Busch Lab

ZMP

ENSDARG00000063721

Ensembl ID:
ENSDARG00000063721
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]
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]

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
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.
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