ZMP
mknk1
Ensembl ID:
ZFIN IDs:
Description:
MAP kinase-interacting serine/threonine-protein kinase 1 [Source:RefSeq peptide;Acc:NP_001108211]
Human Orthologue:
MKNK1
Human Description:
MAP kinase interacting serine/threonine kinase 1 [Source:HGNC Symbol;Acc:7110]
Mouse Orthologue:
Mknk1
Mouse Description:
MAP kinase-interacting serine/threonine kinase 1 Gene [Source:MGI Symbol;Acc:MGI:894316]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14337 | Nonsense | Available for shipment | Available now |
sa6198 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35046 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41797
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 |
---|---|---|---|---|---|
ENSDART00000123257 | Nonsense | 78 | 461 | 4 | 15 |
ENSDART00000125371 | Nonsense | 76 | 459 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 13366941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13123764 |
GRCz11 | 11 | 13181423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGAATGGAGAGCAGTCAACCAATCAGCATCACAGACCCAAGTTCACGC[C/T]GAAAGAAGAAACGCAGAAGAGCCGGAGACAGTTTCACAGGCAAATTTTGT
Long Flanking Sequence:
AAAGATCCAACATCTGCAAAGTCATCTTAGATTAAGCAATGTATGGAGAATGGACCCCAGATCAGTTTATGAAGATTTCTTAGTTATTGTTTAAAATCAGTTCCCCTTTGTAATGAAGAAAGTTTTTTTTTTTACTTTGGGTCTTACTGCTGGTCCATGTACAGTATAACTCTGTAAGAATTAGAACGTTGATGTTGTGTTCTGTTATTAAAACTTTGTTTTATTCTTCCAGATATCCAGTAGCATTCTGGGATCGGGTAAGGTGGAGAGCCGTGGTTCGCTCTCTCGTGTCCCCAGTACCGTCTCGCAAACCTCTACAGGTACAAAGACATTCTGCCAATCATGACATTACTCCAGAAATGAAGTTCTCACAAAAGAATCTTTGAAGTGGACTTTATTATTATTATTATTATTATAGTTATTATTCTTTTTAATATTATTATATAGGATTAGGAATGGAGAGCAGTCAACCAATCAGCATCACAGACCCAAGTTCACGC[C/T]GAAAGAAGAAACGCAGAAGAGCCGGAGACAGTTTCACAGGCAAATTTTGTGGTAATTTATCATCTTGAACATTCCAAAAAATGAGCTTTTCTTTCTAATGTGTCTTCTGCACTATTCCATCTGTATAATCTGTGGTGTGCATTATCAGATCTTTCAAAACATTTGACTGCATTTCCTTACTATACTTTCTGATTGGAATATGTGTGTTGTCAGCTCAGAAGTGCGTGTGTTTCTGTTTTAGATCTATACAGGCTGACGGATGAGCTGCTGGGTCAGGGAGCTTATGCCAAAGTCCAGGGCTGTGTGAGTTTACAAAATGGCACGGAGTATGCGGTAAAGGTGAGATGATGTCAATGTCACATCCTCAAAATAGTCACATTGCAAGATAAGCAATGTTGAGTCTGAATTATAGTTCAGTAGGAGCTACAGAAATTTATTTATTTACTGTATTTATATAGAATTATTACAATTTATGTTAAAAAAAATCTTAGAAATGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14337
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 |
---|---|---|---|---|---|
ENSDART00000123257 | Nonsense | 109 | 461 | 5 | 15 |
ENSDART00000125371 | Nonsense | 107 | 459 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 13367226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13124049 |
GRCz11 | 11 | 13181708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTTAGATCTATACAGGCTGACGGATGAGCTGCTGGGTCAGGGAGCTTA[T/A]GCCAAAGTCCAGGGCTGTGTGAGTTTACAAAATGGCACRGAGTATGCGGT
Long Flanking Sequence:
TCGTGTCCCCAGTACCGTCTCGCAAACCTCTACAGGTACAAAGACATTCTGCCAATCATGACATTACTCCAGAAATGAAGTTCTCACAAAAGAATCTTTGAAGTGGACTTTATTATTATTATTATTATTATAGTTATTATTCTTTTTAATATTATTATATAGGATTAGGAATGGAGAGCAGTCAACCAATCAGCATCACAGACCCAAGTTCACGCCGAAAGAAGAAACGCAGAAGAGCCGGAGACAGTTTCACAGGCAAATTTTGTGGTAATTTATCATCTTGAACATTCCAAAAAATGAGCTTTTCTTTCTAATGTGTCTTCTGCACTATTCCATCTGTATAATCTGTGGTGTGCATTATCAGATCTTTCAAAACATTTGACTGCATTTCCTTACTATACTTTCTGATTGGAATATGTGTGTTGTCAGCTCAGAAGTGCGTGTGTTTCTGTTTTAGATCTATACAGGCTGACGGATGAGCTGCTGGGTCAGGGAGCTTA[T/A]GCCAAAGTCCAGGGCTGTGTGAGTTTACAAAATGGCACGGAGTATGCGGTAAAGGTGAGATGATGTCAATGTCACATCCTCAAAATAGTCACATTGCAAGATAAGCAATGTTGAGTCTGAATTATAGTTCAGTAGGAGCTACAGAAATTTATTTATTTACTGTATTTATATAGAATTATTACAATTTATGTTAAAAAAAATCTTAGAAATGTTTGTCTTGTTTCTAGTCCAAATATCTACATTTATAAAATATAATATATTATAATAATACAAATATCCACACAAAGTGAAACGAGATTATTTTACTTACCCCACTGGCAGATAATTGTGCTTGTTTTAAGAAAACTTTTTTTTTACTTATTACTTTTGAATATTTTTTACTAGATCTAAGTATTTATATATTATATATTTATATATTATTTGGACTAGAAATGAGACAAAGTAAGAAAAGCAGTTTTTGCATTATGATTTATTCAATTTCTCCAGCTAAATACTGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6198
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 |
---|---|---|---|---|---|
ENSDART00000123257 | Nonsense | 188 | 461 | 8 | 15 |
ENSDART00000125371 | Nonsense | 186 | 459 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 13368354)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13125177 |
GRCz11 | 11 | 13182836 |
KASP Assay ID:
554-5139.1 (used for ordering genotyping assays)
KASP Sequence:
AAATATTTTCTKTTGTCCTCCTAGGTTCCATTTTGACACACATCCAGAGT[C/T]GAAAATACTTYGAYGAGAGAGAAGCGAGTCGTGTGGTCAGGGATATAGCA
Long Flanking Sequence:
TCATGTCATTATATCATAGTATTTGACTTCTAACTCTTAAAAACTTAGATTTTGTCTTAAAATATTGAATTAGTTTTCTGTACACAAACATAATGTTTTACTTTGTATAACTTGGCTGTGCTTCTCAGATAATCGAGAAGAATGCTGGTCACAGTCGCAGCCGAGTTTTTAGAGAGGTGGAGACGCTTTACCAGTGTCAAGGAAACAAGTAAGATCATAGTCCAAACACTCCACCAGCTATTTTATTCAATAAAATAATTTCAGAATTATTGTTATTGATAGAAGTAAGTTGTAGAAATTACTGTGTTTCTCTCACAGGAACATTCTGGAGCTGATTCAGTTTTTTGAAGATGACAGCTGCTTTTATCTGGTGTTTGAGAAGTTACGTGGAGGTATCGTTCATCATTGTAGCTGAGTAATACAAAAATGCTTATTCCACCTTTTTTTTCTAAATATTTTCTTTTGTCCTCCTAGGTTCCATTTTGACACACATCCAGAGT[C/T]GAAAATACTTCGACGAGAGAGAAGCGAGTCGTGTGGTCAGGGATATAGCAAATGCACTAGACTTTCTGCACAACAAAGGTAAACATTGTATGTGTACTCTACAGCCTACTAACCATGAATCAGCATCAGTCTGTTTATTTACACTTGTCTCTATTTTTCCCACAGGAATCGCCCACCGTGATCTTAAGCCTGAAAATATCCTCTGTGAATATACTGATAAGGTAACACATGCCTTTAGAGATTGGTAACATTGTGTTGGCTGTCTGGCCTAGAGAAACTACAGTGCAAACTGAAAATTGCATCATTTTATGTGAAATATATAACGTAGAGCAAAATTTGGGTCTGTTTGGGTTTCGTATTTTTTAAGTAGTGCCTTAAATTCACTGAAAATATACTGAATTGGTAAAAAAAAAAATTTTGGAAAACATTTACAGTAATAGAAAAAAACTTGTCTAAAATAACTTAATGCATTTAAAAATGCTATAAATTTCTTTGTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35046
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 |
---|---|---|---|---|---|
ENSDART00000123257 | Nonsense | 423 | 461 | 14 | 15 |
ENSDART00000125371 | Nonsense | 421 | 459 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 13373956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 13130779 |
GRCz11 | 11 | 13188438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGCAGTTTGCAGCTGAAGCCATCGCGTTTAACCGGCAGCTGTCGCAA[C/T]AGGAAGAAGAGCAGGAAGACTTTGGCGCTGTCGTCTGCTCCATGAGGCTT
Long Flanking Sequence:
GATAGATTTGTGAGGGGTGTACATGTATATGCTGCACACTGTATAACTTTAACATATTTTTAATTATTCCTGTGATTTATTACTGTGATTCCTATTTAATTTATTCCTGTGATGGCTAAATCGCTTTTTAAAATGTTCAAGTAAATATTACATAATGTAGCTATTTATTAAAAATGTATTTACATTTTTTTATCAATCAAGGGCAACTAAACGCAAAATAATGATTAGTAGTTTATATTATACAAACTAAATGTAACCATTTGGTGTTTGCTTTAAATATAATCATATTTATTTGTTTTCCAGAATGCACCTGAAAGAGTTCTTCCAACTCCTCGTGTTCTACAAAGGTATTTTTATATTTTTTCAATTCAGATGTATGGTTTCCAAATTTCTGTAATGTTTTTAACAGTGTCTCTGGTTGAACGCACAGAAACTGCAGCACTAAAGATCTGACGCAGTTTGCAGCTGAAGCCATCGCGTTTAACCGGCAGCTGTCGCAA[C/T]AGGAAGAAGAGCAGGAAGACTTTGGCGCTGTCGTCTGCTCCATGAGGCTTTCTCCGCCTTCTAACTCTAGACTTGCCCGTCGTCGAGCACAGTCTCAAGCACTACGCAACAATACCTGAAGTCAACCCGCTGCACAGGTGCATTATAACCGTTCAGACACTTCAGAAACACACAAATGCGCATGCACCAGGTACTACCAGACTAACCTTATGTGTACTAAACCATGCACACGTCTTTAATTCATTTCGCAGGTCTGCTTGGTCGTCTTTCTGTTCACCTATTGTGGGTTTGGTATCAGAATGTTTATAATTATCGTCATATATTTATGGCTGGTGGTGATTGTTAGTCAGATATAAAAAAGTGCTCGGCTATGTGGGAGGGAATAGACCATTTTATTTTAATGTAACGATGACATTCGCATCGCTTTTAAATGTAAGTTAGCGTTTCTATTCTTAAAACAAGTTTTATTATTTTTAAAAACCACTTTAGTTACTGTGAAG
Associated Phenotype:
Not determined