ZMP
mknk2a
Ensembl ID:
ZFIN ID:
Description:
MAP kinase-interacting serine/threonine kinase 2 [Source:RefSeq peptide;Acc:NP_997888]
Human Orthologue:
MKNK2
Human Description:
MAP kinase interacting serine/threonine kinase 2 [Source:HGNC Symbol;Acc:7111]
Mouse Orthologue:
Mknk2
Mouse Description:
MAP kinase-interacting serine/threonine kinase 2 Gene [Source:MGI Symbol;Acc:MGI:894279]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9168 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19738 | Nonsense | Available for shipment | Available now |
sa11542 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9168
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 |
---|---|---|---|---|---|
ENSDART00000027782 | Essential Splice Site | 80 | 472 | 4 | 14 |
The following transcripts of ENSDARG00000011373 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22465867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23352572 |
GRCz11 | 2 | 23008223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGAAAAAGAGATGCAGAGCCACTGACAGTTTTTCCGGACGTTTTGAAG[G/A]CAAGCGGTTTTGTCWGTCCTCAAGTTTGCAGTTGAGCTTTACTATCTKTT
Long Flanking Sequence:
CGCTCCTTTAAGGTTGGTAGCTTTTTTTTTAAAAATATACTAGACAAAGTTTTGTAAGTGTGAAATGGCAGACTAGGTAACCAAAATGTTCCTGTTGTCCTTTTCCTAGGGGCAAAACCCTTTCAAGACTGATGAATTCATCGATTCGGATTCCCACCTTGAGTCATCCTTCATATTGGAGCGCTCTACAAGGCCTGGTACAGCTGTTTTGCCTGCTGTTTCATTAATATTGACTGCTATTATCAGACTTGCAGGTTGACGTAAATTCTGACGGGGTTAGATAAGGCGTATCTCCTCAAGAACTCATTCTGTGTTAGGCAAAGTTCATGGCAGATTAGAGTGATGGACTTGGCACACATTGTTCATCATAACTGTTGTTTTGTTGTTGTTTCTTACAGCCATGCCTTCCAGCCAGCCCATCGATATCCCTGATGCCAAGAAGAGAAATAAGAAGAAAAAGAGATGCAGAGCCACTGACAGTTTTTCCGGACGTTTTGAAG[G/A]CAAGCGGTTTTGTCTGTCCTCAAGTTTGCAGTTGAGCTTTACTATCTGTTGTGTAAAAAAAAAAAAATACCCCTGTTCTTCTTTACAGATGTTTACAAACTACAAAATGAGGTTCTTGGAGAAGGGGCTTATGCTGTTGTACAGACCTGCATCAATCTGATCACCAATAAAGAATACGCAGTAAAGGTCAGTATCAATTGATGATAATCCAGTATAATGCAAAATGAGCTATAATCAGCGTTCATACTGTTAACAAATAATCAGTTTCTTATCTACATGCAGGTTAAACTCCATTTACTAAAGTTTTTTTTTTTAACATATTGCACCCAGAATGGTTTTAATCCTTTTTAGCAGTGTTTGAAATGGAAGTGATGATTTTACACCTCACTGCACTGATTGTTTTTAAGCAAGTTCAATGTCACTGCAGTCAGAATCTAGGGAGTGAAAGCAAAGTTAATGCACTTTACCCAAATGCTTTTTCATTATACAGTTGAAGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19738
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 |
---|---|---|---|---|---|
ENSDART00000027782 | Nonsense | 349 | 472 | 12 | 14 |
The following transcripts of ENSDARG00000011373 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22479593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23366298 |
GRCz11 | 2 | 23021949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATTGGGCACACATCTCCCCTGCAGCCAAAGACCTCATCACCAAACTAT[T/A]GGTACGGGATGCCAAAGACCGCCTCAGTGCCGCCCAAGTCCTGCAGCACC
Long Flanking Sequence:
ATGTGGTATAGATGAATTAGGTAAACTAACTTGGCTGTGGCATATGAGTGTGTATGGATGTTTCCCAGTACTGGGTTGCAGCTGGAAGGTCATCTGCTGTGTAAAACATTCTGGATAAGTTGGTGGTTCATTCCGCTGTACCGACCCTGATGAATAAAGGGACTAAGCCGAAGGAAAATGAATGAATATCACTGAAAGCATAATATACTGCCTTCCACAGAGCATGCATTGAAGCTAGGATTTTATTTGTCTATTTATTTTTGTTTCTGAGAAAGGAAATGGCCATTTTTTAAATTGAGATTGTGATTTGAGGTTTGGATCATGAGCCCTAGTGATAGTGGTGGTACTAGTGTACTTCAAACATAGTAAATTCTCATTTCTCATCTCAATGCATTCACAGAGCATGCTGTTTGAGAGTATTCAGGAAGGCAAATATGAGTTTCCAGAGAAAGATTGGGCACACATCTCCCCTGCAGCCAAAGACCTCATCACCAAACTAT[T/A]GGTACGGGATGCCAAAGACCGCCTCAGTGCCGCCCAAGTCCTGCAGCACCCATGGGTCAAAGGGGTATGTTGATTTCTTTCCCTCTCTTGGACATTTATTTTACTCTTAAATGTTTTGTTCAACTAAATTCAATAATCTGTCATTTTTCCACTCATTTTGTTTCAAACCCATTCGAAGTTTGTTCAAGAAATTATATTTCAAAATTAACCAAGTTCAAATCGTTTATCGGTACAAAAATTGTTGGACAGCAGACACTACGATTCTGAAATGAGTGTTTGCTCTGCTTCATGCATCACACGTTGCAGATTTCACTGATCATAGAACTAGATTGATAGATGATTGACAGGATGTATTGTGCACCAAATCCTTAAGGGTTATTGTTGCACATTTAAATGTTCCATCTGTGTGTACTGTCTCTCTCAATACACAGACTACATTACTCTACAATCTCGATTTTGAAAAGGAAACTAAAGCATGCGTTTAAAAGTGACTTTACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11542
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027782 | Essential Splice Site | 384 | 472 | 13 | 14 |
The following transcripts of ENSDARG00000011373 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 22480375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23367080 |
GRCz11 | 2 | 23022731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCTTTAGTGTGCACCCAACACTGTGTCTGCATCYATACTACATCAGAG[G/A]TATGTATAGTGCNNNCTTATACTCCTCTAAATCTCATSCAGCAAACATAA
Long Flanking Sequence:
CTGCTTCATGCATCACACGTTGCAGATTTCACTGATCATAGAACTAGATTGATAGATGATTGACAGGATGTATTGTGCACCAAATCCTTAAGGGTTATTGTTGCACATTTAAATGTTCCATCTGTGTGTACTGTCTCTCTCAATACACAGACTACATTACTCTACAATCTCGATTTTGAAAAGGAAACTAAAGCATGCGTTTAAAAGTGACTTTACACAATTGAAGCATTCGAGTGGTGGAACATCTCAAGTTTCATTGAAATGTCTTCATTTGTGTTTAAAAATAGAGTCTCAATGGTTTAAAATGACATGAGGCTACTTAAAGAACTAATCAGATTTTGGGTGTATTGGGAGTTTAATTTTGCCGATTTGTAATAAAAGAACTTAGTCTTTCATGTCGTAGTATCATGTAGCTGTATATCATGTCTTGTGGCTAACTTCTGTTGTACTTCTCTTTAGTGTGCACCCAACACTGTGTCTGCATCCATACTACATCAGAG[G/A]TATGTATAGTGCCTTCTTATACTCCTCTAAATCTCATCCAGCAAACATAAATAGCAGATTAATATTGGCGCACATGACCTTCATTGTGCTCTCTCAGGGGCGGCAGTGCTCAGGACCTGACGTTCTTTGCGGGGCAGGCTGTAGCCATGAACCGGCAGCTGGCAAAGAGGGAGGAGAGTGAGGATCTGTCTCTGTCCTCTCCTCTTCTCTCCAGCAGCTCTGGCTCCATGCTGTTGTCTCCTCCGTCCAGATCCAAGCTGGCCCACCGCAGGAAGACCGCCAGCAGTCAGCACAGAGGACCAGTGTGTGCTGCTGAACTCCGCCAGCTCCTCGCCCCGCTCGTGATCGTGGGCGACTGTGCCTGATTATCATGACCTTCACCAGCCTTCGATCTCCCCTGTCGACCTCTATATGAATCTTCGACTAGGCAGTATGTTGATCCCTGACCTCTCTGCCCACTCGCTTTGTGGGTCTAAAGCGCTTATGGGAAGGACTCGCAT
Associated Phenotype:
Not determined