ZMP
pkn3
Ensembl ID:
ZFIN ID:
Human Orthologues:
PKN1, PKN2, PKN3
Human Descriptions:
protein kinase N1 [Source:HGNC Symbol;Acc:9405]
protein kinase N2 [Source:HGNC Symbol;Acc:9406]
protein kinase N3 [Source:HGNC Symbol;Acc:17999]
protein kinase N2 [Source:HGNC Symbol;Acc:9406]
protein kinase N3 [Source:HGNC Symbol;Acc:17999]
Mouse Orthologues:
Pkn1, Pkn2, Pkn3
Mouse Descriptions:
protein kinase N1 Gene [Source:MGI Symbol;Acc:MGI:108022]
protein kinase N2 Gene [Source:MGI Symbol;Acc:MGI:109211]
protein kinase N3 Gene [Source:MGI Symbol;Acc:MGI:2388285]
protein kinase N2 Gene [Source:MGI Symbol;Acc:MGI:109211]
protein kinase N3 Gene [Source:MGI Symbol;Acc:MGI:2388285]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17281 | Essential Splice Site | Available for shipment | Available now |
sa44608 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17281
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112546 | Essential Splice Site | 318 | 940 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 33481032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31243264 |
GRCz11 | 5 | 31843417 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TSTTGTGTATGGCTGTTGGATTGTGWATAATTGTGYRTGCATTTGTTTTC[A/T]GGGCGATTGGAGGTCAGGTTGATGGGTTGTCAGGACCTGCTGGAGTCAGT
Long Flanking Sequence:
TTGCCATATCAGTTATTGACCAGAGGGGACTGATCCAAATCCTATACTGCTCGCATACTATTCTGTGATATTGTTAAGCCCCATAAAACCCATCAAGCTATTATAAGGCATCATTGCATTTTTATTCACTAAATTACAAATGTTGTACAAAGCCATTTTTAGTGTGAGATACAGATGATTATTCAAGTTCACATCAGCACAAATTATGATTTGGTTTTTCATTAGCTGTTGTTTTTTTAGTAGGTGTAGTTGATTATATTTAATACACGTGATGTATTATTATTAGTTATATATTTTTTTCAGCCCAGATTATCAGAAGTATTGAAATTGTTGTATCGGAAAGGTATCTGCATCAGCCGCATTTTTGTATATTTTAATACAGTGGTGATGAATAAATGTAACTAATCTGTGTGTGATGTTTGTGCATGTTGTTTTGTTAACGCGTTTTTGTGTTGTGTATGGCTGTTGGATTGTGTATAATTGTGCGTGCATTTGTTTTC[A/T]GGGCGATTGGAGGTCAGGTTGATGGGTTGTCAGGACCTGCTGGAGTCAGTTCCAGGCCGCTGTCGTGTAAGCAACATGTCCTCCGCTCCTGGAAGTCCATCTGACTCCAAATCACTAAGAATGAGAACCGGCCTTTCCACTCGCAGCACCAACGGCAAGACCACCAAGACTGATGAACTGTCATGTGAGTTTCTCACGGGCAGCAGGGTGAAAAATAATAGATTTCATAATAATAGTTAAAAAAAAAAACTGTTGAAAACTTTTATTTTGTTGTCCAAATACATTTTTAAAATGGATAAAACAAATGTTACTGCAGTAATTATTATAAAGCCATTCAATTTATCTTTTTTTTATTCACATGCACTTTTTTTTTTTCTAATCAAAATAACTAGGGGTGTAACCGATCACAGTTGATCTGTGATTCGTACAGAACACAACCCACAGTTTGGAACACAAGTGGCCCTCGGATTAATACTTTTTTTTTTTTTTTTACTTCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44608
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 |
---|---|---|---|---|---|
ENSDART00000112546 | Nonsense | 319 | 940 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 33481028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 31243260 |
GRCz11 | 5 | 31843413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTATGGCTGTTGGATTGTGTATAATTGTGCGTGCATTTGTTTTCAGGG[C/T]GATTGGAGGTCAGGTTGATGGGTTGTCAGGACCTGCTGGAGTCAGTTCCA
Long Flanking Sequence:
CATATCAGTTATTGACCAGAGGGGACTGATCCAAATCCTATACTGCTCGCATACTATTCTGTGATATTGTTAAGCCCCATAAAACCCATCAAGCTATTATAAGGCATCATTGCATTTTTATTCACTAAATTACAAATGTTGTACAAAGCCATTTTTAGTGTGAGATACAGATGATTATTCAAGTTCACATCAGCACAAATTATGATTTGGTTTTTCATTAGCTGTTGTTTTTTTAGTAGGTGTAGTTGATTATATTTAATACACGTGATGTATTATTATTAGTTATATATTTTTTTCAGCCCAGATTATCAGAAGTATTGAAATTGTTGTATCGGAAAGGTATCTGCATCAGCCGCATTTTTGTATATTTTAATACAGTGGTGATGAATAAATGTAACTAATCTGTGTGTGATGTTTGTGCATGTTGTTTTGTTAACGCGTTTTTGTGTTGTGTATGGCTGTTGGATTGTGTATAATTGTGCGTGCATTTGTTTTCAGGG[C/T]GATTGGAGGTCAGGTTGATGGGTTGTCAGGACCTGCTGGAGTCAGTTCCAGGCCGCTGTCGTGTAAGCAACATGTCCTCCGCTCCTGGAAGTCCATCTGACTCCAAATCACTAAGAATGAGAACCGGCCTTTCCACTCGCAGCACCAACGGCAAGACCACCAAGACTGATGAACTGTCATGTGAGTTTCTCACGGGCAGCAGGGTGAAAAATAATAGATTTCATAATAATAGTTAAAAAAAAAAACTGTTGAAAACTTTTATTTTGTTGTCCAAATACATTTTTAAAATGGATAAAACAAATGTTACTGCAGTAATTATTATAAAGCCATTCAATTTATCTTTTTTTTATTCACATGCACTTTTTTTTTTTCTAATCAAAATAACTAGGGGTGTAACCGATCACAGTTGATCTGTGATTCGTACAGAACACAACCCACAGTTTGGAACACAAGTGGCCCTCGGATTAATACTTTTTTTTTTTTTTTTACTTCAATTTAGA
Associated Phenotype:
Not determined