ZMP
zgc:172096
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC572146 [Source:RefSeq peptide;Acc:NP_001121732]
Human Orthologue:
CDK14
Human Description:
cyclin-dependent kinase 14 [Source:HGNC Symbol;Acc:8883]
Mouse Orthologue:
Cdk14
Mouse Description:
cyclin-dependent kinase 14 Gene [Source:MGI Symbol;Acc:MGI:894318]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1175 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
sa2845 | Essential Splice Site | F2 line generated | Not yet available |
sa18680 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1175
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000034421 | Essential Splice Site | 77 | 310 | 2 | 10 |
ENSDART00000100602 | Essential Splice Site | 77 | 324 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 57603519)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54196939 |
GRCz11 | 16 | 54078431 |
KASP Assay ID:
554-1085.1 (used for ordering genotyping assays)
KASP Sequence:
CGTCTGGCAAAGAGTCTCCCAAACTGCGCAGACACTCCAGCCCCAGCTCT[G/A]TGAGTCTCTCAACAACATTATACTACAGGCTAAAGAATTCCGCATTCTGA
Long Flanking Sequence:
AAGGCTATTAAACTGATTATATTTTAATTACATTACAACATTGATGCTGTAAAAGGAAGCTCATGAAGTTGAAAACAGTCATATTTACCCCTCACCAGAAGTTTATTAGTGGGGAAAACCTCTAGCTGTACATATACCCTATTATTATTATTATTATTATTATTATGATTATTATTATTATTATTATTATGATTATTATTATTATTATTATTGCAGTCCTGACGTATTGTGTGTGTGTGTATGTGTTTGTGCAGATATGTGTCACCAAGATGTCCACTCGCAGCTGCCAGGGATCAGACTCGGTCATCAAGCCCCTGGACACCATCCCTGAAGACAAGAAGGTGCGCGTGCAGCGAACGCAGAGCGGCTTCGAGGCCTTCGACAAACCTGCCAGTCAAGTGAAGCGCGTTCACTCCGAGAATAATGCCTGCATCAACGCCAAGAGCTCCTCGTCTGGCAAAGAGTCTCCCAAACTGCGCAGACACTCCAGCCCCAGCTCT[G/A]TGAGTCTCTCAACAACATTATACTACAGGCTAAAGAATTCCGCATTCTGATTGGCTGATGAGTGTTCTCAGGTGTTTGGTTATTATCAGATAAAGGCACAGCTAAAGTAGTTCCGGCAGGTTTTGAGTGCATTACAGCTCTATATCATTCCGCTGAATGATTAGAGTTATTTCACAGATACAACAGTCAGAAATCACATGGGAACACAACAGAAGGAGGATGAGGAGATGTGGAGGACACTAGACCTGTATGTTGAGTTATGATAAAATAATGCACACCTGAGGTGAAACTGTCACTCCTCTTCACCACATCTTCACCTCAGGCATTTTATATTTTTTAATAATTAATGGTACTGTTGTTAGTTCTTATGCTACGGGGCTTTGTTGAATGTTTGATTCTGATTGGCTGATGAGCATTCTGAGGTGTGCTGTTATTATCAGATAAACGAACAGCTAAAATAGTCATCAAACACAACACTTTAACAGTGTCTTTAGGTGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2845
Status:
F2 line generated
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034421 | Essential Splice Site | 189 | 310 | 7 | 10 |
ENSDART00000100602 | Essential Splice Site | 189 | 324 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 57565016)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54158436 |
GRCz11 | 16 | 54039928 |
KASP Assay ID:
554-2684.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTCAATATGATTTGTGATGCTCACAGWGAACTCTTCTGTTGTTTCCGC[A/T]GTTGTTCCTCTTCCAGTTATTGAGGGGTTTGTCGTATATTCATCAGCGCT
Long Flanking Sequence:
TTAAAGGCTTCACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTATGGAGACAATCCAAAACTAATATAGCTTAAGGGGGCTAATAATATTGAGCTTAAAATGGCTTTAAAACAATTAAGAATTATTTTATTCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAATATTAGAGGAAATATGTAGAAAAATTTCTGAATCTGTTCAACATCATTTAGGAAATATTTTTGAAAAAAAGAAAGTCACAGGATTGCCAAATAATTCTGACTTTAACTGTAAATGCAAGCAATCTTTGTTGAAGTTACAAATACTATATTTTCATGTACTCATGCTTTAAACTCTCTTCCATAGCAGCTCTAGTGTGAAACCTGCAGCTCTGTGTTGTAGGTTATGTCGTGATTGTGTGTGTATGTTGTGTCAATATGATTTGTGATGCTCACAGTGAACTCTTCTGTTGTTTCCGC[A/T]GTTGTTCCTCTTCCAGTTATTGAGGGGTTTGTCGTATATTCATCAGCGCTACATCCTTCACCGAGACCTGAAGCCACAGAACCTGCTGATCAGCGACACCGGAGAGCTCAAGCTGGCAGACTTCGGTGAGTCTTCTTCACTAATAAATAGCTGGATTATTGCACATTTTTAATTGAATACATTTAATTTCTACATTTAAAAAAAGATGTATTAAATATGGCAAATATTCACATTTTAGATGTTATTTAATCATGATTATATTAATTTAGCATTTTTCATTATTTTCACATTGAAGACAGATGTTACATAATAATAGTAAATTATCATATTTAATGATTTATTATGGGCGTCACGGTGGCGCAGTGGGTAACACAATCGCCTCACAGCAAGAAGGTTGCTTGTTTGAGCCTTGGTTGGGTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCGGATGCTCCAGTTTCCCCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18680
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 |
---|---|---|---|---|---|
ENSDART00000034421 | Nonsense | 251 | 310 | 8 | 10 |
ENSDART00000100602 | Nonsense | 251 | 324 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 57549458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 54142878 |
GRCz11 | 16 | 54024370 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTCCGTCCCCAGCCACACRTACTCTAATGAGGTGGTGACGCTGTGGTA[T/A]CGTCCTCCAGATGTGCTGCTCGGCTCKACAGACTACTCCACCTGTCWGGA
Long Flanking Sequence:
TTTTTTTTTAAAATATTTCCTAAATGATGTTGAACAGATTCAGGAACTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTTTATAGTTTTAAGGCCATTTTAAGGTTAATATTATTAGCTCCCTTAAGCTATATTTGTTTTGCATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTACTTACCCTAGTGAAGCCTTTACATGTCACTTTAGGCTGAATACTAGTGTCTTGAAGAATATCTAGTCTAATATTATGTGCTGAACAAAAATCTACAGCAGGGCTTCAACTGTATATAAGCACACTCTTAAAATGCTGGGTCGTCTTCTTAAAGAGTGATGCTGATGTGTGTGTTTTGTGTGCAGGTCTGGCAAGAGCAAAGTCCGTCCCCAGCCACACATACTCTAATGAGGTGGTGACGCTGTGGTA[T/A]CGTCCTCCAGATGTGCTGCTCGGCTCTACAGACTACTCCACCTGTCTGGACATGTGGTGAGACACCTATCAGACATCTATATATGTCCCTATTCCGGTCCTAAGACTTCTTATTACACACACAGGGATGTACAGCAGTACACAAATATCTTTAAATCTGAAAAATTAAAAGATTAACATGTAAAGCTATGTATTATTGTCTACATAAATATAAAAACTGCTCCTCCTTTCATCCCTTCTTCACATTGGGGGGCTTTGGTGGAATCCGGCTCCATTGTTGTTGAATTATTAATGAAAATTTAAATTTGTCGATCGATCAGAAAACATACTCCTAGCAATATGCCTAATGGAAATGCTTTTGCTAGTTTGTAGCCGATAGCCGATGTGTTTGTATTTGCGTGCATGGTTTTGTGCATGCATGCGTGTGGTCACAATTGAGTGTGTGTGTGTGTGCTGGACCAGCTCGTCTTAGTTCAGCAGACCTTTCACACTGCTGCAGAT
Associated Phenotype:
Not determined