ZMP
NEK10
Ensembl ID:
Description:
NIMA (never in mitosis gene a)- related kinase 10 [Source:HGNC Symbol;Acc:18592]
Human Orthologue:
NEK10
Human Description:
NIMA (never in mitosis gene a)- related kinase 10 [Source:HGNC Symbol;Acc:18592]
Mouse Orthologue:
Nek10
Mouse Description:
NIMA (never in mitosis gene a)- related kinase 10 Gene [Source:MGI Symbol;Acc:MGI:2685128]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11151 | Nonsense | Available for shipment | Available now |
sa22955 | Essential Splice Site | Available for shipment | Available now |
sa12878 | Nonsense | Available for shipment | Available now |
sa18477 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11151
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 |
---|---|---|---|---|---|
ENSDART00000029001 | Nonsense | 340 | 1099 | 14 | 40 |
ENSDART00000123061 | Nonsense | 340 | 1150 | 13 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 53669356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 49939017 |
GRCz11 | 16 | 50143337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTTWAAATTGTACTTTAAATTTTGGCAAACTGYTTTTTTTCCAGAGAA[C/T]GAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAAT
Long Flanking Sequence:
TTGCTTTGCTCGGTGCAGTGTGTGCGGGATCAGCTGCGTCAGTGTGATGGTGTGCCGGTTCTGCTCAGTCTCCTGCACTCAGAGCACATCAAGCTGCTGTGGAGCACTGTTTGGGTTCTCGTTCAGCTCTGTCAGGATCCCGACACCAGCGCTGAGGTCCGGGCCTGGGGCGGCGTGCAGCAACTACTGCGCATCTTACATGGGTGGGTCATGCTAATTTTGATATTACATGTTCTTTTTCACTTTTAGCATCTTTTGCTGCATAATAGGGGTTTAGGGGCAGTTCTAGGGGCAGTGGAAGTCTATGGGGCAAAAAGTGCAGTGCGACCGCAGAGGTTTTAAAAAAACTATTTGCTACAATCTATTTTTTCCTACACACATATAAATATTATATTGCATCATTTTGATTAACATTTTAATACTATTTTAATGTTTAAACAGCATTTTAGGTCCTTTAAATTGTACTTTAAATTTTGGCAAACTGTTTTTTTTCCAGAGAA[C/T]GAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAATGCAGCAGGCAGAATCCACAGTCAGCAGGTGTCAGCAGTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGGTGAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACACTGCAAGTGTGAGCAGAGCGTGAGCAGCGCGTGTTTTTCGCCGTCCATGTTAACAGATTAGAGCTTTCATACTGCATGCAGAAGCAGCATGTCAGCACGAGAAGTAGTTTGGGCAATGGGTCTATTTTGGCCACGTTGCTCACACTCAATTAAAGTGACAGTGCATTGATATGGACCAAAACACATTGAATGACAAAAAAAGTATTTAAAAAGACAATTAAAAAGTAGAGATTTTACCCTATAAATGCATCAATAAGATCCACAGATTTTTATATATTCAATCAAATGAACTTAAACGATTAAAATAAAATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22955
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 |
---|---|---|---|---|---|
ENSDART00000029001 | Essential Splice Site | 385 | 1099 | 14 | 40 |
ENSDART00000123061 | Essential Splice Site | 385 | 1150 | 13 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 53669219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 49938880 |
GRCz11 | 16 | 50143200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGG[T/C]GAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACAC
Long Flanking Sequence:
TCCCGACACCAGCGCTGAGGTCCGGGCCTGGGGCGGCGTGCAGCAACTACTGCGCATCTTACATGGGTGGGTCATGCTAATTTTGATATTACATGTTCTTTTTCACTTTTAGCATCTTTTGCTGCATAATAGGGGTTTAGGGGCAGTTCTAGGGGCAGTGGAAGTCTATGGGGCAAAAAGTGCAGTGCGACCGCAGAGGTTTTAAAAAAACTATTTGCTACAATCTATTTTTTCCTACACACATATAAATATTATATTGCATCATTTTGATTAACATTTTAATACTATTTTAATGTTTAAACAGCATTTTAGGTCCTTTAAATTGTACTTTAAATTTTGGCAAACTGTTTTTTTTCCAGAGAACGAGTGTATGTGTCCGATCGCTCCACCATTGATTCAATTTCCAGCGCCAATGCAGCAGGCAGAATCCACAGTCAGCAGGTGTCAGCAGTGGTGTGCGCTCATGAAACAGCGGAGAACACCATCAGTCTGCAGTCAGG[T/C]GAGGAGACTCAGAAAATGTAGGAATTATGAACCTAAAGCCTGTTTTACACTGCAAGTGTGAGCAGAGCGTGAGCAGCGCGTGTTTTTCGCCGTCCATGTTAACAGATTAGAGCTTTCATACTGCATGCAGAAGCAGCATGTCAGCACGAGAAGTAGTTTGGGCAATGGGTCTATTTTGGCCACGTTGCTCACACTCAATTAAAGTGACAGTGCATTGATATGGACCAAAACACATTGAATGACAAAAAAAGTATTTAAAAAGACAATTAAAAAGTAGAGATTTTACCCTATAAATGCATCAATAAGATCCACAGATTTTTATATATTCAATCAAATGAACTTAAACGATTAAAATAAAATATTAAAATTAAAATTGATTAAAATTAAATATTTATTTGGACCCGAACTACAAAACCAAATTTAACACAATTAGTATTAGTTTTGCTTAAGTTGCACACTAGTTTGATCATGTTTAAATATCATTATAACTATATTGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12878
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 |
---|---|---|---|---|---|
ENSDART00000029001 | Nonsense | 516 | 1099 | 19 | 40 |
ENSDART00000123061 | Nonsense | 516 | 1150 | 18 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 53665809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 49935470 |
GRCz11 | 16 | 50139790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTAAACCAGAACCGTCCTCCTATAAGAGTGGTCAATGGTTATGCGGTTT[T/A]GGAGCATCTAGGMAGCGGAGCTTTTGGCAGCGTCTTTAAGGTCAAGATGA
Long Flanking Sequence:
TATTATTTCTATATTTAATTAAAATATTTTTACTTTTTTGTTTCTTTAATTTTATTTAAAGATAATATATGAATTTTATTTCTTTTTTAAGATTTCTTTTTTTTTGCTTTTTTTCTGCATGATATAGTTGTTGTTTTTTTATTTTTTTATTCATCGATATCGTTACTTTTATGAAACCATTTTTTAACATTTATTGGTTCTAAATGGTTTGTTTGTTTCCAGGCTGTTTTCTCCAGATTTGTTTGAGATGTTTATCGATGTCGGTCACTACGTTCGAGACATTACTGCATATGAACCGCTGCAACAGAAAATCATGCTTTTATCTGTAAGATCCTGAAGTTATTACACTCATAAAATACACTGGAATATTTTCTCTCTTGCATATTTACATTATGACTGTGTTTATCTGCAGCCAGAAGAGTTGGATATTCTTAGGGAAAGCATCGAGACAGTAAACCAGAACCGTCCTCCTATAAGAGTGGTCAATGGTTATGCGGTTT[T/A]GGAGCATCTAGGAAGCGGAGCTTTTGGCAGCGTCTTTAAGGTCAAGATGACCTGTGCTGGTTATTGTTGGTTAATAGTTAAATCAAGCCATTCACGGTTGTTTTTTGCGCCCACTCATAGGTTCGTAAGCAGAACGGACAGAACATTCTGGCACTTAAAGAGGTCAACTTTCACAATCCGGCCTTTGGCAAAGATAAGCGATCCAGAGACAGCAGTGTTGAGAAGATTGTGTCTGAAATGACCATCATTAAAGAACAGGTTAATCTCATTCATAAACAGCTCCAACATTTCATTCCACTTCATTTAGGTCAGACGTCCACCTAGTGCTCTATTTTAACGATCTAAGCACAGAGTCTAAAGCTCATGGTGCAATTGCACCAAGATTCTGTCTGAGTCCACTTTTGCTATTTTAAGGTCGGGAAAAACATCTGTTCACAAGGCGCATGGTCTAAAAAGGTTTATCTTTATTCTCTTTTGGCATAACCTGCATTAAACTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18477
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029001 | Essential Splice Site | 759 | 1099 | 26 | 40 |
ENSDART00000123061 | Essential Splice Site | 759 | 1150 | 25 | 41 |
Genomic Location (Zv9):
Chromosome 16 (position 53652874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 49922535 |
GRCz11 | 16 | 50126855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTAGAAGACAAAACCTTCKCCGAAAGAGTAACCGACATGATTAAATGG[T/A]AGGATTCCCTGAAAACTGCTTTCNNNNNNNAGATATAAACACATGCAGCC
Long Flanking Sequence:
CTCAGTTTTAATATGAAATGTTGCATGTATTGAAAAACAATAACACAAATAAATACATAAATAAATAAATAAATAAATATGTGAATGTAAAAAATAGCTTAAATTTTTTTAGCATAGTATCAATAATATTTCTATATCAAATAAAACTATATATATATATATAGTTTTTTCAATTTTTTTCAATCATTTTTATATATATATATATATATATATATAAATCAAAATTATGATTGAAAAAAATTATTTTAGATTTAAAAAAATAACATTTCAAGGCTTCTTTCATTTTTTTTACGTTAAATAAGCCAAGTGAGACCCCTTTCTTTAAATGATGCTTTTTAATTACATTTTTACCAGACATTTTTACTCACATGTTTCAAATGTTTGTCAGATTTGATTATTCTGAATTTTAATGTCGTTCATGTGTTTAGATTGTGGAAGCTGTTTATGAGCCACTAGAAGACAAAACCTTCTCCGAAAGAGTAACCGACATGATTAAATGG[T/A]AGGATTCCCTGAAAACTGCTTTCTGCTTTCAGATATAAACACATGCAGCCTGGATACAGATATGAGATTGTTGTAGAAATGTAAAATCTTGAAAATGACACACAATTTCATATGTTTTTTTTATTTATTTTATTTTAATTAAATGAAGAGAAATTATGATCTGAAAGTGATGCAACAGATGTATTATTTTACCAGCATTGTTATTATTATTCTTATTATAAGAAAAGCCTTTGTGTTATAAATTATATTTAAAGAAAAATGTGTATCAAATGTCCTTTGTGCTGCCAGCCATTGGAATTTAAATACTGAGTTTTAAGTATGAATAGGGTTTAATTAAGTTTTTGATTTATGTGATAACATTGAATGTATTTGTGTTGCCTGTTTTCTGTGAAATGTGTGATGTGAACGCTGCTGTGGTTGTGTGGTGAAGCCAAAAATAAATTTAAAGTAAAGTAAAAAATATTTATAATTCTATTCTTCATCCCAAGTACAACTAATGC
Associated Phenotype:
Not determined