ZMP
cdk12
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens CRKRS, Cdc2-related kinase, arginine/serine-rich (CRKRS) [Source:
Human Orthologue:
CDK12
Human Description:
cyclin-dependent kinase 12 [Source:HGNC Symbol;Acc:24224]
Mouse Orthologue:
Cdk12
Mouse Description:
cyclin-dependent kinase 12 Gene [Source:MGI Symbol;Acc:MGI:1098802]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1307 | Nonsense | Available for shipment | Available now |
sa29141 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23419 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1307
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093402 | Nonsense | 250 | 1293 | 1 | 14 |
ENSDART00000143222 | Nonsense | 102 | 688 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 5482053)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 4941364 |
GRCz11 | 19 | 4857850 |
KASP Assay ID:
554-1222.1 (used for ordering genotyping assays)
KASP Sequence:
AGYGTGCGTTCATCCAAATCTCGCAAAGAAAAGAGAAGGAACGAGGAGTA[T/A]GAGGAGGMCCGGAGCCATCGAAAGGCCGCAAAGAGTCGCAAGTCTAGCCC
Long Flanking Sequence:
GTGGAGTACGACGACATCAGCTCGGATTCGGACACGTTCCTTGACTCCCCCGCCACCGGGAACCCGGTGGACACCAGAGACGCCGAACAGCTAGATCTGTCGGACTACGGTGAGGTGGTGGCGGGGGTCGCCAAAGAGAACCGGACTCATAAACGCAAGCGCTCCCGGAAGAAATCCAAAGACCGGCATCGGGTCAGGGAGTCTGCGGAAAGACCAGTAGGGGCCAAAAAGAGCATCAAGGACCGGGAGAGGGTGAGCAAAGAGAGCCGAAAGAAGGTTAAGGAGAGGGCTAGTCCAGTCGCGTGCCTTGCTGCTTCATCATCCAGACGCTCCGGTGAGACCGGTGCCAAAAAGCTCGGCGGCGGCGAATCGGTGTCCTCCAGCGCGGTGCAGTCAGCTGTCAGCCTGGGCAGCAGCGCCTCCTCCGCATCTTCCTCCATCAGTAAGGAAAGCGTGCGTTCATCCAAATCTCGCAAAGAAAAGAGAAGGAACGAGGAGTA[T/A]GAGGAGGACCGGAGCCATCGAAAGGCCGCAAAGAGTCGCAAGTCTAGCCCTAAAGGGAAAAGCCAGTCCCGGAGGACCGTGGTGGACAGTCCTTCCGTTGCGGAGCTCGAGAACAGTTACTCCTCCAAACGCAAGGCCGCGAGCCCGAGCCCGTACAGAGAGCCGCCCAGGCGGAGCAGACAGAGGTCCGAGAGCCCCTACGGGAGAAGGAGGTCTTCCAGCCCTGAGAAGGATGGGAGTCCGTATGTGAGCAGAAAACACTCACCTGGAAGTCCTTACGCGAGCAGACGCTCACCCAGCAGCAGTCCAGTGTCCAGGTGTGTGCTCACTACATATTAAACGCACAGTTCACCCTAAAATTATAACGCTGTCATCATTTACTCACCTTTTACTTGTTTCAGGCCTTTGAGTGTCCTTCTTCTGTTAAACACTTAAAAAATAATTTTTGCTGTAACCATTGACTCCCATAGTATCTGTTTTTCCTAACATGGAAGTCTGTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa29141
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 |
---|---|---|---|---|---|
ENSDART00000093402 | Nonsense | 728 | 1293 | 5 | 14 |
ENSDART00000143222 | Nonsense | 580 | 688 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 5502949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 4962260 |
GRCz11 | 19 | 4878746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGAGGGTTTCCCCATCACCGCCATCAGGGAAATCAAGATCCTGAGG[C/T]AACTCAACCATCGCAGCGTGGTCAACATGAAAGAGATCGTCACTGACAAA
Long Flanking Sequence:
AACATGGTACATTAACTACATAACAAGAAAGAAGCATTTAATGGGGTAGAAAATGCACATATTTGCTCACCAGGGTTTGAAGGGAATTGGCAATTTCTCCTCAACGTTTTTTTAAACTTTCTGTATGAAACTTCAAACAGACCCGGGTGCTCCTGTCAAACCTCCACTAGTTTTTCCTCCATTTCTTGGGTCTAAATAAACCGAAAATAAGCGCTTTCAGCAGTTTCAGCTTAGGGACAAGTGCGTTTAGAATTTTCGCTTTTAGTTGAACTTTTGTTTTGGTGCATCCCAACTTATCATGACTCTCACTAATCACGCTATTCTATATCTGAGGCAGCTAACTTTGGTATAGTGTTTACAAAAAAAAAGACAACATGCTCACAACCTCCTTTTTTGTTTTGGTCTTTAAAGGAGAGCTGGTGGCATTGAAAAAAGTGCGACTGGATAACGAAAAAGAGGGTTTCCCCATCACCGCCATCAGGGAAATCAAGATCCTGAGG[C/T]AACTCAACCATCGCAGCGTGGTCAACATGAAAGAGATCGTCACTGACAAACAAGACGCACTGGACTTCAAAAAGGACAAAGGTCTGGCTAAATGCGTTTGCACGCGTGTTTACATTGTACTTTCAGTTTAAATAAGATGTGTTATTTGCCATTATCCTCCTTTTTGAATGTTTTGTTAACACTTAAATTATATTAAGTAACAATAATGCTAACAACAAACCATTAGCTAAGACGATTTGCTCAAACAGCTAATTAGCTGCTTATTAATAGTAATGTAGTAGTTAAGATGCGTAATTTGCAGTTATCGTCCTTTTAGAATTTCTTTCTGTAACTAAATTATTTTGTCACAATTCATGCTAACAAACCATTAGCTAAGACTATTAGCTCAATAAACCGCTTAATAGCTGCTTATTAATAGTAAGATGGTAGTTGAGTAAGATGTGTAATTTGCCATTATTCTCCTTTTCGAGTTTGTTTCGGTGACACTAAATTATTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23419
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 |
---|---|---|---|---|---|
ENSDART00000093402 | Essential Splice Site | 897 | 1293 | 10 | 14 |
ENSDART00000143222 | None | None | 688 | None | 7 |
Genomic Location (Zv9):
Chromosome 19 (position 5509766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 4969077 |
GRCz11 | 19 | 4885563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGGGCTTCAGTTGAAATGCTGTTTGTCTTCTTTTCTCCCCCGATCA[G/A]TCGTTTGTGTGGTAGTCCATGTCCTGCTGCTTGGCCAGATGTAATCCGGC
Long Flanking Sequence:
AGATCATTTAAGCGAGCTACGAAGAACAGACCCCTGTTGTTCATATCGCAAAGAAAACAAAATATGCAGTCCTAATTGATACAGTGTGTGTGTGTGTATAATTGTGAGTTGATGTTCTTTTCCAGTCGACCGTACACTAATAAGGTGATCACACTGTGGTATCGCCCGCCTGAGCTGCTACTGGGGGAGGAAAGATACTCACCTGCTATTGATGTCTGGAGCTGCGGGTGAGACAGAAGTCTGATTGCCATCATCTCATTACATTTACACCCAAAGTGATTTAAAATAGTAATATTTTTTTTTTGTGTGTGTGCTTTTGTTTAAAGGTGTATTTTAGGCGAGCTCTTCACTAAGAAACCAATTTTCCAAGCCAACCAAGAGCTTCTCCAGCTTGAGCTGATTAGGTGTGTTTGGATGTGTGTTTTTGTCAGTCTAATGCTGAAGGATGGAGAAAAGGGCTTCAGTTGAAATGCTGTTTGTCTTCTTTTCTCCCCCGATCA[G/A]TCGTTTGTGTGGTAGTCCATGTCCTGCTGCTTGGCCAGATGTAATCCGGCTGCCGTACTTCAATACCATGAGACCCAAGAAACAGTACAGGCGACGCTTACGAGAGGAGTTCTCTTTGTAAGTTCAACCTGATTCCTAAAACACATCCACTGCGAACATAACAGACTGTTCGGTTAATGATGGAGGTTTCTTTGACGAAAAATACCGTAAATTATATATATTGTGATTTATATTTTACAATATTTGAGTGTGTTTTCAAATGTCATTTTAATCCTGTGATGCAAAACTTTGTGTTGTTACTCCAAACTTAGTGACACGTGAATGTTGATCATTTCAAGAACTATTTCTCATTGTTATTAATGTAGAAAACAGTGCTGATTAATAGCTTTGATTAAACATTTTTCAGGATGCTTTGAATCGTGTCCTGAGCAAACTTCACAAACGCTGCATCCTTAATAGTTTGACACTGCTGTGATTTGGCTTTAAATGCATAAATACTC
Associated Phenotype:
Not determined