ZMP
mapkapk2b
Ensembl ID:
ZFIN ID:
Description:
mitogen-activated protein kinase-activated protein kinase 2b [Source:RefSeq peptide;Acc:NP_00109527
Human Orthologue:
MAPKAPK2
Human Description:
mitogen-activated protein kinase-activated protein kinase 2 [Source:HGNC Symbol;Acc:6887]
Mouse Orthologue:
Mapkapk2
Mouse Description:
MAP kinase-activated protein kinase 2 Gene [Source:MGI Symbol;Acc:MGI:109298]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1101 | Nonsense | F2 line generated | Not yet available |
sa9002 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21345 | Essential Splice Site | Available for shipment | Available now |
sa18024 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1101
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000003954 | Nonsense | 56 | 397 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 38577742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37433157 |
GRCz11 | 8 | 37465591 |
KASP Assay ID:
554-1003.1 (used for ordering genotyping assays)
KASP Sequence:
TCAAAAAGAAAGTAATAACAGAGGAGTATAAGCTTGCAGGACAAGTACTC[G/T]GAATAGGCATTAATGGAAAGGTTWGGGAGATATTCCAGAAGAAAAGTGGC
Long Flanking Sequence:
CTGGCCATTGAGCTGAATTTGTTATGATAACCTGGCAACCCTTGTTTGTCAGAATGTGTGGTAATCTGTTTTACAGTTAAAGTGTACTGTAACTGACCACTGTCTTCAAAACTAAGAAGGTAAATAAATGAAAAGATATTTAACAGTTATGTCCTCTAAAGTAGCCTAATTCTACCAAAATTCTGGCTGCTTTAAATCATCAAGTGCAAAAAATAATACAGAGACATCTGTGTAAGAGAAGTGCTAACCAGCTCTTAATTGGATCCTTTAAAAATCCTTTAAGCTGGTCTAAAGAAGTTGTGCTGCACAGTCCGGGATGAACACAGTCTACCACTATGTTGGATAATACAGAAGATAAAAAGGAATCAGATTTTTCCAGTGAGCAGCAAGGGACTCAGTCTCCGATTAATGTTTTGCTTTCAGAGTCGGTGCTCAAACCTACATTGAAGATCAAAAAGAAAGTAATAACAGAGGAGTATAAGCTTGCAGGACAAGTACTC[G/T]GAATAGGCATTAATGGAAAGGTTTGGGAGATATTCCAGAAGAAAAGTGGCAGGCACTTTGCTTTAAAGGTAAGCCACCTATTTAGTTTATTTTTATTAGGCAGCTTCACAACCTAACATTATTTTTTTACATTTTCCACAGCAAAGATAGGAATGGCTGTTGGTCAAAGATTTTTGTTTACAGTAAAGTCTTGGTTCAGTTATCAATTTCTCCCCCCACCCCCATTCTGCTACATAGTTTGAGTCCACATCAATAAATCTCTTTGGTAAATAGGATCATTCTGGTATTTCTGGGAACAAACTGATGTTTCTATGCTGTAAAAACTAACAGTGCCTCAAATATTGTATTGTGTTGTATAAGTGCCTCAAAACCTTTTCTATTAGAGTTACAGGAGGGGCTGTTAACATTTCTGCCAAGAACTTATGGCATCCATTAAGTACTTAAACTATAGACTTTGTAAATTCCTTCTGCCAAAACATTCATCATTGGTTCTGCGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9002
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 |
---|---|---|---|---|---|
ENSDART00000003954 | Essential Splice Site | 173 | 397 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 38579857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37435272 |
GRCz11 | 8 | 37467706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTGTTGAGTTTCTRCATGGTATCAATATTGCACACAGAGACCTCAAG[G/A]TAAGCAACTCTATAGCCAAAWATCTGAYATTTATTTTAGGGTTATTACAG
Long Flanking Sequence:
CTTTATAGTACAAAAGTGGACAAAAAAGGTATAAAAGTGTACCTTTAAAAAGGTACCACACCAGTAAAACCTTTTGTACCTTTATTTCTGAGCGTGCAATATACTGAATTATCTTCAACAGATTAGATTACTTTTTTGGCTTTTTATTTTTTTTTCAAATAGCTTTTAGATTTCTTTTCCTCATATAAGTAAAAAATCCATTATTATTTTTAACCTTAATGCAATCTGTTACTTAAACAGTATGGAAGGGGGAGAACTCTTTCGCCACATTCAAGAACGTCGTGATCAAGCCTTCACTGAAAGAGGTACACATCAAACCCATACACACACACTGTCAAAAACATAGTTGAGAAAACTGATCACATCACAGAAATTAATTGTCTTCTTCCCCTCTTTTTATACTTTCCTAACAATGGGTAGAAGCCTCCGAAATAATGAGAAGTATAGGAGAAGCTGTTGAGTTTCTACATGGTATCAATATTGCACACAGAGACCTCAAG[G/A]TAAGCAACTCTATAGCCAAATATCTGACATTTATTTTAGGGTTATTACAGAATATGTTTATTTTACTTTAATTCTGTTCTTTTAAATGTCATACAATTACCCCTAAAACAATTGATAACATTCCACAAAAATATTAATGCTAAACTAACAAATGTTGCAACAAATCATCAGTAAATGAAAATGATTTCTAAAGGATCATGTGACACTGAGGTCTCTATCAAACACCTGGTACAATATAGCGCAAGATCTGTTTGGTACGATTTGTTGCTATTTTCAGAAAAAAAAAAAAAAAACGCAACCCTAATTTTTAAGTTTTATGCCGCATTCTTTAAATTGTAATTTAAAATTTAGAAATAGCTTTGAAACAAATCTTTGCTCTTAACAAAAAAAATTAAATATGTAGGCTAATGAATGTCTTTAGTGGAGTGCGTACAACACCGTTTCCTTATCAAAGTAAAGAGTAAAGGTAAAGTTAAAAGAAGATAAAGAGGCCGAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21345
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003954 | Essential Splice Site | 216 | 397 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 38581584)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37436999 |
GRCz11 | 8 | 37469433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCCAACAAATGCTTGACCACCCCATGTTATACACCTTATTTTGTTGG[T/A]AAGCAACCTTTTTGAGTCTCGATTGGAATCATAACACAATGATGCTGACA
Long Flanking Sequence:
TGGGTTATGCAGTGATTTCCATTTTAAAATATATTTATTTCCATTTAAAAACACATTACTTCATACATGACAGTTTGATTATTGCATTAAAGCTATGAAACTGAGGAGACATTCTCAGGACAAGTTCAAAACTCAGCATTAAGTTCTAATAAAAGTCTAATAGTATGATTAAAACCATAAAAAAAAAAAAAAACATCCGAATATTTTACCATGTATTACTTGTGTCCAAGTCTTCAAAAAGTTGTGTCTTACATCTATAGAAGAAGATATCTTTCCTGCTAAAATATATTGAAACAACAGTCAAACTGTTACAACATATTTTTACATATTACAATATTCAACTAATTAATTAATACATCTTTTATATGGCAGCCAGAAAATTTACTGTATTCATCAAAGCAGCCGGATGCCCAACTCAAGCTTACAGATTTTGGATTTGCCAAAGAGACCACATCCAACAAATGCTTGACCACCCCATGTTATACACCTTATTTTGTTGG[T/A]AAGCAACCTTTTTGAGTCTCGATTGGAATCATAACACAATGATGCTGACAACTGCTTTCTTTTTCAGCCCCGGAGGTGCTTGGTCCAGAGAAATATGATAAGTCATGTGACATGTGGTCATTAGGGGTCATCATGTACATCTTGTGAGTGTAAATTATATTAGTTCCTTATACTGTGATATTTTTAATTTAATTTATAACCAACATATATCCTCTTAGATTGTGTGGATATCCACCATTCTATTCAAACAATGGCTTACCACTGTCACCGGGAATGAGAAAACGAATACGGAATGGCCAATATGAATTTCCAAATCCCGAGTGGTCGCATGTGTCAGAGGAAGGTAATTGTATTATATGAACATGTTTGTTCAATATTGCAAACAATATTACTCACTGTGTGTTTTTTCTCTCTTATTTTTTTTTTTTTTTTTTTAGCAAAACAGCTCATTCGACAGCTCCTGAAAACAGATCCTACAGAGAGAATGACCATCACAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18024
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 |
---|---|---|---|---|---|
ENSDART00000003954 | Essential Splice Site | 283 | 397 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 38581929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37437344 |
GRCz11 | 8 | 37469778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCAATATGAATTTCCAAATCCCGAGTGGTCGCATGTGTCAGAGGAAGG[T/C]AATTGTATTATATRAACATGTTTGTTCAAKATTGCAAACAATATTACTCA
Long Flanking Sequence:
TTAATTAATACATCTTTTATATGGCAGCCAGAAAATTTACTGTATTCATCAAAGCAGCCGGATGCCCAACTCAAGCTTACAGATTTTGGATTTGCCAAAGAGACCACATCCAACAAATGCTTGACCACCCCATGTTATACACCTTATTTTGTTGGTAAGCAACCTTTTTGAGTCTCGATTGGAATCATAACACAATGATGCTGACAACTGCTTTCTTTTTCAGCCCCGGAGGTGCTTGGTCCAGAGAAATATGATAAGTCATGTGACATGTGGTCATTAGGGGTCATCATGTACATCTTGTGAGTGTAAATTATATTAGTTCCTTATACTGTGATATTTTTAATTTAATTTATAACCAACATATATCCTCTTAGATTGTGTGGATATCCACCATTCTATTCAAACAATGGCTTACCACTGTCACCGGGAATGAGAAAACGAATACGGAATGGCCAATATGAATTTCCAAATCCCGAGTGGTCGCATGTGTCAGAGGAAGG[T/C]AATTGTATTATATGAACATGTTTGTTCAATATTGCAAACAATATTACTCACTGTGTGTTTTTTCTCTCTTATTTTTTTTTTTTTTTTTTTAGCAAAACAGCTCATTCGACAGCTCCTGAAAACAGATCCTACAGAGAGAATGACCATCACAGAATTCATGAAACAACCTTGGATCAGTGTGAGTATTGACATTTTTAGGGTTCTCAAGCACATTTTAAATGAAGAGTTGAGCACTTTTAGCTTAGCAAAAATCATTGAACTAGACAGTTAGCATCTTGCTGGAAGAGTTTCACTAATTTTCCTATTCAAAGCTGGACTATTCATCAGTTACATCTTGTACTAAGGCCTATGGAAAATGGAAAGTCATATTTTCTACTCCAATATGTCTAGAAACTTTACTCTCATTCTAGCATAATATCTTAGAAACTTGCTGCCGTACCATGACTGCAGCTGGCACAATGCAGCAGGCATTACCTAGTTACCCAGGGAATACATAATAT
Associated Phenotype:
Not determined