Busch Lab

ZMP

zgc:172096

Ensembl ID:
ENSDARG00000074665
ZFIN ID:
ZDB-GENE-080220-44
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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