTTGCAGTTGCTGACCTCACGCTCATAGGAGACTTCAGTAAGGTTGGTTCTGCAAAATCACAACAATATAATGTATTATTACATGTTTATTTCAAAATTAAGATATTAATTACACAAGTCATTAGGTTCATCCATAGGAAATTGGTTTAAGCGTAAAAGTCAAGTGTGTGTTGACTTCCTGACTGACTCTTCCTTATTTTCCCGCTCTTTTCTTTTTTGTTTTCTTCATTATATCGATTTATTTTCTTTTTCTTTATTGTATTTTAATATTTTGTCAAGTTCACTTGTAATTTTTACACTGCTTCAGCTATTTAAAAAACCTCAGACTGCATTTTAACTTTAATTAATACACAGTGTAAAGTCATGGGGTCAGCAAGATGTTTATAAAAGAAAATAAGACCATATTTCAGCAAGGATGGATATATTGATTAAAACTGGCATTAATAATGTCAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39706
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109089 Nonsense 369 387 12 12
Genomic Location (Zv9):
Chromosome 1 (position 55260965)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 54043904
GRCz11 1 54721555
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGCGCCAGCGCGAATACAGGGAACAACTGAACAGCTTCCTCAGGAGA[A/T]GACAAACACGACAGCGCAGACGACGGCCAATCAGAAGACATCACAGAACA
Long Flanking Sequence:
CTCCATAACACTACGCTGAAGGATTTCAACAGTCAAAAATCACATTAAAACACAACTGAAGGCTTTAAATGAGATGTGTGAGAAACCAGTGCTACACTGGAGTAGTTTGAGGACGAAAACCTGACTGAAATACAACATCTGAACTGCCGTTTTAGCTGTGGTATCCATATACGCAGAATAAAGCACTCCAGTCCATTGTATTATTGGAAAATAATGCACACCTGAGGCATAACGGCCACTCTGCTTCTAGTTATACATTCTAAATATATTAATTCAATTGTTGTCAATAACTTGTTATGTATCTAATGTCTAAATGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGTGCACAGGATTTGTGTGATCCGTGCGGTTATGTGTCCATGCGCCAGCGCGAATACAGGGAACAACTGAACAGCTTCCTCAGGAGA[A/T]GACAAACACGACAGCGCAGACGACGGCCAATCAGAAGACATCACAGAACAAAACGATAAACATTCTGATCATACCCTGCCAATCGGAAGAGGACAGGAACTGCATCATGTTTGTTCTGTGTAAAAAAATTGCATACCACTATTTATTTGATGACCAAAACTGCATATGTTAAGGTGGACGTGAGTAGCTACATACTTTTTGGTCGTGGTGAGTGAATGAATGTGAGTCTAAAATTATTTTATTTATATTAGTCAATGTTAATATAATTAATTACATAAATTTATTTTAAAAATCATGATTTAGTCAATGAGTTAAGCATGTGCATTTGATTAATGTGTTCTTTTTATAGTTAAATTCTATTAAATAGCTTGCTGAAATGAAGACAATATTATTTATTAGCCTTTTTATTTAGAATTTAATAATTAATTACATTTTTATAAAGATATTAAAGGCAGAACCTCCACTGAGAAATGTAGTATCAGTGCCTTTCTGGGTGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31237
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109089 Nonsense 376 387 12 12
Genomic Location (Zv9):
Chromosome 1 (position 55260944)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 54043883
GRCz11 1 54721534
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAACAACTGAACAGCTTCCTCAGGAGAAGACAAACACGACAGCGCAGA[C/T]GACGGCCAATCAGAAGACATCACAGAACAAAACGATAAACATTCTGATCA
Long Flanking Sequence:
GATTTCAACAGTCAAAAATCACATTAAAACACAACTGAAGGCTTTAAATGAGATGTGTGAGAAACCAGTGCTACACTGGAGTAGTTTGAGGACGAAAACCTGACTGAAATACAACATCTGAACTGCCGTTTTAGCTGTGGTATCCATATACGCAGAATAAAGCACTCCAGTCCATTGTATTATTGGAAAATAATGCACACCTGAGGCATAACGGCCACTCTGCTTCTAGTTATACATTCTAAATATATTAATTCAATTGTTGTCAATAACTTGTTATGTATCTAATGTCTAAATGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTGTGCACAGGATTTGTGTGATCCGTGCGGTTATGTGTCCATGCGCCAGCGCGAATACAGGGAACAACTGAACAGCTTCCTCAGGAGAAGACAAACACGACAGCGCAGA[C/T]GACGGCCAATCAGAAGACATCACAGAACAAAACGATAAACATTCTGATCATACCCTGCCAATCGGAAGAGGACAGGAACTGCATCATGTTTGTTCTGTGTAAAAAAATTGCATACCACTATTTATTTGATGACCAAAACTGCATATGTTAAGGTGGACGTGAGTAGCTACATACTTTTTGGTCGTGGTGAGTGAATGAATGTGAGTCTAAAATTATTTTATTTATATTAGTCAATGTTAATATAATTAATTACATAAATTTATTTTAAAAATCATGATTTAGTCAATGAGTTAAGCATGTGCATTTGATTAATGTGTTCTTTTTATAGTTAAATTCTATTAAATAGCTTGCTGAAATGAAGACAATATTATTTATTAGCCTTTTTATTTAGAATTTAATAATTAATTACATTTTTATAAAGATATTAAAGGCAGAACCTCCACTGAGAAATGTAGTATCAGTGCCTTTCTGGGTGTTTTAAGGGACATTAGTAAAATCTT
Associated Phenotype:
Not determined