ZMP
zgc:153916
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC567134 [Source:RefSeq peptide;Acc:NP_001073501]
Human Orthologue:
PKN2
Human Description:
protein kinase N2 [Source:HGNC Symbol;Acc:9406]
Mouse Orthologue:
Pkn2
Mouse Description:
protein kinase N2 Gene [Source:MGI Symbol;Acc:MGI:109211]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45871 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44371 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32553 | Nonsense | Available for shipment | Available now |
sa38152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19376 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24742 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45871
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 |
---|---|---|---|---|---|
ENSDART00000113923 | Essential Splice Site | 252 | 977 | 5 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 122214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25351496 |
GRCz11 | 6 | 25342057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCTATTGGGAACAGGAAAGGTGACAGAGAAGAAAGCTCATTCTGAG[G/A]TCAGTCTAAATCCTCATAGTTTTTATATAGTGTTCTCTGCATATGCTTTC
Long Flanking Sequence:
TATGAAAAATAATAATTTAAAGGCTGATAGCTTTTCATTTGCATGTTTTTGCTTTTTACTTTTAAAATCTACAATGTTTTTCTTCTGTAAGTTATGGTTCAAATAATAATTATTGGGTAATTTTTATAGTTGTAATAAAATTTATTTGACTTTTTAAATCACCAAGCAAACAACTGATTTAGCCTGTAAAGTGTAGACCGAGATAATTTTTCTGAAACACCATAAAAACAGTCTGCACAAGGAGCGTTTTTATTATAAAACACAGTTTAAAAATGCACTAGTGTGAACGGCTCCTCAGTTGCGGTTTAACATTTTGATGTTAAAGCAAAAATCTTATGTTGGCAGTGACTACAAGCAAGCCCATCATCAGCCCTCTGGACCTGAGGATAGAGGAGCTGCGACATCACTACCGGATAGAGTCTGCTGTGGCCGATGGTGCCAAAAATGTGATGAAGCTATTGGGAACAGGAAAGGTGACAGAGAAGAAAGCTCATTCTGAG[G/A]TCAGTCTAAATCCTCATAGTTTTTATATAGTGTTCTCTGCATATGCTTTCATGCCTGTATAGCTGTTTAATCCAGTTACTCATTTAACTGTTTGCTTGTAACAGCTTTTGTTGCCTGAAGCAGCAGATGTTTACAGCTTTTCTCATTGTGTATCATATTAATTGTGCTATGACACAGAATGCTTAAATGTTCTTTCTTATGTAATTGTTTTATAATTGTGAGAGTAATACAGTTTTTTATACAGCGGTTTATATTAAAATGTGTTTAAATTATTTAGTTTTGGGATGCAACAGTGAAAATATCTGTCCTACGTGACAGAAACCTTTTTTTTTTTTTTTTGTTGGTTAGAAAATCTATATACAGGGTGAAAATGCTGGCAACACATGATAGCAGTAAATTAGACAGCTGCTGAATCACTGCATATTTGGGTTTGTTCCTATTGCACAACTGGTAGAACAAGGAAAAAAAAAAGTCTTGTTTGATTTTGTGGGATAGAGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44371
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 |
---|---|---|---|---|---|
ENSDART00000113923 | Nonsense | 401 | 977 | 8 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 113408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25342690 |
GRCz11 | 6 | 25333251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCAGATGAAATCAGTGCCGTTCTAAAGTTGGACAACACAGTTGTGGGA[C/T]AGACCCATTGGAAGCCAGTTAGCAACCAATCTTGGGACCAGAAGTTCACG
Long Flanking Sequence:
TTTCATTGACATTAGAAAAGATTATTAATCATTGTAATAAATGTATTATGTTTTGTTCATTGTTTGTCTTAGTAAATAAATTTATTACCATTAATTAATATAACCTTATCGTGAAGTGTTGCCATTAAATTACATTGTTTACCATAAGTTTTCATTATTATTACAGTGTATATTGTAAGTAGTGCTTTCAATTGATTAAAATATTGATTTACTTACCTTTTTAAGTTTAATTCAAATGCTTGATATTTAATTCAAATTTTGTATTGCAGATTTTTATTAACTTAATCATTTAATTGCATATACCAGTATTTGCTTTATACTTAAATTGAAAAGTATTAGATAACAGATTACAAGATTGCAATAAGTAAATGTATTAAGTAATCCCTAATGAATCTATCCCTAATAAATATATCTGTTTTTTATTTCTTTATTTTTTTTTTTGTGCTGGTATGGCAGATGAAATCAGTGCCGTTCTAAAGTTGGACAACACAGTTGTGGGA[C/T]AGACCCATTGGAAGCCAGTTAGCAACCAATCTTGGGACCAGAAGTTCACGCTGGAACTTGACCGGGTAATGCATGAGAAATTTCATAAAGCACACTTGTCAAACCATAGCCTTATCCCATAATCCTCTCCCAACATATGAGTAGATGGGCACACATATGCACACATGCTCTCCATTCCAGCCTCTCTCAATTAACTTTAGAAATGTTAATCCCAGATTTGACCCAGTTCTAATGGAAAGTTTCACAAGGCAGATCAGAAGTCATCTGTAATCTCTGTGCTCATATATGTACAGAACAAAACTTATTATTTTTATTATTTATTTTTATTTTTTTGTCAAGGAAATTGAAAATTACAAAGCAGAATTATATCGAGCAAAATTGGTTCAGTTGACTGTCTGTACATTTAAAAATTTTGTAACTCTTACTAAACCTGAATGCTGATATACAGTGCTGAGAAAATAAAAAGGAATCAGACAACAGGCTAAATATAAATAACAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32553
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113923 | Nonsense | 615 | 977 | 13 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 103439)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25332721 |
GRCz11 | 6 | 25323282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTCGCGACCTTTGACTTCCTGAACAACACAGTAGCAAAACCAGATTA[T/G]GACAGTCTGGTTGAACATGAGCAGCCTGGCTTGGAACTTACTGAAATTCA
Long Flanking Sequence:
TCACTAATGGCCAGGACTTTTCCCTCTGGTGACATGTACAAATGGGGAATATTAATCAATCAAAGGGTTTCTACAGACTGTTTTTATGAAATGTGATTCAAAGAAATAGAAGGGGTTCAATTTTACAATTAAAGGCTGGCTGTGTTCACACACAACTGTTTAAACTCTGAATAAAACAGATTTTTGCATAATAAATCCCCTTTAAATCATGTTTTATTTATTTATTTATTTATTTATATTTATTTATTTTTATCATTTTTGGACCTTGACTGTCCATAACCACCATTCACATTAATTGCAACAAACGCACAACATATTTGAAAGGCAGTAATTAGAGTATGGAAATGATGTCAAATCTTCATTTTTTTGGCTGAACTGTCCCAGTATTTTCAGTAAGAGATCTCTTGCACTGGTTTGGAAAGATTCTTAAGTGCCTCTTGCTTACAGGATGCCCTCGCGACCTTTGACTTCCTGAACAACACAGTAGCAAAACCAGATTA[T/G]GACAGTCTGGTTGAACATGAGCAGCCTGGCTTGGAACTTACTGAAATTCAGCGAAAAACTGAAATAAGGTATTCTCTTTCCCATCACCATGATGATACTGTTAAAACATGCATATAGTAATGCATGTAGTAATACACTGGAATGCATTTGTCGTTTTCAAGTTAAATTGAATAGATTGCACAAGTGATTTGAACCTAAATGGACTTAAATACATACAGTATTATCTTACATCGTGTATCAAATGTTTGTGTGCCTTCAGGGAAGAAGAGGAAGTTCAGTTCAGTTTGTCAGATTTTAAATGTGTAGCTGTTCTGGGACGTGGCCACTTTGGAAAGGTAAACGTCATGTTTTCATCCGTACAAAAGGCAAGCTCTGTACAAGTATGCAAATGCCCCATGCATTTGACCATTTGCATAGATAGAATTTTAGATTATCGCTACATACTGCCAGTTTGCATGAGTCACTTTCATTGTCTCGTAACTATATTTATTTATTCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38152
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 |
---|---|---|---|---|---|
ENSDART00000113923 | Nonsense | 644 | 977 | 14 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 103163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25332445 |
GRCz11 | 6 | 25323006 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACATCGTGTATCAAATGTTTGTGTGCCTTCAGGGAAGAAGAGGAAGTT[C/T]AGTTCAGTTTGTCAGATTTTAAATGTGTAGCTGTTCTGGGACGTGGCCAC
Long Flanking Sequence:
TAACCACCATTCACATTAATTGCAACAAACGCACAACATATTTGAAAGGCAGTAATTAGAGTATGGAAATGATGTCAAATCTTCATTTTTTTGGCTGAACTGTCCCAGTATTTTCAGTAAGAGATCTCTTGCACTGGTTTGGAAAGATTCTTAAGTGCCTCTTGCTTACAGGATGCCCTCGCGACCTTTGACTTCCTGAACAACACAGTAGCAAAACCAGATTATGACAGTCTGGTTGAACATGAGCAGCCTGGCTTGGAACTTACTGAAATTCAGCGAAAAACTGAAATAAGGTATTCTCTTTCCCATCACCATGATGATACTGTTAAAACATGCATATAGTAATGCATGTAGTAATACACTGGAATGCATTTGTCGTTTTCAAGTTAAATTGAATAGATTGCACAAGTGATTTGAACCTAAATGGACTTAAATACATACAGTATTATCTTACATCGTGTATCAAATGTTTGTGTGCCTTCAGGGAAGAAGAGGAAGTT[C/T]AGTTCAGTTTGTCAGATTTTAAATGTGTAGCTGTTCTGGGACGTGGCCACTTTGGAAAGGTAAACGTCATGTTTTCATCCGTACAAAAGGCAAGCTCTGTACAAGTATGCAAATGCCCCATGCATTTGACCATTTGCATAGATAGAATTTTAGATTATCGCTACATACTGCCAGTTTGCATGAGTCACTTTCATTGTCTCGTAACTATATTTATTTATTCAACAGGTTTTACTCGCCGATTACAAAACCACTGGAGAAATGTTTGCCATTAAAGCTTTGAAAAAAGGTGACATCGTTGCAAGGGATGAAGTGGACAGGTAACGGCTCTGCGCTCGTGTTTAAGTGGAATAAATGAGCTGTATCTTATTCTTGAGGATGTTTTGAAGCATTTGTAGAGGCATCAGTAATTGTATACAGCGGGGACTCCTCTGCTACTGTTTTACTTCCTGTTATTATTAAAGACAGAGTCAGAGTTGTACTCTAGACATGCTGGAGCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19376
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113923 | Nonsense | 735 | 977 | 16 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 100371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25329653 |
GRCz11 | 6 | 25320214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTTTCCAGACCAAGGAGCATGTGTGTTTCGTCATGGAGTACGCAGCT[G/T]GAGGAGACCTGATGATGCACATCCATGCAGATGTGTTTTCTGAAACGCGC
Long Flanking Sequence:
TGTCCGTATATCAATGTCAGTGAAGTAATCTCATAGGTTTCTCTGCCTGATAAAGGATACATTTAGCAACAGATATTAATTTCTGTTTTTATTTTTCTATATAATGATCTGCACTTGTATAAATAACGCTCCTATATATTTTTTTAAATTGCAAAGAAATATAGCAAAAATATTTATTTGGTTAACTCTTGTGTATTTGATTAGCAACCATTCTCCTCAATGCTTCTTAATGCTCCTCAATAAGCACAATTCCTTGGTAGAGTTTTACAATCTGACTTAATACATATGCTTAAAAAGACATAAGGTGAAGCACTACTTTTTTGTTCACTCCGATGGATGGACTTGTCAGTTTACACTATCCATTATTGTCTTTCCGCAGCCTGATGTGCGAAAAGAGGATCTTTGAGACTGTGAACAGTGTTCGGCATCCATTCCTGGTGAACCTCTTTGCTTGTTTCCAGACCAAGGAGCATGTGTGTTTCGTCATGGAGTACGCAGCT[G/T]GAGGAGACCTGATGATGCACATCCATGCAGATGTGTTTTCTGAAACGCGCTCTGTGTGAGTAACTCGTATATGTGCTTTTGTACTGCTGCTGCTACTGTCATGTTCACACAACTGGTTGTGTTTAAGCTGGCACATGAAACCCCATGTTTTGATAACATCTGACACAGATCAGCATTTGTTACACATGTGTAAGCAAAAACGATTTATCTATTTATCTGTGTCAAATACTTTAAAGTTTTCAGTTTAGTTTCAGTTTCCTTTATTTTTGTCATTAAAAACATCACAATAAATTCCAATGCAGAACAAAATTATATTACATCGGACCCAGCAAGAACATAAAAAAACATCAATCACTAAAAAAACCCAACATAATAAATAAGCTTTTGTAATTTCATAAATATATAAACATATAGTTATATAAAAAAAAACTAGTTTTTTTGTCACAGAAAGGAATTAATAAATACTTAAATAACTATTGAACAGTTTGTTGTATTAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24742
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 |
---|---|---|---|---|---|
ENSDART00000113923 | Essential Splice Site | 883 | 977 | 20 | 22 |
Genomic Location (Zv9):
Chromosome Zv9_scaffold3471 (position 96137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 25325419 |
GRCz11 | 6 | 25315980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCTATCCCAAATATCTCTCCACAGAAGCTATTTCCATAATGAGAAGGG[T/C]AAGTTCGGACAAGTCCTGTTCTGCTTTAAACCATTGACCCAAACTACACC
Long Flanking Sequence:
AATTTATTATCTGTAATATTACAATGATTTGAATAATATTATAATTAATCTAAATAATTAATACTAATTTACTAAATAAATACTAATACTAAATAAATGAAAACTAATTTATTAATAAAATAAAGCTAAGCATTAGCTAAAAACGAACACGTATATAAAAGGTCACTTATTTCATTGGCAGTGACTATTTGAACCAAATATGCATGCATAATAGCATTTTGCTTTTGACCTTTTTTTTTTTTTTAATTGGGGTGGTTTTAGAGACATGTAAAAGTATGTATTTTATATTTATGTTTTATGCCAGTGTCAAAGATACCTCTGTAAACAAAAAGTAAAGTAAATGACTTTGAAAAATTGTGTGATAATGGGTCATTTCTTTCTCTATTCTCAGTCCCCTTTCCCTGGTGATGATGAAGAGGAGGTGTTTGACAGTATAGTTAATGATGAAGTCCGCTATCCCAAATATCTCTCCACAGAAGCTATTTCCATAATGAGAAGGG[T/C]AAGTTCGGACAAGTCCTGTTCTGCTTTAAACCATTGACCCAAACTACACCTCATCTTATTCTTCATGACAACCCTTAAAATCCCAACATGGCTCTCTTAGAAAGATCCTTCTCTTTTGTAATCTCATATTAATTATCCAGCTAACTAATGTTTCTAAACATTCTCTTTCTTATCCAGCTGTTAAGGCGAAATCCAGAGCGGCGTCTTGGCGCAGGAGAACGAGATGCGGAGGAAGTAAAGAGGCATCCTTTCTTCAGAGTAGGCCATCTGTTTTACATCGTTTTTTTCTTCTACAGAACATTCACATGTCATTATTAAAATCCTTACCACACTTGTATCCATCTTCCCTCAGGATATGGATTGGCCTGGACTACTGGCAAAGAAGATCCGGCCTCCGTTTGTGCCGACCATCACAAGCCGTGAGGATGTTAGCAACTTTGACGATGAATTCACCTCAGAGGCACCAATACTGACTCCACCTCGAGAGCCCAGGATTCTGA
Associated Phenotype:
Not determined