ZMP
si:ch211-45c16.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAP3K13
Human Description:
mitogen-activated protein kinase kinase kinase 13 [Source:HGNC Symbol;Acc:6852]
Mouse Orthologue:
Map3k13
Mouse Description:
mitogen-activated protein kinase kinase kinase 13 Gene [Source:MGI Symbol;Acc:MGI:2444243]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44715 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13481 | Nonsense | Available for shipment | Available now |
sa17143 | Essential Splice Site | Available for shipment | Available now |
sa13787 | Essential Splice Site | Available for shipment | Available now |
sa13451 | Nonsense | Available for shipment | Available now |
sa34779 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15617 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44715
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 |
---|---|---|---|---|---|
ENSDART00000007401 | Nonsense | 65 | 981 | 1 | 14 |
ENSDART00000140771 | Nonsense | 65 | 981 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54352314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53195480 |
GRCz11 | 9 | 52734987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCAAGCGCTCCTGCCTCCTGCTCCTCCTCCTCCTCCTCCACCACCA[C/T]AGATCATCACAGATCTCGCTCCTCCAACCACGCTGCCCATGCCTCTCCAT
Long Flanking Sequence:
TGATTTGAAGTGCTTCTTTTATCCTCGTTAGTAGTGCTGCACAATTAATCGTTAAAAGATCGCGATCTCGATTCGACCCCCTTGACGATCTTAATCCAGATTCACAGATATGCCTGAGGCGTTTAGCATTTTTGGTCAACTAATGGTACTTTCACTTGAGAATGTTTTTTTTTAGTGCTCTTTCCACCACTGGAAATATCTAACATCCTTCTCCCTGTGTTCCTCCAACAGGCGTGTCATAAACCCCATCGGAAGGCATCCATAAAGCCGGCTGGCTGATTTCGGTGCGCTGAGGAGGACGTCTGCCCATGCACACGCACAGCACCATGGGAAGCTCCCCGGAGGTGCTGTCCTGGACGTCCTGTCCCAGCCTGCTGGTGGGCAAACTGAAGGAGGAGCTCAAACTCACAGTCGTCGGAGACTCGATAAAGAAACCCAACAATAACATCTCTCCTCAAGCGCTCCTGCCTCCTGCTCCTCCTCCTCCTCCTCCACCACCA[C/T]AGATCATCACAGATCTCGCTCCTCCAACCACGCTGCCCATGCCTCTCCATCACTTACAGCTGCCGGTTCGAGATGAGGAGCCAGGCGGCACCAGTCCTCCATGCACAGCACTTAGCGAGGACTCAACACGCGAACAAGGACACTTCGAAAACAGCGTTTTACAGCTACAGGAGCAGGAGGATGCTGAAACACCTGGATCTTGCGGTCAGGGTGGATGCGGAAGTGGCGGAGAGGAGAAAAACGAGGAGAACGGCTGTCCCATGGAGCATAGTGGAGACGACACACACCATCATCCACATGATGACATCAAACTGCACTTTCACAGAGCCGGGACGGGCAGCGGAGGGTTTCTTGAGGGACTATTTGGGTGCTTGAGGCCTGTGTGGAATATCATTGGGAAGACATATTCAACCGAGTATAAGCTTCAACAGCAAGGTTAGTGGAGTCTGGGAAGTGCCAGATTAAGTATAAATTACTAAATGAAGTCGGGTTATCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13481
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007401 | Nonsense | 208 | 981 | 1 | 14 |
ENSDART00000140771 | Nonsense | 208 | 981 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54351885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53195051 |
GRCz11 | 9 | 52734558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGTGGAATATCATTGGGAAGACATATTCAACCGAGTAYAAGCTTCAA[C/T]AGCAAGGTTAGTGGAGTCTGGGAAGTGCCAGATTAAKTATAMATTACTAA
Long Flanking Sequence:
AGAAACCCAACAATAACATCTCTCCTCAAGCGCTCCTGCCTCCTGCTCCTCCTCCTCCTCCTCCACCACCACAGATCATCACAGATCTCGCTCCTCCAACCACGCTGCCCATGCCTCTCCATCACTTACAGCTGCCGGTTCGAGATGAGGAGCCAGGCGGCACCAGTCCTCCATGCACAGCACTTAGCGAGGACTCAACACGCGAACAAGGACACTTCGAAAACAGCGTTTTACAGCTACAGGAGCAGGAGGATGCTGAAACACCTGGATCTTGCGGTCAGGGTGGATGCGGAAGTGGCGGAGAGGAGAAAAACGAGGAGAACGGCTGTCCCATGGAGCATAGTGGAGACGACACACACCATCATCCACATGATGACATCAAACTGCACTTTCACAGAGCCGGGACGGGCAGCGGAGGGTTTCTTGAGGGACTATTTGGGTGCTTGAGGCCTGTGTGGAATATCATTGGGAAGACATATTCAACCGAGTATAAGCTTCAA[C/T]AGCAAGGTTAGTGGAGTCTGGGAAGTGCCAGATTAAGTATAAATTACTAAATGAAGTCGGGTTATCTTTATTAATAGGGGTGTCACCATTTCGATTTTTAATCGAAATCGATCGAAATTTATGCTCAATTTCGATTATCGAATCAAAAAAAAAGAATCGTCGATGCTGCCACGCCCCCATGTCACGTCAGCTTGTCTTGCCAAGCGGGAAAAAAACAGGCTTGTTAACGTGCTTGTTGAACTGCAGATATAGGAGACCCGTCGACAAAGCTTAAACCCTCTCCTCTTTCAATGAAGTCGCCGGTGTGTAAGCATTTTGGATTTCCAGTGAGTTATGTTGACAACGTTCGTGTTGTCGACAAAAAAAACACAAGCTCTGCTATGTACGTATTAGGGTTCGTCCGATAGACAACACCGACGCCATTATTTTTTACCGACGCCATTATAACGACACAGATCACTGCCTATTCACGAGTCCCGCAGAAAAAGTGATTGACAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17143
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 |
---|---|---|---|---|---|
ENSDART00000007401 | Essential Splice Site | 388 | 981 | 4 | 14 |
ENSDART00000140771 | Essential Splice Site | 388 | 981 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54340378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53183544 |
GRCz11 | 9 | 52723051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTGAAGTCATCCGGAATGAGCCGGTGTCTGAGAAAGTAGACATCTGG[T/C]GAGTGTGGATTAATGCRGSRTCATTCAGTGAGATTTAAGTGTCTGGAKWC
Long Flanking Sequence:
ACTGGGCTTCAGGAATCGCCAGCGGCATGAACTACCTGCACCTCCACAAGATCATCCACAGAGACCTCAAGTCACCAAAGTACGGGTGCTTTCATACCTATAGGTTGTTTGCAATCATGTGGCATGAAATTCAAGGGACAAATCTTTAAAATATGTCAGTGTCATTGTTTCTGCCTCAAGATGCACACTATTATTGTGTTTTTTAAGTCAGTTTTGATGCTTAAAACCGTAATTCCACCAAGGCCTATTCCTGGCACACATAACTTAAAAAGCAACTATTAACAATCTTTTTAATTATTAAAATGTGTACTCTTATAAATGGCGTTGTTTTCTCTTGCAGTGTGCTAGTCACTCAAAATGACAGTGTGAAGATCTCGGACTTCGGCACATCTAAAGAGCTCAGTGATAAGAGCACCAAGATGTCGTTTGCGGGTACGGTGGCCTGGATGGCTCCTGAAGTCATCCGGAATGAGCCGGTGTCTGAGAAAGTAGACATCTGG[T/C]GAGTGTGGATTAATGCAGCGTCATTCAGTGAGATTTAAGTGTCTGGATTCCAAAATGCATTAGAATGTGTTGCTTTTATAAAAAAAAAAATTTAGATTTTAAGCATTTTTACCTTATATTATGGACAGTGGTGTAAAGTAACTAATCACAAATACTCAAATTACTTTAATTGAGTAGTTTTCCTCAAAAATTGTAATTTACTAAATGTGTAAATTAATAAATGTGTACTTTTACTCTTCCTTGAGTACATTTTTACTGCAGTATTGATAATTTTACTTCACTACTTTTAGAGTTAGAGCCGGGATTCAAATCATATATATTTTTTATATTTTATATATAATAAAACATATTTTTATTCTATTATATTTTATTATAATTTAATATATTATATTATATTATTTTATATTATTGTTACATTCTATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATATTTTATTATATTATATTATATTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13787
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 |
---|---|---|---|---|---|
ENSDART00000007401 | Essential Splice Site | 477 | 981 | 6 | 14 |
ENSDART00000140771 | Essential Splice Site | 477 | 981 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54336056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53179222 |
GRCz11 | 9 | 52718729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCCGCTGATGTGCTTGGGACGCCACAGGAGACCTACTTCAAATGYCAG[G/A]TCAGAAAAACACANNNNNNNNNNNNTGAGATTCATYTGCAAACCACTCTT
Long Flanking Sequence:
AAGAGCAGGGGTGTAACCCCGGTGTCCTGGCCAAAGTCCCTCTATCGGCCCTTACGATTATGGCCTCTTAATCATCCCCTTCCACCAAATTGGCTCTATCACTGTCTCTCCACTCCACCAATAGCTGGTGTGTGGTGAGCGCACTGGCGCCGTTGTCCTGTGGCTGCCGTCGCATCATCCAAGTGGATGCTTCACACTGGTGGTGGTGTGGAGAGACCCCCCTCATGATTGTGAAGCGCTTTGGGTGTATGGCCATACACAATAAATGCGCTATATAAATTTACATTACATTACATTATACTATGTCCTAAAAGTACTGTATGTTTGCAGCTCTGTTCTGAAAGAAAGTAATATGGCTTGTTTGTGATTAGTATTATTATATTTCCTGTAGGCAAGGCAAACCTAGAAACCGGCCGTCTTTCAGGCAGATCCTCCTGCATTTGGATATCGCCTCCGCTGATGTGCTTGGGACGCCACAGGAGACCTACTTCAAATGCCAG[G/A]TCAGAAAAACACACGCGAGTCATCATGAGATTCATTTGCAAACCACTCTTGAGTCGATTCAAAATTGCTTCCAAATCTTTCTTACATTTCTGAGTTACTTGTTTTGTTGTTACAAAGCACCTAAAAGAGTTGAGGAACAGAACCATTAAGGAACTTTTGGAATTTTAGATTTTTAACTAATTTAGTGATCCCTTTAAATCAGTGTTTGGCTGCAGACTTGCACCTCCAGGCTTGCACGCCCACGCAACCGCACTCCCTCTGCAAGTGACGTCATTTACAATCGCCACCCGTGTCCGCTTGCATGAAAGTCCTTCGGTAATTTAACTTAAGGGTGTCCCTGAGGCGGAAAAATCTCTGAGGTAACGGATTTCATTAAGATCTTTGCAACAAACTTCTTATCCGTCACCCTGACCAAAGAACATAGAATCACCAAGAGGCGACACTCTAGTGCAGTTTGGGAAATAGCCACTAGATGGCGCGGCGGCCATTTTGGAATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13451
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007401 | Nonsense | 489 | 981 | 7 | 14 |
ENSDART00000140771 | Nonsense | 489 | 981 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54333186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53176352 |
GRCz11 | 9 | 52715859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAATAATCTGTGACAGACGGAGTGGMGAGAGGAGGTGAAGAAAYATTTC[G/T]AGAAGATCAAGAGTGAAGGCACATGCATCCATCGGCKGGACGAGGAGCTG
Long Flanking Sequence:
ATTATATACATTTGTATTATTTATCTGGTGTATTTTTACTTTCTTTAATTTCACTATTAATTATTAAAATAACTATATTTTCAGTTAGTTGCAGTTGTAGGTTTTACATCTAATATTTGCACTTTGCATTTTAGTTACTGAGCTTTTTTTAGCAGTTTGATTTTTATAATATCCACACTGTATTTAAAATATATTACATAGTTATACTATTGCTCAAGCCCCTTTTTTGATTTAGTTCTGTTCTGTTTTGTTCTTTGGTTTTGATTTAAATTTATTTATTAAAAAAGGAAAACGTTGAAATGTCTGGTTAAACATTATATTCGCCATCTCAGTCTCTAGTATAGATAAATAGCAGGTCGTATACAGCCACTGACTTGGGTTTGTTTTGTGGCCTATTGTTCTGCTTCTCAAACAACTTCTTGGCTAATGAATAATTAAATGAACAACAAAATAATAATCTGTGACAGACGGAGTGGCGAGAGGAGGTGAAGAAACATTTC[G/T]AGAAGATCAAGAGTGAAGGCACATGCATCCATCGGCTGGACGAGGAGCTGATCCGCCGCAGAAGAGACGAGCTCAGGTATATATTAACTTCAATTAATTCATTTAATATATTTATTATTGTATTTTTTTATTTAGTTTTTGTATATATTTTTGTTTAATGAATTCTTATGATTTTATTGAACTCATGCCTGTGGTTTATAAATAAACTTTGACAGTAAGAGCTCATGCTGTGTGTGTTTCTCACTGCCTCTGTGTGCTTCAGACACGCTCTGGACATCCGAGAGCACTATGAGAGGAAACTGGAGCGGGCCAATAATCTGTACATGGAGCTCAGCGCTATCATGCTACAGCTGGAGGTGCGCGAGAAAGAGCTGCTCAAGTGAGTTCCTCAAGCTTTTCAATTATTCATTGCAGTAAGTAGAGGTTTCGTGCTAAAAAATAAGGTGTGTTTTCAGTAAACGAACACAAGGGGCAATCATATTGCATCAGTTTTTCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34779
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 |
---|---|---|---|---|---|
ENSDART00000007401 | Nonsense | 543 | 981 | 8 | 14 |
ENSDART00000140771 | Nonsense | 543 | 981 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54332838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53176004 |
GRCz11 | 9 | 52715511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGGAGCGGGCCAATAATCTGTACATGGAGCTCAGCGCTATCATGCTA[C/T]AGCTGGAGGTGCGCGAGAAAGAGCTGCTCAAGTGAGTTCCTCAAGCTTTT
Long Flanking Sequence:
ATAGCAGGTCGTATACAGCCACTGACTTGGGTTTGTTTTGTGGCCTATTGTTCTGCTTCTCAAACAACTTCTTGGCTAATGAATAATTAAATGAACAACAAAATAATAATCTGTGACAGACGGAGTGGCGAGAGGAGGTGAAGAAACATTTCGAGAAGATCAAGAGTGAAGGCACATGCATCCATCGGCTGGACGAGGAGCTGATCCGCCGCAGAAGAGACGAGCTCAGGTATATATTAACTTCAATTAATTCATTTAATATATTTATTATTGTATTTTTTTATTTAGTTTTTGTATATATTTTTGTTTAATGAATTCTTATGATTTTATTGAACTCATGCCTGTGGTTTATAAATAAACTTTGACAGTAAGAGCTCATGCTGTGTGTGTTTCTCACTGCCTCTGTGTGCTTCAGACACGCTCTGGACATCCGAGAGCACTATGAGAGGAAACTGGAGCGGGCCAATAATCTGTACATGGAGCTCAGCGCTATCATGCTA[C/T]AGCTGGAGGTGCGCGAGAAAGAGCTGCTCAAGTGAGTTCCTCAAGCTTTTCAATTATTCATTGCAGTAAGTAGAGGTTTCGTGCTAAAAAATAAGGTGTGTTTTCAGTAAACGAACACAAGGGGCAATCATATTGCATCAGTTTTTCTTTATACATTTGAAGTCAGAATTATTAGCTCCCCTTTTAATTTTTTTTTCTTTTCTAAATATTTCTCAAATGATGTTTAGCAGAGCAAGGGAATTATCACAGTGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTAAAATAAAAGCATTTTTTAAAATTTTTTAAACACCATTTTAAGGTCAATATTATTAGCCCCTTTAAGCTTTACTTTTTCCCGATAGTCTACAGAACAAACCATCATTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCAATTTCAGCTGTGTACTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15617
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 |
---|---|---|---|---|---|
ENSDART00000007401 | Nonsense | 562 | 981 | 9 | 14 |
ENSDART00000140771 | Nonsense | 562 | 981 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 9 (position 54328824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53171990 |
GRCz11 | 9 | 52711497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTTACATGTGTTTTCTGCAGGAGGGAGCAGGCCGTGGAGAAGAAGTA[T/A]CCGGGAACGTACAAACGCCACTTGGTTCGGCCCATTGTGCGACCCAATGC
Long Flanking Sequence:
CATCATACTGCCCCCTAGTGTTTATTTACCTTAAAGCTCCCATTAAATGTATGTTAAACTACTTTTTTTGCGGTTTCACATAAAACGTAGGCTGAAGCACGTATTTTCAATGAGCCTGTTTTGTTTATAGTGAATGTACACTACAGATGAAGTGCGTATTGTATAGTAGTTATATTGTAATATGCAATTGTGAACATGCATGTTAATTTGTGTGTCTCTCTCTCTTCAATCTGTTTGTTTATTAGCATGAAATTGCAGTAATGAGTCTGAACTCTGACCTGTCAGTGCCTGAGTGCTGACATCTCCCTCAAACTCTCATTAAATCTAATCTGCTTTAAGCTTGTCTTGACTCTGCAGAATATTACTGACCCTTATTTTCTCTGAATTAGCACACAGTGATCATCCCGTCAGATCGTGCACACATCTGCATGTCTGCTTCAGTGGTTTGACAGTTTTACATGTGTTTTCTGCAGGAGGGAGCAGGCCGTGGAGAAGAAGTA[T/A]CCGGGAACGTACAAACGCCACTTGGTTCGGCCCATTGTGCGACCCAATGCTGTTGAGAAGCTCATAAAGAAGAAAAGCAGCATGAACCACAAACCTGGGACGCAGCAGCCTAAGAGGTGAGATATCTGCAGGGTTCATGCAGTCATTTGAAAAACAGAAAAACCCACATGGTTTTGGATAAGTTATGGCAATTAGTTTAACGAATATCTGTATAGTTGAATATAGGTTAGTTGTCTTTAATTCTTTTCTGTCCTTGGCTAAAAACATTACTCTCACATTATTAGTGCAGTGTAAGCATTATCTAAATCAATTTTATATAGATATTAAAATAAGTTTAAACTAAATAGATTGTTGCGTGTAAATGCATGTAGACTGCATGCTGTAATAGATTTGAACATGCATGGTTTTACATAGATATTAAGGGCTCTATTTTGACGGTCCATGCGCAAAGCGCAAAACACAGGGTGCAAATGCTTTCAGGGCGTGTCAGGACGCGTTTT
Associated Phenotype:
Not determined