ZMP
zgc:136354
Ensembl ID:
ZFIN ID:
Description:
mitogen-activated protein kinase kinase kinase kinase 2 [Source:RefSeq peptide;Acc:NP_001038725]
Human Orthologue:
MAP4K2
Human Description:
mitogen-activated protein kinase kinase kinase kinase 2 [Source:HGNC Symbol;Acc:6864]
Mouse Orthologue:
Map4k2
Mouse Description:
mitogen-activated protein kinase kinase kinase kinase 2 Gene [Source:MGI Symbol;Acc:MGI:1346883]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9330 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19265 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45743 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16426 | Essential Splice Site | Available for shipment | Available now |
sa16484 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9330
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100351 | Nonsense | 97 | 889 | 4 | 32 |
ENSDART00000100351 | Nonsense | 97 | 889 | 4 | 32 |
Genomic Location (Zv9):
Chromosome 21 (position 33005649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34005342 |
GRCz11 | 21 | 34039832 |
KASP Assay ID:
2261-5856.1 (used for ordering genotyping assays)
KASP Sequence:
TAGAAATAACAAGTTATGGATCTGCATGGAATTCTGTGGAGGAGGGTCAT[T/A]GCAAGATATTTACCATGGTATAGAATTCAGCAATTTGCTTAATTTTTTTA
Long Flanking Sequence:
TATACTTCTCAGATGTTAATTCAATTAATTGCAAGAATTATTAACTATACAGCAATTTTTTATTTTATTTTTATTCTGGAAAATCAAGATGTTATTCTGAATATTTTTAAAAGATGATTAATTAAAACAAAATTAGAAAAGTTCACAGACCATTATTATTTAACTTTTTTTTTTTTCGATTAGCCTCCTGTCCCTGAGGGTAAGGATGTGCTCATTGTGTCCTTCTTGGTTGTCCACAGGGTGCCAACATTCTTTTGAAATTCTCTGTTTATTTTCTGTCAGGTGATGATATTTCAAGCATTCAAAATGAGATAACCATGATGAAAGACTGCACTCACAAAAACATTGTTGCCTATTTTGGCAGCTACCTAAGGTTAGTTCCACACAAAATTAATACTGCACTATGCAGAGAACTGAAGTAAAACTAACAACAAACATCTTTGTATTTCTTAGAAATAACAAGTTATGGATCTGCATGGAATTCTGTGGAGGAGGGTCAT[T/A]GCAAGATATTTACCATGGTATAGAATTCAGCAATTTGCTTAATTTTTTTAATACTTCATATAATGTATTACTGCATGTGATTTAAATAATTGGACATGTTCTAGGCTATTGTTATTACAATTACATATTATAATTGTCATGTATATGCAAATAATATGACGATCAGTTAATCTGTCAGTTATTTTAATGCTTGATTGATTGGATAGAAAAATTGAAGTGAACATATTTACAACTTAAAATGAACAGGGCTTTGCCATGTTGTTTTTAAAACTTGTTTGAAGTGTATGCATTCACCATTGTTTTCTGTTGTTATTTATGTTGTCTGAAAGAGGGATAATGTTCAAAAGCTCATATGTTAATTTGTCTGTCTAAATGAGGTCATTGTGTTTCTGCAGTCACTGGTCCTCTGAAAGAGAGACAGATAGCTTATGTTAGCAGAGAGACACTTCAGGTGAGAAAGTATTCGTTCATTCGTTTTCCTTCAGCTTAGTCCCTGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19265
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100351 | Nonsense | 97 | 889 | 4 | 32 |
ENSDART00000100351 | Nonsense | 97 | 889 | 4 | 32 |
Genomic Location (Zv9):
Chromosome 21 (position 33005649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34005342 |
GRCz11 | 21 | 34039832 |
KASP Assay ID:
2261-5856.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAATAACAAGTTATGGATCTGCATGGAATTCTGTGGAGGAGGGTCAT[T/A]GCAAGATATTTACCATGGTATAGAATTCAGCAATTTGCTTAATTTTTTTA
Long Flanking Sequence:
TATACTTCTCAGATGTTAATTCAATTAATTGCAAGAATTATTAACTATACAGCAATTTTTTATTTTATTTTTATTCTGGAAAATCAAGATGTTATTCTGAATATTTTTAAAAGATGATTAATTAAAACAAAATTAGAAAAGTTCACAGACCATTATTATTTAACTTTTTTTTTTTTCGATTAGCCTCCTGTCCCTGAGGGTAAGGATGTGCTCATTGTGTCCTTCTTGGTTGTCCACAGGGTGCCAACATTCTTTTGAAATTCTCTGTTTATTTTCTGTCAGGTGATGATATTTCAAGCATTCAAAATGAGATAACCATGATGAAAGACTGCACTCACAAAAACATTGTTGCCTATTTTGGCAGCTACCTAAGGTTAGTTCCACACAAAATTAATACTGCACTATGCAGAGAACTGAAGTAAAACTAACAACAAACATCTTTGTATTTCTTAGAAATAACAAGTTATGGATCTGCATGGAATTCTGTGGAGGAGGGTCAT[T/A]GCAAGATATTTACCATGGTATAGAATTCAGCAATTTGCTTAATTTTTTTAATACTTCATATAATGTATTACTGCATGTGATTTAAATAATTGGACATGTTCTAGGCTATTGTTATTACAATTACATATTATAATTGTCATGTATATGCAAATAATATGACGATCAGTTAATCTGTCAGTTATTTTAATGCTTGATTGATTGGATAGAAAAATTGAAGTGAACATATTTACAACTTAAAATGAACAGGGCTTTGCCATGTTGTTTTTAAAACTTGTTTGAAGTGTATGCATTCACCATTGTTTTCTGTTGTTATTTATGTTGTCTGAAAGAGGGATAATGTTCAAAAGCTCATATGTTAATTTGTCTGTCTAAATGAGGTCATTGTGTTTCTGCAGTCACTGGTCCTCTGAAAGAGAGACAGATAGCTTATGTTAGCAGAGAGACACTTCAGGTGAGAAAGTATTCGTTCATTCGTTTTCCTTCAGCTTAGTCCCTGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45743
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100351 | Nonsense | 399 | 889 | 18 | 32 |
Genomic Location (Zv9):
Chromosome 21 (position 33023304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34022997 |
GRCz11 | 21 | 34057487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTGTGTCCGTAATATCAACAGCACTCACCAAATGAAGAGGATAAATA[T/A]GGGACTGTGAAGAGGATGGCCTCTTCTCCCCAATCAACAGCCCTCTGCCA
Long Flanking Sequence:
ATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTACATTATATTATATTTTTTATATACTGTTTTATTCCAATAGTGCATGATAGATGTTACAGAATATGTATTTATATGTATTTTGCCGGTTTAAAAGACAAATATGATAATCAGCTAATTAATCACAACTTTTTTTCAACTCCTATTTGAGAAATAAATGTGTTCCTAAAACAGTTTAAGGGGAACAAGTAGTCTTTTATAACCCTACTCTGTGCTGTCAAAAGTAATTTTCAATTAAATGAGTGTGTAATAATTATTTCTTATTTTGCAGGAGTTTAACTATAAAGAGGGTCTCTTCAGTTGAGGTAGGAATGAATAAAAATAAGCTTTAAAAGAGACATAGCATAAGTACCATTTATATATTGCTTATTTGTGTCCGTAATATCAACAGCACTCACCAAATGAAGAGGATAAATA[T/A]GGGACTGTGAAGAGGATGGCCTCTTCTCCCCAATCAACAGCCCTCTGCCATCAAGAAAAAAAAGCTCCCACTCCCTCTTCTATCCCCTCGCCTATTATTGGCTCTAGCTCTCTGAAGAACCCTTCCCCCAACACTAACCCTAGCCTACTCAGTGAATCGGCTTTGCTTATTGGTTCAACATTGTCCCACATGTCGCTCATCACAAACTCCTGCCTATTCACAGACTCCTCCTTCCTCAGTCATTCCACCAGTCTAGGTTCCCTCTGTTTAACTCCAACTGAAGGTGAGATCTTTCAGTTCAAAGAATAGGCTAACACTTGAAATCAGAATATCTCTAGAGTTATGCTTTACTAATTTCTATCAGCAGTGTTTTAATTGTATTACATTTAATAACAGAGTACATTATCAACTACATAGTGCTTTCAGGGATTGAACTTACCTCCGTGAAGTTGGCACCCCATAAAAACAAACAATCCCCAAAACTATGCCATTCGTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16426
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100351 | Essential Splice Site | 524 | 889 | 20 | 32 |
ENSDART00000100351 | Essential Splice Site | 524 | 889 | 20 | 32 |
Genomic Location (Zv9):
Chromosome 21 (position 33024883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34024576 |
GRCz11 | 21 | 34059066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCATTACCAAACTTTAATCAGTCTCTCRCAATTTATTACTTATAAAA[G/T]AAAGCTGTTGTCMATGGACTGCCACCTAMACCACAAGTACATGTAAGTAC
Long Flanking Sequence:
CCCCCATTTAATTTTTTTTCTTTTTTAAATATTTTCAAAATGATATTTTACAGAGCAAAGAAATTTTCAAAGTATGTTTGATAATATTTTTTTCTTCTGGAGAAAGTCGTATTTGTTTCATTGCGGCAAGAATAAAAACAGTTTTTAATTTTTTAAAAGCCATTTTAAGGTCAAATTATTAGCCCCTTTAAGCTATATATTTTTTCGTTAGTCTAGAGAACAAACCATTGTTACACAATAACTTGCCTAATTACCCTAAGCTTGCTAGTTAGCCTAATTAACCTAGTTAAGCCTAAACCTAGTTAAAGAAATTTGTTGAAAAAATCTTCTCTCCGTTAAACATAAATTGGGGTAAAAATAAACAGGGAGGCTGATAATTCTGACTTCAACTGTATTTTAAAATATTATACTAATTAATAAAGTCAAACTGTGTTTGAGAATGTCTCAAGGTAATCATTACCAAACTTTAATCAGTCTCTCGCAATTTATTACTTATAAAA[G/T]AAAGCTGTTGTCAATGGACTGCCACCTACACCACAAGTACATGTAAGTACAGAATAATTAGCCCTAATTCTGTTGCATGCCTTAAATTCATGCTTATTTTTCTGTGATGATCCTACATTGTCTTCCAGATGGGGGCCTGCTTCTCCAAAGTATTCAACGGCTGTCCATTAAAGACTCACTGTGCTGTTACATGGGTTCTACCTAAAACCAGAGGTACTTTAGTTAGCAGCTTTTTACTTAAAGTTGCTATTTATATTATAACTTTTTGGGACTAAAATGATCCAAAATCTATTTTTTAACAAGTACATGCCTGTAATTAGAACTGTCCCGATGAGGTTTTTTTGCCCCCGATTCGAGTCATTTGATTTGGAGGATCTACCAATACCTAAACCTGATCCAATACTTTTCTAATACATAAAAAATAATAAAGAAAAGGGAAAGAAACAGATCCAGGATGTTCCTTATTTTTTATTTAATTCACATTTTTGAACATATAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16484
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100351 | Essential Splice Site | 524 | 889 | 20 | 32 |
ENSDART00000100351 | Essential Splice Site | 524 | 889 | 20 | 32 |
Genomic Location (Zv9):
Chromosome 21 (position 33024883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34024576 |
GRCz11 | 21 | 34059066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATCATTACCAAACTTTAATCAGTCTCTCRCAATTTATTACTTATAAAA[G/T]AAAGCTGTTGTCMATGGACTGCCACCTAMACCACAAGTACATGTAAGTAC
Long Flanking Sequence:
CCCCCATTTAATTTTTTTTCTTTTTTAAATATTTTCAAAATGATATTTTACAGAGCAAAGAAATTTTCAAAGTATGTTTGATAATATTTTTTTCTTCTGGAGAAAGTCGTATTTGTTTCATTGCGGCAAGAATAAAAACAGTTTTTAATTTTTTAAAAGCCATTTTAAGGTCAAATTATTAGCCCCTTTAAGCTATATATTTTTTCGTTAGTCTAGAGAACAAACCATTGTTACACAATAACTTGCCTAATTACCCTAAGCTTGCTAGTTAGCCTAATTAACCTAGTTAAGCCTAAACCTAGTTAAAGAAATTTGTTGAAAAAATCTTCTCTCCGTTAAACATAAATTGGGGTAAAAATAAACAGGGAGGCTGATAATTCTGACTTCAACTGTATTTTAAAATATTATACTAATTAATAAAGTCAAACTGTGTTTGAGAATGTCTCAAGGTAATCATTACCAAACTTTAATCAGTCTCTCGCAATTTATTACTTATAAAA[G/T]AAAGCTGTTGTCAATGGACTGCCACCTACACCACAAGTACATGTAAGTACAGAATAATTAGCCCTAATTCTGTTGCATGCCTTAAATTCATGCTTATTTTTCTGTGATGATCCTACATTGTCTTCCAGATGGGGGCCTGCTTCTCCAAAGTATTCAACGGCTGTCCATTAAAGACTCACTGTGCTGTTACATGGGTTCTACCTAAAACCAGAGGTACTTTAGTTAGCAGCTTTTTACTTAAAGTTGCTATTTATATTATAACTTTTTGGGACTAAAATGATCCAAAATCTATTTTTTAACAAGTACATGCCTGTAATTAGAACTGTCCCGATGAGGTTTTTTTGCCCCCGATTCGAGTCATTTGATTTGGAGGATCTACCAATACCTAAACCTGATCCAATACTTTTCTAATACATAAAAAATAATAAAGAAAAGGGAAAGAAACAGATCCAGGATGTTCCTTATTTTTTATTTAATTCACATTTTTGAACATATAACAT
Associated Phenotype:
Not determined