ZMP
nek4
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase Nek4 [Source:RefSeq peptide;Acc:NP_957306]
Human Orthologue:
NEK4
Human Description:
NIMA (never in mitosis gene a)-related kinase 4 [Source:HGNC Symbol;Acc:11399]
Mouse Orthologue:
Nek4
Mouse Description:
NIMA (never in mitosis gene a)-related expressed kinase 4 Gene [Source:MGI Symbol;Acc:MGI:1344404]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6189 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8401 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21837 | Nonsense | Available for shipment | Available now |
sa31813 | Essential Splice Site | Available for shipment | Available now |
sa27717 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6189
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058728 | Essential Splice Site | 118 | 849 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 4083263)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 4001767 |
GRCz11 | 11 | 4021154 |
KASP Assay ID:
554-4822.1 (used for ordering genotyping assays)
KASP Sequence:
TGAGAGACAGGTGGTGGAGTGGTTTGTTCAGATCGCCATGGCTCTTCAGG[T/C]AAGTTAATAGMCATTCTTCTCACTAGGGGTGTAAAAATACATCAATATTA
Long Flanking Sequence:
ATTGCAATTATGTTTTATGGCTTAATAATCAAGATCATTTGATTAAATAAACATTAGTCCTTTGATTTCTTTATTTTTTTTTATTTTGATATTTGTCACAAAGCAGGATCATGTAATTTTACTGCAAAATAAAATATGAAAAATGTAGATTGTATAATGTTTTTGAAAATGAGAAAGACATTTTGTTCCAGAATTCAAGACTTGTGCATAATATCTGCTGTGGTTTTTTCAGTATGTGATCAAGAAGCTGAACCTGAGGACGTCCTCCAGACGTGAACGGCGAGCAGCGGAGCAGGAGGCGCAGCTCCTTTCCCAGCTTAAACATCCCAACATCGTCATGTACCGGGAATCATGGGAAGGCGAGGACTGTCAGCTGTACATCGTGATGGGCTTCTGTGAGGGAGGAGATCTGTACCACAGACTCAAACAGCAGAAAGGAGAGCTGCTGCCTGAGAGACAGGTGGTGGAGTGGTTTGTTCAGATCGCCATGGCTCTTCAGG[T/C]AAGTTAATAGCCATTCTTCTCACTAGGGGTGTAAAAATACATCAATATTAGGGGTGGAGTCGCCACAATACAATATAATCACAGTACAAAATTATTGTCACTTTAAATATATTGCTATATTTTGATATTTAATGCAATTTACAACTCTAAATTATGTTGCCAAATGAAAACTTTGGCAACATCTGTTTTAAAGGTGCTGTATGTATTTATTGAACTCCTCTAAAGCATAAAAATACCAGAATATGTTTGCAGATGTTTAAGAAACATGATAAGTAAATATACTTGTATATCAGAAAAACAATGCTAAGTCAGTGAAATGTGTGTTCCATGTCAGAACGTCTGTCATTGTTTTGGTCCTTAACTCCACCCCTGCTGGTTTACCCAATTATATTTTGGCAGCCCGGGTTGCTAAAAGGCTACATGAGGTGGTTTCTAAATGAGCTAAAAAAAAATAAGCATTAGCTATGCAACTTGTGAAGCTCAATTGCCAGGCATGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8401
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 |
---|---|---|---|---|---|
ENSDART00000058728 | Essential Splice Site | 221 | 849 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 4076882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3995386 |
GRCz11 | 11 | 4014773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WACCTCCTCGCATTATACTAACATCATTGATTATTTACTTTCAATATTCA[G/A]TTACCACAGATGCCRAGTAAGTACGACCCTCAGCTRGGAGAACTGATAAA
Long Flanking Sequence:
TTTAGGCATTTGTCGGCGATTTCTCAAAACCTGTCGGCGAGCCAAAATCGGGGCTAAAATCACGCAGTCTGAACTAGGCATTACACGTACATAGGCCATATCCGATCTGTGCCACATGGGAGAAAAAAATTGGAATTGAGTCAGTTGAACAGTGCAGTGTAAATGTGGCCTCACTCACCTTTCAATTGTTTAAAATCTGTTTGAGTTTCTATTTTCTGTTTAATACAAAAGAAGTTGGAAAATATTGAAAACCTCTAACCATTGACTACCATAGCATTTGTTTTTTTTTACTATGGAAGTCAATGGTTACAGGTTTCTGACATTCTTCAAAATATCTTTTTTTGCATTCAACAGAAAAAAACATTGGGAATCACTTGACGGTGATTAAATAGTGAATACATTTTCACTTTTTGATTAATCTACAGTCCATTCATATCAGTACTCTCTCCATACCTCCTCGCATTATACTAACATCATTGATTATTTACTTTCAATATTCA[G/A]TTACCACAGATGCCAAGTAAGTACGACCCTCAGCTGGGAGAACTGATAAAGCGCATGCTGTGTAAGAAGCCAGAGGACAGACCAGATGTCAAACACATCCTCCGACAGCCATATATTAAACATCAGATCTCCATGTTCTTGGAGGCCACTAAAGAGTATGTCTGCCTATTTCTAGCCTTAAAATTATATTAAAATCTAAGCACGCATTGATCTGTCCTGTTACTGATTCTGAACAGGAAAACCGCCAAGTCACGGAAAAATGCAGCGAATGGCAAACTGAACAGTGCTGGATCAGATGCGTCTACCAAACCAAATCAGGTAGTTCAGCCACAGTGTCTCAACTCTGAGTCAAAGACCTGCGGAAAAAAGGTTAGAGGAATGCCATCTTGGAAATCTTATGCACGTGTGTTTTAAATCGACATGATTTTAGTTAGGGCTGCATGATCTCAATGATTTTGCTTAACATTTGTACACTGCTAAAAATGCTTTTCTTGTTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21837
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058728 | Nonsense | 277 | 849 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 4076631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3995135 |
GRCz11 | 11 | 4014522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGCATTGATCTGTCCTGTTACTGATTCTGAACAGGAAAACCGCCAAGT[C/A]ACGGAAAAATGCAGCGAATGGCAAACTGAACAGTGCTGGATCAGATGCGT
Long Flanking Sequence:
CCTCTAACCATTGACTACCATAGCATTTGTTTTTTTTTACTATGGAAGTCAATGGTTACAGGTTTCTGACATTCTTCAAAATATCTTTTTTTGCATTCAACAGAAAAAAACATTGGGAATCACTTGACGGTGATTAAATAGTGAATACATTTTCACTTTTTGATTAATCTACAGTCCATTCATATCAGTACTCTCTCCATACCTCCTCGCATTATACTAACATCATTGATTATTTACTTTCAATATTCAGTTACCACAGATGCCAAGTAAGTACGACCCTCAGCTGGGAGAACTGATAAAGCGCATGCTGTGTAAGAAGCCAGAGGACAGACCAGATGTCAAACACATCCTCCGACAGCCATATATTAAACATCAGATCTCCATGTTCTTGGAGGCCACTAAAGAGTATGTCTGCCTATTTCTAGCCTTAAAATTATATTAAAATCTAAGCACGCATTGATCTGTCCTGTTACTGATTCTGAACAGGAAAACCGCCAAGT[C/A]ACGGAAAAATGCAGCGAATGGCAAACTGAACAGTGCTGGATCAGATGCGTCTACCAAACCAAATCAGGTAGTTCAGCCACAGTGTCTCAACTCTGAGTCAAAGACCTGCGGAAAAAAGGTTAGAGGAATGCCATCTTGGAAATCTTATGCACGTGTGTTTTAAATCGACATGATTTTAGTTAGGGCTGCATGATCTCAATGATTTTGCTTAACATTTGTACACTGCTAAAAATGCTTTTCTTGTTTAGATTTTTTGTCTTGTTTCTAGTCTAAATATCTCAAATTTCTTATATCAAGAAGAATTTTCTTGAAAAGCAAAGAAAATTTTTGAGAAATAATATACCAATATTAAGTGAATTTTTCCTTAAAACAAGCTAAATATTCTGCCAATGGGGGTAAGCAAAATAATCTTGTTTTTTCTTTTGACGTAAGATTATTTTGCTTACCCCATTGGCAGAATATTTTGCTTGTTTTAAGAAAAAACACTTAATATTGGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31813
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058728 | Essential Splice Site | 316 | 849 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 4076511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3995015 |
GRCz11 | 11 | 4014402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCAGCCACAGTGTCTCAACTCTGAGTCAAAGACCTGCGGAAAAAAGG[T/C]TAGAGGAATGCCATCTTGGAAATCTTATGCACGTGTGTTTTAAATCGACA
Long Flanking Sequence:
CACTTGACGGTGATTAAATAGTGAATACATTTTCACTTTTTGATTAATCTACAGTCCATTCATATCAGTACTCTCTCCATACCTCCTCGCATTATACTAACATCATTGATTATTTACTTTCAATATTCAGTTACCACAGATGCCAAGTAAGTACGACCCTCAGCTGGGAGAACTGATAAAGCGCATGCTGTGTAAGAAGCCAGAGGACAGACCAGATGTCAAACACATCCTCCGACAGCCATATATTAAACATCAGATCTCCATGTTCTTGGAGGCCACTAAAGAGTATGTCTGCCTATTTCTAGCCTTAAAATTATATTAAAATCTAAGCACGCATTGATCTGTCCTGTTACTGATTCTGAACAGGAAAACCGCCAAGTCACGGAAAAATGCAGCGAATGGCAAACTGAACAGTGCTGGATCAGATGCGTCTACCAAACCAAATCAGGTAGTTCAGCCACAGTGTCTCAACTCTGAGTCAAAGACCTGCGGAAAAAAGG[T/C]TAGAGGAATGCCATCTTGGAAATCTTATGCACGTGTGTTTTAAATCGACATGATTTTAGTTAGGGCTGCATGATCTCAATGATTTTGCTTAACATTTGTACACTGCTAAAAATGCTTTTCTTGTTTAGATTTTTTGTCTTGTTTCTAGTCTAAATATCTCAAATTTCTTATATCAAGAAGAATTTTCTTGAAAAGCAAAGAAAATTTTTGAGAAATAATATACCAATATTAAGTGAATTTTTCCTTAAAACAAGCTAAATATTCTGCCAATGGGGGTAAGCAAAATAATCTTGTTTTTTCTTTTGACGTAAGATTATTTTGCTTACCCCATTGGCAGAATATTTTGCTTGTTTTAAGAAAAAACACTTAATATTGGCATATTATTTCTTAAAACAAGGCAATATGTTGTGCTTGTGTAGAAAATTCTTCTTGATTTAGGAATTTTTAGATATTTGGACTAGAAACAAGGCAAAAAAATCTAAGTAAGAAAAGCATTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27717
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 |
---|---|---|---|---|---|
ENSDART00000058728 | Nonsense | 631 | 849 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 4065935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 3984439 |
GRCz11 | 11 | 4003826 |
KASP Assay ID:
2260-3863.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAGCCAGAGAGAGGAGAAGACTGAAGCAGTCGCAGGAGAACTCCACA[C/T]AACAAGGTGTGAGGATTTCTGGGAATTCAATGTTATTTTAATGTAAATGA
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATATAAATATATTTAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATACTTTATTGATTTAGAACCAGAATGTAATCAGTTATTTCTGATATTTCCACTCTTGTGTGTTTTGTGCATGTAGGAGAAAGTGTCCAGACCTCTGCCTCCTCTCCCCGAAGATGGAAACAGTGCACAGAAAGACCAGAGCACACCAGCCAATCTCTCGTCCACTAACAAGAGCACAGACCAGCAGGTCACACACACTACTATCTGGAGAAACAACATATGCACACTTGCAGTAACCTCATATGTCCCATAGTTTTGTTCTTTTGAAATTTTACTGTCAGTAAAGCTTTGTTTGTGGGTTTGTTCATACTAAACACTGTATGACTTCCCTCACAGAATCGTCCACTGTCAGCCAGAGAGAGGAGAAGACTGAAGCAGTCGCAGGAGAACTCCACA[C/T]AACAAGGTGTGAGGATTTCTGGGAATTCAATGTTATTTTAATGTAAATGAACAGTCCTTTGAGTCCAATGCAGAGCAGAACTGGACCAAAATAAAACTGTTAAATTATTATAAAACTAAATCAAGCTGGAAAAACTCCCTCTAGAATTATTAGCCCCCCTCCCCTTATATTTTTCCCCTAATTTCTGTTTAACAGAGAGCAGATTTTTTAAACACATTTCTAAATATAATAGTTTTTATAACTAATTTCTGATAGCTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTTTAAGACACTACTATACAGCTTAAAGTGACATTTAAAGGCTTAACTATGGTTAATTAGAAATGTAAGGGTAATTAGGCAAATCATTGAATAACAGTGGTTTGTTCTGTAGACAATCGGACAACAATATAGCTTAAAGGGGATTATAATATTGACCTTAAAATAGTTTTAAAAAATTAAAACTGCTTGTATTCTAGCCAAAA
Associated Phenotype:
Not determined