ZMP
cdc25
Ensembl ID:
ZFIN ID:
Description:
cdc25 [Source:RefSeq peptide;Acc:NP_001108567]
Human Orthologues:
CDC25A, CDC25B
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 B (S. pombe) [Source:HGNC Symbol;Acc:1726]
Mouse Orthologues:
Cdc25a, Cdc25b
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 B (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:99701]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42163 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42162 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42163
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000020576 | Nonsense | 84 | 563 | 2 | 15 |
ENSDART00000082393 | Nonsense | 84 | 562 | 2 | 17 |
ENSDART00000142785 | None | None | 122 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 14789389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 14797384 |
GRCz11 | 13 | 14928376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCGTTTTGATGCAGTCAATGTGAAACTCCAAAGCGGAAGAAAAATT[T/A]GCCCCTCCTGAAGATTCCTTCCTTCGCCTCTGATGCCTCTTCTGATGCAG
Long Flanking Sequence:
GACGATCCACGATCTTCTTCAAAAATGGATATTGATATGGTTCCAGGCGACGTTAGCCCTGTTTATGATCCATTCAGCACTGGGCCCGAATCAGCCCTCGGAGCTCCCCGCTTCACTCTGCCGGAGCTCGGTGCTCGGGGCTCCCCCTGCATGAAGAGCCTGGCCTCTCCCGGGCCCATGGCGGTGCTGTCTCCTGTCACCAACCTGGCCCTCAACATGAATAATCTCGCTGTTCTTGGAGGGTGAGTGGAGCTGGGCTGTTTTTTTCAAGATTGGAAAAATAAATAAAACAACTGCATCGCTGCAGAAATACTTCCTGGAACAGTTTGCAGGCTGTTTACATTAATGACGCTAACGTACCTTATCTATTTGTGTAACTTGGTGCTTTAACGTTATATGAGGCGAAAACAAACATGATGCAATTCATTTTCGTTTCGCTAAAAAGTTTGTTTTCTCGTTTTGATGCAGTCAATGTGAAACTCCAAAGCGGAAGAAAAATT[T/A]GCCCCTCCTGAAGATTCCTTCCTTCGCCTCTGATGCCTCTTCTGATGCAGGTTAGCTTGGTGTACATGAGTGTATTTTTCTGTGAAACTACATATTGTATGTATATGGCAGGCTGCTTTAAACTCGTATTCCATTATCTGGTATTTATCAATTAGCAAGTAGTCCACCAAAATATCTATATAAATAAAAAAACATAACTTGCATTGCCTGCGAGTATGATGGAATGGCAAAAAAAAAAAATAGTTGATGCTAAACGTTAGGAGGATAAATGTTATGTTAGCGCTCAGCCCTTAAACGCATAGTTTACCCAAACATTAAAATGTACTCCTCATCAAATGGTTCCAATCATTTTGAGTTGCTTTATTTTGTTTAATGCAAAAGAGGTTTTGGCGAAGAGAGAACAAATATTTAATTTTTTAGCTACTGAATAGCATAGTCTAATAATGCATATTTAGACAGTAGTAGCATTCACGGTCATGTAAACAACTTTGCTAAATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42162
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020576 | Nonsense | 287 | 563 | 9 | 15 |
ENSDART00000082393 | Nonsense | 286 | 562 | 11 | 17 |
ENSDART00000142785 | None | None | 122 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 14782658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 14790653 |
GRCz11 | 13 | 14921645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAATGGACAGTCTTCTAACTGCTCCTCTGGTGGCCAAGCAAATTCCT[G/T]AAACTGATTCGGTATGTTGTTAAATTGATTTATTTCTAATTTTTTTTTTC
Long Flanking Sequence:
AGTAATAGCCTTCATTAACATAAATCAATAACAGAAAAGACGATCACAATTAAACCTGCCTGAAGAATAGCGTTTAGTTTATTTATTGGTTGTAGTCAATGTTTTCAGTAATTTGACTTCATAAGGCTAGTTAGTTTGCCTAGTAGTTTTTTAAAGAAATATTAATTTTACGTTGTGGTGGTGTTTTTAGCATAGCCTGTGAGAAATGAAGGAACAACGAAAGTTGAAAGAATTGACCACCATGGACCAGTATTAACAATTCTTAACACTGAGCTTGAAGTTTAAAAAAAAATAAAAAATAGTTAAATGACAATTTTATTGAAAGCATTTTTTTGTCATCAAGTATTTAACTTTTTTAGAGATGCTGTATTTAAGGTAGAAATTTTTAGTATCTTCACAGTACTATGGTCTTTTTTTTTTTTTTTTCTCAGAATGACTCTGAGGTTCCTCTGGGAATGGACAGTCTTCTAACTGCTCCTCTGGTGGCCAAGCAAATTCCT[G/T]AAACTGATTCGGTATGTTGTTAAATTGATTTATTTCTAATTTTTTTTTTCAACCCTATTTTTTTTAAACAAACATTATATTTTTTTATGGTTATGACATGATTGTAATGACCAAATCCATTTTGATTACCTGTAGCCTGTCATTCGCTGTCGTCCACGTGGGTTGTTCAGATCTCCATCTATGCCCTGTGCAGTCGGGCGCATCCCGCTCAAAAGACCTGAAAGACCACAAGATGAGAACACGCCTGTCCGAGTGAAGAGGAGACGGAGTCTGGCAGGGACACAAGTGTCAACCACAGAGCAGGAGGATGTTGTACATCAGGTCAGAAAAAGAGAAAATAAATGAATGTCTTTATTATGGTGCTGATGAGTGTGTTTGGTTTGAGTCCTGATTTTGTTTTTTTTATCTCCTTGTAGGTTCAGAGGTCCAAGTCCTTTAATCACTCACAGATTGAAAGAATGTTGGACACCGATCCTAGTAATGTGATTGGAGATTTTACC
Associated Phenotype:
Not determined