ZMP
cdc5l
Ensembl ID:
ZFIN ID:
Description:
CDC5 cell division cycle 5-like [Source:RefSeq peptide;Acc:NP_957378]
Human Orthologue:
CDC5L
Human Description:
CDC5 cell division cycle 5-like (S. pombe) [Source:HGNC Symbol;Acc:1743]
Mouse Orthologues:
Cdc5l, Gm9049
Mouse Descriptions:
cell division cycle 5-like (S. pombe) Gene [Source:MGI Symbol;Acc:MGI:1918952]
predicted gene 9049 Pseudogene [Source:MGI Symbol;Acc:MGI:3644216]
predicted gene 9049 Pseudogene [Source:MGI Symbol;Acc:MGI:3644216]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22983 | Essential Splice Site | Available for shipment | Available now |
sa22984 | Splice Site, Nonsense | Available for shipment | Available now |
sa16815 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22983
Status:
Available for shipment
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:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064313 | Essential Splice Site | 301 | 468 | 7 | 10 |
ENSDART00000121806 | Essential Splice Site | 301 | 801 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 4847647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 4921718 |
GRCz11 | 17 | 5079833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGAGTTCACCAAGAAGAGGAGCAAACTAGTGCTGCCGGCACCACAG[G/A]TCAGAGACAAGCTCAGATAATTAACACATTAAACACTAAACAGCTACCAG
Long Flanking Sequence:
AATTTGAATTGATTAATATTCATTTATAGAATCCCAATTTCTGTTTAACGGAGAGAAGATTTTTTTTCAACACGTTTCTGAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACGGTAAATAATATTTGACTAGATATTTTTTAAGAAACTTCTATGCAGCTTAAAGTGACATTTAAAGGCTTAAACAGTGGTTTGTTCTGTAGACAATTTAAAAAAAAAATTGCTTATGGGGGCTCATTTTTTTGATCCACTTCAGATGTTGATTACTGTATATAGTAAAAAGCACTATAGAAATAAAAATGAATTAAATTAAATATTGTCTGTAGTGAAAAGGAGGATCGTGACCGAAAGAAGGACAGGCAGAAGATCAAGAAGAAGAAGGAGTCTGATCTGCCCTCAGCTATTCTGCAGACCAGTGGAGTGTCAGAGTTCACCAAGAAGAGGAGCAAACTAGTGCTGCCGGCACCACAG[G/A]TCAGAGACAAGCTCAGATAATTAACACATTAAACACTAAACAGCTACCAGATTATTTTACAGGGTTTCCACACTTCTTGAAAGTACTTTAATTTCAGACATAAGTATTTAAAGCCTGGAAAGTACTTAAACACAGGTCCTTGAATTAAATTTGAAATGAAATGTATGGTGTTATTTCAGCAATTGTATTGCACTTCTGTCAAAATCAGCACCAAAGAATTATAAAATATTCATTTAAAAATCATACATTTAAGTCTTGTACAAGATCTGACAAATAATGCACATTTTATCAATATTTCAGAAACCACATTTGAAAATTACCAGTATTGAATTTAACAAGTTCTTTGAACATGACTGTTTAAAATGTTTTTATCAACATTTTTGACAACGACACATTCAAAACATTGTCATTACTCTGGCTTTTCAATGTAAATATTAAGTGTAAGTGGCTTTCATGGCTGTGCTTCATTTGAAAATATTGGTAAAATACTGTTCATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22984
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064313 | None | None | 468 | None | 10 |
ENSDART00000121806 | Splice Site, Nonsense | 523 | 801 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 4858758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 4932829 |
GRCz11 | 17 | 5090944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGGACGAGAGCTTTGTGGAGGACGCGGCTGAGATCGAACTGCGTAAA[C/T]AGGCCAGTTAACCTCTGCAAACACACTGATGTTCATGAAGTGATCGCTGG
Long Flanking Sequence:
CAAATACAAATACAAATACCGGCTGCTCCGCACATCCCTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATAAATATCGCAATATATATCGCAGGGAAAAAATTTTCCAATATCGTGCAGCCCTACCCCAAACACAAAATCGAGCCTGCAAACACAAATGCAAAAAAAAAAAGGTTTATTTGAGGCCTCTTCTCCAAATTTTGCTCCCTAAAATGCCATATCTGCATGTTTATTTTTCTGCACGTATTTGCTATCAGTGTGGTGTTCCTGGATGGTTGTGTTCTGTGTTTTCTCCAGCAAAGAGAGTCTCGTGAGCATCTACGACTGGGTCTGATGTCTCTGCCGGTGCCCAAAAATGACTTTGAGATCGTTCTTCCTGAAAACGCTGAGAAAGAGCTGGAGGAGACGGAGGTGGACGAGAGCTTTGTGGAGGACGCGGCTGAGATCGAACTGCGTAAA[C/T]AGGCCAGTTAACCTCTGCAAACACACTGATGTTCATGAAGTGATCGCTGGCTGTCCAGACGTGCTGCGTTTGGTGTGTGTCTGCCGGTATTTATCTTGTGTGATATTTTCCACAGGCTGTCAGAGATGCTGAGAGGGAGAAAGAGCTGCGCCAGAGACACACATCGGTTCAGAGAGATTTACCAAGACCTTCAGAAGTGAGAACACACACACACACACACACACATCCTTGTGTATCTGTCCAAACAGTGGTGTTATAGGTAACTAAAAGTACATTCAAAATTTTATAGAGTTGAAGTCAGAATTATTAGCCCCCCTGAATTATTAGTCCCTGTTTATTTTTTACCCAATTTCTGTTTAACGGAGAGCAGATTTTCTCAACACATTTGTAAACATAATAGTTTTAATAACTCATTTCTAATAACTTATTTATTTTATCGTTGTCATGATGACAGTAAATAATATTTGACTTGATATTTTTCAAGACACTTCTATACAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16815
Status:
Available for shipment
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:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064313 | None | None | 468 | None | 10 |
ENSDART00000121806 | Nonsense | 708 | 801 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 17 (position 4869040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 4943111 |
GRCz11 | 17 | 5101226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTATTTYTCCATCAGATGAACCGTGGCCAYATGACGGCGGAGGCGAAG[C/T]GAGCAGCRAAGATGGAGAAGAAGATGAAGATCCTGCTGGGTGGATATCAG
Long Flanking Sequence:
TCCCTAGGTAGGCATTCAAGAGGCATCCGATACGGATGTCCAAGCCATCTCAGCTGACTTCTCTTGATGTGGAGCTCCTCCAGGGTGACAGAGCCCCTCACCCTATCGATAAGGGTGCGCCCTGCCACTCTGCAAAGGAAACTCATTTTAGCCGCTTGTATTTGAGATCTTGTCCTTTCCGTCATGACCAAAAGCTCAGGGCTATAGGTGAGAGTAGGAACGTAGATTGACCGGTATATCGAGAGCTTTGCCTTTCGGCTCAACTCCTTTTTTACTACAAAGGACCAGTACATTGACCGCATTACTGCTGCTGCTGCTCTAATCCGCCTGTCAATCTCTCGTTCCATCCCTCCCTCCCTCACTCATGAACAACACCCCAAGCTACTTGAACTCCTCCTGGGGTCTTTGTTGTTTTTTAATTTATAATTTCTTGATTACAATTTTTCTCCTCTGTATTTTTCCATCAGATGAACCGTGGCCACATGACGGCGGAGGCGAAG[C/T]GAGCAGCAAAGATGGAGAAGAAGATGAAGATCCTGCTGGGTGGATATCAGTCGAGGGCGATGGGCTTGCTGAAGCAGCTCAGTGAAGTGTGGGATCAGCTGGAGCAGGCCAACCTGGAGCTGCACACCTTCATGGAGCTTAAGAAGCAGGAGGATCTGGCCATCCCACGCAGACAAGAGGTGCGCATATACACACACACACCACACTCTGGCCATCCCACGCAGACAAGAGGTGCGCATATACACACACACACCACACTCTGGCCATTCCACACAGACAAGGGGTGCACATATACACACAAACACCACACTCTGGCCATTCCACACAGACAAGGGGTGCGCATATACACACACACACCACACTCTGGCCATTCCACACAGACAAGAGGTGCACATATACACACACACCACACTCTGGCCATTCCACACAGACAAGAGGTGCGCATATACACACACACCACACTCTGGCCATTCCACACAGACAAGAGGTGCGCATATACA
Associated Phenotype:
Not determined