ZMP
nek7
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase Nek7 [Source:RefSeq peptide;Acc:NP_001003617]
Human Orthologues:
NEK6, NEK7
Human Descriptions:
NIMA (never in mitosis gene a)-related kinase 6 [Source:HGNC Symbol;Acc:7749]
NIMA (never in mitosis gene a)-related kinase 7 [Source:HGNC Symbol;Acc:13386]
NIMA (never in mitosis gene a)-related kinase 7 [Source:HGNC Symbol;Acc:13386]
Mouse Orthologues:
Nek6, Nek7
Mouse Descriptions:
NIMA (never in mitosis gene a)-related expressed kinase 6 Gene [Source:MGI Symbol;Acc:MGI:1891638]
NIMA (never in mitosis gene a)-related expressed kinase 7 Gene [Source:MGI Symbol;Acc:MGI:1890645]
NIMA (never in mitosis gene a)-related expressed kinase 7 Gene [Source:MGI Symbol;Acc:MGI:1890645]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24175 | Nonsense | Available for shipment | Available now |
sa13206 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24175
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 |
---|---|---|---|---|---|
ENSDART00000079536 | Nonsense | 58 | 297 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 24904223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23162952 |
GRCz11 | 22 | 23177732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGAAGTTTATCGAGCTACGTACGTTCTAGACCACACTATAGTTGCTT[T/A]GAAGAAAATACAGGTAAGAAATTCATCCCATAATGTCATTCAGCAAGACT
Long Flanking Sequence:
TGTCACTAACTGGTCCAGCATAAGTCACTTCAGAAATAGGGATGTCACCACTCGCCTGATTCATCTAGACAGTCTACAGCAAAGATTCATATTGCGCTTTGCTTTGTTCAACATGGAGGGTTAATGTTGATTCGTTCCCACACTCTTTCGCCCTGACATATCACCCCAGTGACACCTATCGAGGATGCCCTCAAGAGTTTGCATCCTTCTCTTGGCATACACTGAAAAACAATAACAAGTTTGGCTTGCAGTGGCCGATTTGAGGAGACGTGTTTTTTTTTGTTTTGTTTTGTTTTTTTCATTTTAGGTTCACGTTGAATGAAAAAGCGCAAATGAAAGCTGTCTGATGTGCATTTTGCTTTGTTTTGTTGTTTGTTTTCAGAAAATTGATATGGGCTATAACAGTTTAGCCAACTTTGCCATTGAGAAGAAGATTGGAAGAGGACAGTTCAGCGAAGTTTATCGAGCTACGTACGTTCTAGACCACACTATAGTTGCTT[T/A]GAAGAAAATACAGGTAAGAAATTCATCCCATAATGTCATTCAGCAAGACTACACTTTAAAACAATTATTTTTTACTAATAAAAGCCTAAATGTCTCAAAATTGGCATACACATTAAAAAACTATATTGCTTGTCTTATAATGATCCCGGTCGAGCCCCCATTTGTTCACTCGGAAAGAAGATATTTTTGTTTCAGGGAATTCTTGGTCTGCCTTTACAGGTTATCATAACTAACTAAAATTTGAATTATTTATATTATATTTAAATTTTATGATACTTAACCAACATTAAAATGAGCCATTTGTTTTACATCATTTGGTAACCTTTGATGTTAGTAAGAAACTGTTGATGTTAGTTCATGGTCTATTATTTAAAGACTGCCCAAACCGATACAATTGTTGATCTTAACAGTGTTTCTAAAATTTGATATTCACATTTAAGGTTTAGAAATCCTGAAGTACCATTATTATTACTTTATATTAAACAATTTATTCAACTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13206
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 |
---|---|---|---|---|---|
ENSDART00000079536 | Nonsense | 283 | 297 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 24833075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23091804 |
GRCz11 | 22 | 23106584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAGATATGTGCATCAACCCGGACCCGGAGAAAAGGCCCGACATCACCTR[T/A]GTGTACAGCATGGCCAAACACATGCACGGTCGGATCGCAAACTGAGTCTC
Long Flanking Sequence:
ATTTGATTTCAGTTTGCTTTTTTTGTACCTCAGCAATAAAACTAACAAATTAAAGCTGCAAGCAGCAATGAAAGGGACCTCATACTAACAAAAAACGTTGCATCAAATTAGAAATGTCGAGCTCTGTGTTAAAGCCATTATTAAAGCCATTATCCATCATTCTCACCATCCTTTAAGGATAAATCTGAACTTTACTAGAAATATGTTAAGCCCCTACGACACAATCTACATTGTGAAAAGCGCTAAATGAAATAAACATGAATAAATAAACATGAATAAGGTGGATGGTGGGCCAAATCAAAGGTTACAATGGGCCAACCAGCTCGCACGCCCTACTTTGGCTTATCCCTTGTTCTGTTTGTGTAGTGTTCTGTATTTTTGATCTGTCTTCTGAATTAACGTGTTGTCTTTTTGTTTGTTTGTTTGTTTGTTTTATAGCTGAGAAAGCTGGTAGATATGTGCATCAACCCGGACCCGGAGAAAAGGCCCGACATCACCTA[T/A]GTGTACAGCATGGCCAAACACATGCACGGTCGGATCGCAAACTGAGTCTCACACCCGATTCCTCTTCCTTCTCCTTTGGCAGAACATCGTTTTGCCTACAAATGTCATTTTAAAGCCTGCAACCTGGCTTCTTTCATTACAAAGTATACAACGTAGGGCACAAAGCAAGGCCTTTGGTTTACTAGAATACATCAAATATAGCAGTCTATAAAGAAGAAAAAGGAAAAACTAAGCAGTGTTGTTAACTGGTTTGACTTGATCTTTGCTCTTTTCAATTTTGGTACAATGCGATTATCGCTTATATACCTCCATTTTTGTTTGTCATCGCATCGGCGGGAAATATTAATATGATACGCTTTCGACAATCTCGTAATCATGAGAAAAACATGACTATCAAAATTACTTAAAATTCTCCCTTAGAAGGCATCTATCTAGCATTCAATATTTGCGAGTGTTTGTCGTTCTATTAAAAGAGCGTGAGGTCATGGTGGCGATTGTCT
Associated Phenotype:
Not determined