ZMP
ENSDARG00000063721
Ensembl ID:
Human Orthologues:
CDK16, CDK17, CDK18
Human Descriptions:
cyclin-dependent kinase 16 [Source:HGNC Symbol;Acc:8749]
cyclin-dependent kinase 17 [Source:HGNC Symbol;Acc:8750]
cyclin-dependent kinase 18 [Source:HGNC Symbol;Acc:8751]
cyclin-dependent kinase 17 [Source:HGNC Symbol;Acc:8750]
cyclin-dependent kinase 18 [Source:HGNC Symbol;Acc:8751]
Mouse Orthologues:
Cdk16, Cdk17, Cdk18
Mouse Descriptions:
cyclin-dependent kinase 16 Gene [Source:MGI Symbol;Acc:MGI:97516]
cyclin-dependent kinase 17 Gene [Source:MGI Symbol;Acc:MGI:97517]
cyclin-dependent kinase 18 Gene [Source:MGI Symbol;Acc:MGI:97518]
cyclin-dependent kinase 17 Gene [Source:MGI Symbol;Acc:MGI:97517]
cyclin-dependent kinase 18 Gene [Source:MGI Symbol;Acc:MGI:97518]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11008 | Essential Splice Site | Available for shipment | Available now |
sa18935 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44696 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38718 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11008
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103073 | Essential Splice Site | 80 | 382 | 2 | 11 |
ENSDART00000103073 | Essential Splice Site | 80 | 382 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 341632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 5391 |
GRCz11 | 9 | 201566 |
KASP Assay ID:
2260-1320.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTGTACGAGTGCGCATGCGTAACCTACATCAGCGCATCTCCAATGAGG[T/G]AAATCACACTGTTKTACTCACASAGACGCACACAGACACATRCCAGATGA
Long Flanking Sequence:
AATGAGATGGAGAGATGGACACTAGTGGGCGGGGCTTTCCCCCTCTGATGACACATACAAAGGGAGAATGTCAATCACAGTGTTTCTGCATCAAGTCTGATTAATTAATGTTGATTATTAGAGACTGCTGGAGATACTCACACACTGCTGGATTATAAAGGTGATTTCTGCATAATAGGTGTCTTTTAAATATGGATCAGTGGTCTGCAAGTGGTTTTGATGGTCTCTTTAGCACTCTTTGTTGACTGCACTGCTGTTCTTACTTAATGACTACTTAATTACTCAATCTACAATAAGTATAACAGTACAAATATAACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACAGAGGTCACCCATGGTAAAATGGGGTCAGATGGGGAAAGTGATCAGGCTTCAGGAACATCCTCTGATGAAGTTCAGAGTCCTGTACGAGTGCGCATGCGTAACCTACATCAGCGCATCTCCAATGAGG[T/G]AAATCACACTGTTGTACTCACAGAGACGCACACAGACACATACCAGATGAGTATTATGTAGGTGATTGTGTAAAAGCCAGTTCTGAACAGTCTAAATCTTCTACATCGAGCGGTTATTACCTGATCATCATGTGGAAGACTCTTTTCACTGGGAAACATGCGTATCTTACAGTTTTTGTCTTGTTTTTACTTCAAATATTCTTAAATCAGTCAGCATTTTCCAGACCAGCACAGAATATAGTGTTGTGTTCAGCAATCATGAGTCAAAATGAAGAGAGTTTCTCCTGAAAACAAGCAGAATATATAAAATAGTGTCATTTCAAAGCAAAAACACGATTATTCTGCTCACTTCAGTTTAACTCATTATTGCTGAATATATATATATATATATGTGTGTGTATTTTATGTGATTAAATGTTTATTGATTGTACATGTGAGTGGTCACAGCATGTTTACATGATCTTACCAATAAACAAAACAAGATCCACTCCTCAAGCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18935
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103073 | Essential Splice Site | 80 | 382 | 2 | 11 |
ENSDART00000103073 | Essential Splice Site | 80 | 382 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 341632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 5391 |
GRCz11 | 9 | 201566 |
KASP Assay ID:
2260-1320.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTACGAGTGCGCATGCGTAACCTACATCAGCGCATCTCCAATGAGG[T/G]AAATCACACTGTTGTACTCACAGAGACGCACACAGACACATACCAGATGA
Long Flanking Sequence:
AATGAGATGGAGAGATGGACACTAGTGGGCGGGGCTTTCCCCCTCTGATGACACATACAAAGGGAGAATGTCAATCACAGTGTTTCTGCATCAAGTCTGATTAATTAATGTTGATTATTAGAGACTGCTGGAGATACTCACACACTGCTGGATTATAAAGGTGATTTCTGCATAATAGGTGTCTTTTAAATATGGATCAGTGGTCTGCAAGTGGTTTTGATGGTCTCTTTAGCACTCTTTGTTGACTGCACTGCTGTTCTTACTTAATGACTACTTAATTACTCAATCTACAATAAGTATAACAGTACAAATATAACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACAGAGGTCACCCATGGTAAAATGGGGTCAGATGGGGAAAGTGATCAGGCTTCAGGAACATCCTCTGATGAAGTTCAGAGTCCTGTACGAGTGCGCATGCGTAACCTACATCAGCGCATCTCCAATGAGG[T/G]AAATCACACTGTTGTACTCACAGAGACGCACACAGACACATACCAGATGAGTATTATGTAGGTGATTGTGTAAAAGCCAGTTCTGAACAGTCTAAATCTTCTACATCGAGCGGTTATTACCTGATCATCATGTGGAAGACTCTTTTCACTGGGAAACATGCGTATCTTACAGTTTTTGTCTTGTTTTTACTTCAAATATTCTTAAATCAGTCAGCATTTTCCAGACCAGCACAGAATATAGTGTTGTGTTCAGCAATCATGAGTCAAAATGAAGAGAGTTTCTCCTGAAAACAAGCAGAATATATAAAATAGTGTCATTTCAAAGCAAAAACACGATTATTCTGCTCACTTCAGTTTAACTCATTATTGCTGAATATATATATATATATATGTGTGTGTATTTTATGTGATTAAATGTTTATTGATTGTACATGTGAGTGGTCACAGCATGTTTACATGATCTTACCAATAAACAAAACAAGATCCACTCCTCAAGCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44696
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 |
---|---|---|---|---|---|
ENSDART00000103073 | Nonsense | 148 | 382 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 344708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 8467 |
GRCz11 | 9 | 198490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTAGGGCACATACGCAACAGTGTA[T/A]AAGGGTCGCAGTAAGCTAACAGATAACCTGGTGGCTCTGAAGGAGATCCG
Long Flanking Sequence:
GGACAAACTGGGAGAGGTGAGACCCGGACACGCTCACATCTGGCTGTGCTGGCATCTTTGCTTTGGTCATACTGATGATGTCAGACTCATATTACAACACATGAAAACCACCAGTAATGCCACTGAGCATCAGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGGCGTGCATGCGTATACGTGTGTGTGTGTGTGTGTGAAGGCTGCAGTTATGAGTATTGCACAAAACAGCTGAAAGTCTGGAGACAGTGATGTTGTTTTTCTACTCTCCTAAATCTGCTGGGTTATTTCAGCCCAGTTCTGGGTGTAATACAGACTAATAACCCAGCATCACTTACAGTGTTTATCCTTCAGTGTGAAGTGTTGGACAGCTAAACAAACCCTTCACAGCTGTGTTTCTGTTCACATCCAGAGTGTTTGGATTCTGAATGCTTTGTCTACTGTATATAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGGGCACATACGCAACAGTGTA[T/A]AAGGGTCGCAGTAAGCTAACAGATAACCTGGTGGCTCTGAAGGAGATCCGGCTGGAGTATGAAGAAGGCGCACCCTGCACCGCCATCAGGGAAGGTAGAGCTCTAGCAGACACTCAGCGGAAGCGCTGCTCTGAACAACACTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGAGCTCTCACAGACTTTATGATTGATTTCTCAACAGTTCTGGGTCGTCTATCTGTAATGCTGTTTATTTATTTTATATTATATAGTTATCAGTATTTAAATTGACTGTGTGGTTAATAGCTGAAATAATTGTAATTTTGGGAATGTTCTGCTCTGGTCCTCTATCAGATCATCATCATTATTGTAATGGCTCAGACTGTACATTGCTGATCTGCTAACACTGCTGTTCTTACTCACAGTTTTGTTTCCAGTGCAAACATCTACAAACACTTCAATCAAGAAGCATTGTGTTTATTGTGTATCGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38718
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103073 | Nonsense | 277 | 382 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 348649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 12408 |
GRCz11 | 9 | 194549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCAGAGTGTTGGTGTTCATGTAAACACACTGATTGTGCAGGTCTCGCC[C/T]GAGCCAAGTCGGTCCCCACAAAGACGTTCTCTAATGAGGTGGTGACGCTG
Long Flanking Sequence:
GGTGTTTACATGAGCTGCTTTAATAATGTTCCTTTCATGATCTCGTTTTACATGTTACAGCACATTCACACATCCATTACCGTCATTGCCTCAGCATTTGATGCTTGTTTCCTCTGGTGTTTCACACAACTGCTTGTGTTCGTCATGGCACCATCGCATGGGATTTGGGGCGTTTTAACTGCAGTTAAATTTGCGTAAAACATTAGCGGTTAAGACATTAACATTTACATTAACTGCAGTTACATTTGTAGAATTAGAAGTAGAATAGGTTGACTGCGGTGTCTCCATGTCTGAACTGCTCTTCAGTAATGCACACAGGATTCACAGGATTACTCCACGTCTTCCTTCATTTGTGTTTAGTTCCATCAGGACTTTAGTCTGATTCCGGTCATCAAAGCTCTCTGTTCTCATGGTGGACTCTTCATCAGTGTATTGTGTTAAAGTTGTTCAAGTCAGAGTGTTGGTGTTCATGTAAACACACTGATTGTGCAGGTCTCGCC[C/T]GAGCCAAGTCGGTCCCCACAAAGACGTTCTCTAATGAGGTGGTGACGCTGTGGTACAGACCTCCGGATGTGCTGCTGGGGTCCACAGAGTACTCCACCCCCATCGACATCTGGTGAGAGACACATCCACATGGATATATTCGGTCCAATTGTAATTGAAACCAATTGAAACCAGGCATAATCCAGCCATCTGTTTTAAACTACCCATATTACCAGAATATAACAGAGATATGATCACGAGCTCTACATTGTGGGCACCTGCTCTCCATATTCTGCTGCTTTCAGTCTTTTAAGCCCTCACGTCTCTGTCAGAGCTGCTGAGATGTTTACCTTTATCTTGTGGATATTGCTCAGAGATTCAGCCATTAGTTTCTGCTTTTATATGTAGTGTCGGTTTGTTTTGCTTAGATTAATATTAGCTGGTTATGAACATCTGCTCCTTCACCTCTTGCTCACTCTGCACTTCAGTTTATACTTTAATCACACCCAATAGCGGGACGC
Associated Phenotype:
Not determined