ZMP
cdk16
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate PCTAIRE protein kinase 1 (PCTK1) [Source:UniProtKB/TrEMBL;Acc:B0
Human Orthologue:
CDK16
Human Description:
cyclin-dependent kinase 16 [Source:HGNC Symbol;Acc:8749]
Mouse Orthologue:
Cdk16
Mouse Description:
cyclin-dependent kinase 16 Gene [Source:MGI Symbol;Acc:MGI:97516]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14702 | Nonsense | Available for shipment | Available now |
| sa41122 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14702
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 |
|---|---|---|---|---|---|
| ENSDART00000093388 | Nonsense | 126 | 524 | 3 | 16 |
| ENSDART00000132700 | Nonsense | 71 | 184 | 3 | 6 |
| ENSDART00000137382 | Nonsense | 126 | 524 | 4 | 17 |
The following transcripts of ENSDARG00000032072 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 8954662)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 8371244 |
| GRCz11 | 8 | 8409829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGCGATCAGGCTTCGGCCAMGTCCTCCGATGAGGTGCACAGTCCCGTC[C/T]GAGTTCGWCTGAGAAACAACCCCGGTCGCAAAATTTCCACWGAGGTATGT
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGGAAAGGAGCGAGGGGGTGGGAGGTTGTGTTATGGTTTAATAGGGGGGATGGGATGGGGAGTGAATAAATGAGAGTGCAAGATAATGACTTCTATTTTTTTTCCTTTTGTGTGGGTATGAGACGGATCTCCTTTCAGAGCAGCTAAGTAGTTCCTCAGCAGAGCAGTAGTGTGGTATGAATCTCCGAGCCATATAAACGCTTTATAAAAGTGTTGCAGACTCACAAGATAATACATCAGCATCACTTTGATGATTTAAATTAGAATTGTTATATTTAATTTAGTCAACATTAGCAGCATCATTAGAATAGTAATGTCAGCATAGCATGCCAATGTTTTTGTGTGTGTGTGGTTGTTGTCTCTAAATGCAGAAATCGTCCATGAGGATGTAAAAATGGGTTCAGACGGAGAGAGCGATCAGGCTTCGGCCACGTCCTCCGATGAGGTGCACAGTCCCGTC[C/T]GAGTTCGTCTGAGAAACAACCCCGGTCGCAAAATTTCCACAGAGGTATGTTCAGGGTTCTGATGTGACACTATTTTTAGAGCTGTGAATAATACATGATGTGTTCGGGTTATAAAAACATGTCGTTTTTCGTAGCTTACCTTTGTTTTTGTTTTGCTTGCTTGGATTAAAGCGTGTACCACATAATAGCCATTAGCTTTTTTTCATGCTATTGAAGTTACATCAGTTGTGCGTGACTAATGGTGCATTGTGGGTACTGAAAATGCTCCACGGCATGGTACCCATCAGTTAGATGACTAGCCTGCGGGCCAGATGGGTTATTACTCCTATGGAGTGTAACGAAAGCTTTAGGCCTTAACTAATAATGGTCCCCCCACTCTCCTGCTTTACTCTCAGGACATAAACAAGCGTCTTTCTCTGCCTGCCGATATCAGGCTTCCTGATGGCTACCTGGAGAAATTCAGCCTCAACAGCCCTCTGTTTGACAAACCGCTCAGCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41122
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000093388 | Essential Splice Site | 201 | 524 | 5 | 16 |
| ENSDART00000132700 | Essential Splice Site | 146 | 184 | 5 | 6 |
| ENSDART00000137382 | Essential Splice Site | 201 | 524 | 6 | 17 |
The following transcripts of ENSDARG00000032072 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 8947467)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 8364049 |
| GRCz11 | 8 | 8402634 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGATTTGGGAAGCTGGAGACGTACGTGAAACTGGATAAACTAGGAGAG[G/A]TAACGTTAGCATCTGTTATACACTCCATCACAAAACACCATTCACTCCAC
Long Flanking Sequence:
AAGTTTTTTTTTCTTTAATAATGAAATATGACTCTTGAAAGAAGGTCAAGATTGTTCTTAATTCATTATCATAAAGTAGCTCGACTTCAGTTTGCCCTTGATGTGACATATAAACCCAGAACGTGATGTTTATTCAGTGCTGTTGACGCACGCTTGATCTGTGATGCGTTTAAAAACACTTTATTTGTTACACTTCAGTTGTTCCCAATTTATTTTTAGGGAGAGCTGTTTAAGCTCATGTTTTCAGCAGGCATTATATAAACCTTTATGACCAGCCCAGCACATCACATCCGTCTGAAACGGGAGCAGGGCAATTTTGGATGCTTTCTAATGAGTTCACATGAATGCCTTTGAAATTTTCTGCCCTGTATCCTAGTGTTGTTTTAGTGCTGCTTTTTAGGAGCACACAGTTATTGACACAGTTTTTGTCTTTGTTTGAGCAGTCTGAGATCGGATTTGGGAAGCTGGAGACGTACGTGAAACTGGATAAACTAGGAGAG[G/A]TAACGTTAGCATCTGTTATACACTCCATCACAAAACACCATTCACTCCACATATTAAGACTTCTATAGCTTAATATGATATAAGGATCAGTCTTAAAGGGATAGTTCTCCAAAAACCGAAAAGACTGCCATCATTCACTCGCTATATGCATGTTTCAAACCTGTTTGACTTTCTTTCTTCTATTGAACACAAAAGAAGATACTTTGAAGAAAGCTGAAATCCTGTAACCACAGACTTTCATAGTATTTGTTTTTTCTATTATGGAAGTCAATGGTTACAGGTTTTCAGCTTTCTTCAAAGTGTCTTTTTTTGTGTTGAACAGAATAAATAAACTTATAAGGGTTTACAACCAGGGCTTTACATTAACTTTTTTAATCACCGGCCATTGTGGCTAGTAGTTATCCAATGTTACTAGCCACTCTGCATTTTCACTAGCCACAATTTTGTTGTTGGGAAAATATATTTTACATGCATAAATTTGACGTTGACATGCTAAAATT
Associated Phenotype:
Not determined