ZMP
map3k9
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens MAP3K9, mitogen-activated protein kinase kinase kinase 9 (MAP3K9)
Human Orthologue:
MAP3K9
Human Description:
mitogen-activated protein kinase kinase kinase 9 [Source:HGNC Symbol;Acc:6861]
Mouse Orthologue:
Map3k9
Mouse Description:
mitogen-activated protein kinase kinase kinase 9 Gene [Source:MGI Symbol;Acc:MGI:2449952]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12907 | Nonsense | Available for shipment | Available now |
sa35552 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45495 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31945 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12907
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057185 | Nonsense | 131 | 1024 | 1 | 11 |
ENSDART00000146522 | Nonsense | 119 | 554 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 36585672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36058241 |
GRCz11 | 13 | 36184073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGYAACGGAATCTCGGAGAAGATCCGGGACACGCCGGAGGACTATTG[C/A]GACTATTCGGTGCCACCGTTACACTGTGAGTACGCTGAYCRCATCTACAG
Long Flanking Sequence:
GGAGGGCGGCAGGTCTGGAGCTCGTTGAGGCGAGAGGCTGCTCGGATTAACCGCTACTTATGCTGCGGCTTTGCGCCCGGTCTTGAGCTCTGCGGCAGGTGAGGAGCAGCAGAACCGGGCCGGTCGCCCCTATGGATCGGCAGCATGGATGCTTTCAGTTTCCCCTTTAACAGCAGTGGCCCGGACAGCGCAGACGGAGATGGAGCCGCCGCAGAGCCTCAGCCGGGGGCTCGTCTCCTCGGGTTTGGCCCTGCGGCGGCGGCGACCCCATCCGGTGCCGGTTACTGGACCGCCGTGTTCGACTACGAGGCGACCGCCGAGGACGAGCTCAGCCTGCGGAAGGGGGATCGGGTAGAGGTGCTGTCCAAGGACTCGCTGGTGTCCGGGGATGAGGGCTGGTGGACAGGTATGATCGAGGACCGGGTCGGTATTTTCCCTAGTAACTACGTGAGCAGTAACGGAATCTCGGAGAAGATCCGGGACACGCCGGAGGACTATTG[C/A]GACTATTCGGTGCCACCGTTACACTGTGAGTACGCTGACCGCATCTACAGAAAACATAAAGGTGTCTGCAGAGGGTTGAGTTGATTTGGCCCACACTGATCTATAATCACTTCAACACACCTTGATTGTTCTGGTTAAAGGGTAGTTCACCCAAAAATGAAAATTTACTATTTAGTGTGATTTAAGTGGTTCTAGACCAGGGATGGGCAAACTTGATCCTCGAGGGCCGGTGTCCCTGCAGAGTTTTGTTCCAACACTAGTCAAACACACCTGAACAAACTAATCAGTGTCTTCAAGATCACTAGAAATCTATAAGCAGGTGTGTATAATTAGAGTTGGAGCTAAAATGTGCAGGGCATCGGCCCTCCAGGACAGAGTTTGCCCACTCCTGTTCTAGATCTTTATGAGCTTCTTTCTCCTGTTGAACTCAAAATAAGATATTTTGAAGAAAGCTGAAATCTTCCATAGGTACAAATATTGTTACAGGTTTCCTGCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35552
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 |
---|---|---|---|---|---|
ENSDART00000057185 | Nonsense | 345 | 1024 | 4 | 11 |
ENSDART00000146522 | Nonsense | 333 | 554 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 36572291)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36044860 |
GRCz11 | 13 | 36170692 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGTCTGTCTGTCTGTCTTTTTCTCTCAGTTACGGGGTTTTGTTGTGG[G/T]AGCTGCTGACAGGAGAGGTGCCGTTTCGTGGTATTGACGGTCTGGCAGTG
Long Flanking Sequence:
ATATAATTATAAAAAAGATGTATAATATGTATTTAAGTATTAATAAACCAAGTTATTAAAATAAACGATAGAGCATAATACAAAGTGACAGACTTTTTATTTTTTCCCTACAATATACCGTATATCATCATATTGCACAGCCCTAATTAGATCTGGAAATCTGCATATTTATCACATGCAGCAGATTTCAATCTTCCCAAACCGTGGCCAATGTATTTCTGTCAATATTGTCAACATCTCTTGCCCATTTATCCACTGAAGCGCTTATTTTATGTTTTAAAGTACATGACACTGCAAAGGCTCACTTTGAAATGATAATAGAGAGATTTTCTGTTTTCACAATAGCTGTCATCCATTTGTGGTGTTTCTGTGTAGGATTCTGCTTGTTCCTGCACAGATACTGTTGGTGACAGCTTGTCGTTGTGGGTAGTCTTGTTTTAACTGCAGAGTCTCTGTCTGTCTGTCTGTCTTTTTCTCTCAGTTACGGGGTTTTGTTGTGG[G/T]AGCTGCTGACAGGAGAGGTGCCGTTTCGTGGTATTGACGGTCTGGCAGTGGCTTATGGTGTGGCCATGAATAAACTGTCCCTGCCCATTCCCTCCACCTGTCCTGAGCCGTTCGCCCGGCTGATGGAAGGCAAGAAATACTGCTGCACTCTTTGTTGAAGAAATAGTTCACGCCAGTATGAAAAATGACAATTTTTTTACTCACTCAAGGTGTTATAAACCTTAATGAGTTTCTCTATACTGTTAAACACAAAAGAAGATATTTTGAAGAAAGCTGAAAACCTGTAACCATTGACTTTCATTGTATAAAAAGCTAATACTACGCAAGTCAATGGATACAGGTTTCTAGATTTCTTCAAAATATCTTTTTTGTGTTCAACAAAGAAAGAAAGTCAAACAGGTTTGAAACAAGTAAAGAGTGAGTAAATGATGGCAGATTTATTTATTTGTTTATTTTTTCGATTGAACTATTTCTTTAACTCAGTGCTTCTTTTATGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35551
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 |
---|---|---|---|---|---|
ENSDART00000057185 | Nonsense | 508 | 1024 | 6 | 11 |
ENSDART00000146522 | Nonsense | 493 | 554 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 36567594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36040163 |
GRCz11 | 13 | 36165995 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACGTCATCATTCACCAGCTGTACCAGGAGAAACCACGAGTGCAGCAC[C/T]GACACGGAAAGTTCCGGCGCAGTCGACTTAAACTGCGGGATGGGAACCGC
Long Flanking Sequence:
GAGGAAACCCACACCAACCCAGGGAAAACATGCAAACTCCACACAGAAATGCCAATTGACCCAGCCAGGACTCGAACCAGTGACCTTCTTGCTGTGAGGTGACAGTGCTAACCACTAAGCCACCGGGCTACAATAAAATTGTTATTTAATAAATCTAAACTTTTCTCTTTGTTGTGGTGGAGTTAAACTCAATATGCTCTTTCATGGATGCTCCACAGTAATGCTCCTTAATGAACGTGTCCCAGATGAATTTACCAGATTATCCACATGACACAGAGCAGAATGATGAGTAAGCTAGATCTCTCAAGTTGTCTTTCTTGCTGTAGGAGTTGAGATCCTGGGAGGAGGAACTGAGTCGTGCAGCTCTACAGCAGAAGTACCAGGAGGAGGCTTTACGGCGACGAGAGCAAGAGCTGGCAGAGAGAGAAATTCACATCCTGGAGCGAGAGCTCAACGTCATCATTCACCAGCTGTACCAGGAGAAACCACGAGTGCAGCAC[C/T]GACACGGAAAGTTCCGGCGCAGTCGACTTAAACTGCGGGATGGGAACCGCATCAGCCTGCCTTCTGGTTAGTATTTTGTTAAAGTTAGCAGGAAATGGAAGTTGTGAGTGTATTTTTTTCTCCATTGTGGTGTACATTTAACGGCCACTTTATTACGTACACAATACTAGTACCGGGTTGGACCCCCTTTTGCCTTCAGTACTGCCTTAACCCTTCCGTGGCATAGATTCAAGAAGCTACTGGAAATATTCCTCAGAGATTTTGGTCCATATTGACATGATAGCATCAAGGGGTTGCTGCAGATTTGTCGGCTGCACATCCATGATGTGAATCTCTCGTTCCACTACATCCCAAAGGGGCTCTATTGGATTGAGACCGGTAACTTAGGAGGCCATTTGAGTACAGTGAAATCATTGTCATGTTTAAAAAACCAGTCTGAGATGATCCGTGCTTTATGACCAGTCTGGCCATTCTCCTCTGACCTCTGGCATCAACAAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45495
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 |
---|---|---|---|---|---|
ENSDART00000057185 | Nonsense | 821 | 1024 | 10 | 11 |
ENSDART00000146522 | None | None | 554 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 36563705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36036274 |
GRCz11 | 13 | 36162106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGCTGCTCGTGCTGCGGCCCCCGACTCCCCCAGCCCTGCCCCCTGGA[C/T]AAACCCCACCTCCTCTGAACCCACTGGTCAACACCCACCTGGAGAGCTTT
Long Flanking Sequence:
GCTTCCCATCAGAGTCAGCTGACTCCCCTGGCCAATCATACCTCTGTATCCCATTCCACAGGGATGGATCTGCTTCAGACAGTTATGGCGTGGAGAGCGGCACGACTGGAACAGCTTCTGACGTTTCCCCCAGTTATACGCGGAGAAGTCCCAGTGGAAATCGTCGATCAGAGCTGGTGTTGCTGGGCTGCGGGGCAGTTCTGGCTGCTGTCGGTTTGGGTCATAACCTGCTGGACCTGATGCGTGTAGAAGAGTGTGTGCGTCCACGATGGGAAGGGCTGTTTCACCGTACTGGGGGTCAAAGTCGTGGTGCCAGCCCACCCACACGCAAACTCTTTAAAAGGGAAAGCCCTCGTCGGCCACCGCCACTGCCCACCTCCCTCACACTTCTGTCTCTCTCATCGGTGTCTGATTGTAACTCAACTCGTTCTCTCCTGCGCTCCGACAGCGAAGAGCTGCTCGTGCTGCGGCCCCCGACTCCCCCAGCCCTGCCCCCTGGA[C/T]AAACCCCACCTCCTCTGAACCCACTGGTCAACACCCACCTGGAGAGCTTTAAGCGGCACCCTCGACAGTCTCTGACGCCCACACACGTGCCCTCAGCGCCCAGTGCTGCCTGCAGGCTTCATCGCACGCCTTCAGATGGTGCAATAAAGATGAAGTGCTCGCCTGCACATAACAACCACAACCCCACCCCAACTACCCCCTCCAAAAATACAGGTGAGAAATTCTTCCAAACCTCTGCATTGTTCATTTATTATAAAATAGATCAGTACTGCCCTGAACTTACCTTGACAAAAGAATAACAAACAACAAATTATGAATTGTAAACTGCATACTACTCTATTCCTGAATACCTCTATTCCATAGAATGATACGGTAAATATATGATAGTTTGCTGAATTCAGTTTCAAATTCAACGTCAAGGTCAGGTAGTCTTTTAGAAAGTTAGATCGTTAATATTTTTGGCCAAGAAAAGTTAGAGCAAACAAAAACAAAGCAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31945
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 |
---|---|---|---|---|---|
ENSDART00000057185 | Nonsense | 992 | 1024 | 11 | 11 |
ENSDART00000146522 | None | None | 554 | None | 7 |
Genomic Location (Zv9):
Chromosome 13 (position 36561733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36034302 |
GRCz11 | 13 | 36160134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAATGGAGCAGCCAACCCCCTGTTCCCCTTGGGTGAATGACAGTCTTT[T/A]GGACCAACAGGATGAAGGCCAATACAAGGATGGGACACGACCACTCTCAT
Long Flanking Sequence:
AGTTTAGTTTCAACCCTAATAAAACAAACCTGATTAAACTAATTGAGTCCTTCAGGATTGTTTGAAACCTACAGGTAAGTGTGTTGAAGCGGGGTTGAAACTAAACTGGAGGGCTGCGGCCCTTCAGGAACTGGCTTTGACACCTGCCTTAAATATTCTTCATATGCTATTTTGTAAAGTCTTTTCTGCCCTATGTGCAGTTACTCAGTGGACTTTAAGTGAGGACCCTTCAGAGGTGCCCCGTCTTCCTGATCCAAACCTCATCTTCCCACCTACACCACGTCGGCGCTTCCAGCCGGAGCGTCCCAAGACTCTGGACTTTCTGGCTAGGCCTCGACCATGTCCACGCGCTCGTTGTGGGTCGCAGTGGGGCGAATCTCCTGCTCACACATCCAGCACTGAAACCCCATCCACTGTGGAGTTTGGCGGAGGTGTGGCCGTCCTGCCCACTCCAATGGAGCAGCCAACCCCCTGTTCCCCTTGGGTGAATGACAGTCTTT[T/A]GGACCAACAGGATGAAGGCCAATACAAGGATGGGACACGACCACTCTCATCAGACCCCAGAGACTCACCATACAGAGTGCGACCGGGGTTTTGCTCCTGATTTTACCCCTCTGAACATCTTAATGTCACTCACAAATTTAAACCCACTTGGTTTCAGACTGGGTTGCCTGGTGTCCTATTCCTGGAAAGTTCACCTTCAACCCTGATCAAACAAATGTGAAGAAGATCTTCACGAGCACTTAATGAGGGTGAATCAAGGTTGCGTCTGAACTCTGTCGGAAGATCTCGAGGATTGGGCACCCCTGACTAAGACCTTCAGGATAATGGCAGAAGTACTGGACACTCAAGTAAAAAAAAACTACTGATACCAGCCCAAGATGGTTTACTTGAAGTGGTCTTAAGCTGGTCCTAGCTGGTTTAATCCTGGTCAAGAAGGCTAAGTGGTGACTTGGTTACCTAATTGCTCAAATCCTCTCTTAAGCCAGCCAAAAGACCAGATT
Associated Phenotype:
Not determined