ZMP
map3k5
Ensembl ID:
ZFIN ID:
Description:
mitogen-activated protein kinase kinase kinase 5 [Source:RefSeq peptide;Acc:NP_001155222]
Human Orthologue:
MAP3K5
Human Description:
mitogen-activated protein kinase kinase kinase 5 [Source:HGNC Symbol;Acc:6857]
Mouse Orthologue:
Map3k5
Mouse Description:
mitogen-activated protein kinase kinase kinase 5 Gene [Source:MGI Symbol;Acc:MGI:1346876]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32269 | Nonsense | Available for shipment | Available now |
sa32268 | Essential Splice Site | Available for shipment | Available now |
sa43368 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17844 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32269
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 |
---|---|---|---|---|---|
ENSDART00000046641 | Nonsense | 684 | 1364 | 15 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 3067910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3021772 |
GRCz11 | 20 | 3034612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCATGGAGAGAAGGTGGTTCTGGGTAAGGGCACCTTTGGAGTTGTCTA[C/A]GCTGGCCGTGACCTCAGTAACCAGGTGCGCTTAGCCATCAAAGAGATACC
Long Flanking Sequence:
GTACATAGTGCATGAGTGCATAGTGTGCCATTTGGGACGCAGCTAATGAAAATATTTGATTGATCATGTATTGTTGCGTGTAGTTAGGACATGGCTTAAGCTCGGTAGTCAGGCACGTTTGCTTCTGTTAGTGTCATCAATCTGGATTTTAGTCATCGTATGAGGAGTGACCGGTGGAAAAAAAACTCTCTAGTGTTTTGATTTTGTGTTGCAATAAACACTGCAAACCATCCTAAATACTGCACCTTAATAATGCACTCAGTTTACTGTAAATCAGACTGTCTACAGTACACTAAACATATAAGTATATTTGTTGTAAATCTTTCCAGTTCAAGGAATGTTTATGGAAAATGCCTGAAATGTGTATTGTTGTGTATATTTATGTACAATGTTGAGCGACAGAGAGGATGACGTGTTTGTGTGTGTGTGCAGTATGATTATGAGTACGATGAGCATGGAGAGAAGGTGGTTCTGGGTAAGGGCACCTTTGGAGTTGTCTA[C/A]GCTGGCCGTGACCTCAGTAACCAGGTGCGCTTAGCCATCAAAGAGATACCTGAACGGGACAGCAGGTGAGCAATTACACCTTTTAAGGTTTGTCTGATGAGATCCACTTTGAAATCCCTCTCGAAAGCAATATGCTTCCTTGCAATTTATTATTATTATAATTCAGTGTTTCCTCTAGAATTTTGTGGCGGCAGGTCTTTTACACAAATCTACCAACTATGGCGTTATTTCAGTGTGGTAAGCGCAGTATTACACGTCGGGATCGCATTTATTTCATGTAAATACGAGCATGCCAATCTCTGCTTGCGCGCCGATTTTCTCTGCTCGTGCACAAAACTTCTTGCACATCCTCAAACACGCTGCTCAAGCTCAGATCTTCTTGTGCGCTCTCAAATAAGCACTGCTGAAGTGCGATTTAGTGCGATTATGTAGTGACTATGTCTCCAACATTAATTAGATTTGCTAGGAATATTTATGAATGTCTCTAATAGACCTACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32268
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 |
---|---|---|---|---|---|
ENSDART00000046641 | Essential Splice Site | 1163 | 1364 | 25 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 3049589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3003451 |
GRCz11 | 20 | 3016291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACATCATTCGAAAGGCTGTGCAGACTGCCATCGTCATATTGGTACCTG[G/A]TAAATGAAACCTTTATTTCTAAAACAATCTGGTAACTGCACATTCATACA
Long Flanking Sequence:
TTTAAAAAGCTGTGGACCAATCACAAGAGACCAAGCAGTTTGACCAATCAGAGCATGCTTTCTGAAAGGCGGGGTTTAGAAAGAAGGAGTCTTCTTCGACAGAATCAATTAGTTTAAGGCTCTTTGTACAGTGAGGGGATTTTTAATGTGTATTATGAAAAAACAAAGAACACAAAGGAAGCTGTATACTTTTAAAAAGGTACTAGAATACAAACACTTGAGTTAAATTGTAAGAAAAAATACTTTAGAAGTTCAAGTCTGTGGTATTTGGGCCTTTTTTATATATCTTGAATGTCTCCTAAAATGGATTTACATGAATCCATTGTCAAAAACCCCTAAGATTCATCATGAAAATAAAAAGTTCCATGTAGCCTAATGTTTTGTATTTCTCCAGGTGAATAAAGTCCTCCGCAACCACAACATCAAGCCACACTGGATGTTTGCCCTGGATAACATCATTCGAAAGGCTGTGCAGACTGCCATCGTCATATTGGTACCTG[G/A]TAAATGAAACCTTTATTTCTAAAACAATCTGGTAACTGCACATTCATACAGTTCCTGAAAGTGGAAATGGAAGTGCACATTGTTCATGCCTGCTCTTATTAAACACTTGATGACTGGTTGATTATTATAGTAGTCAATGACCTGTGCCACTGACATACCTGAAGTGTGCAGGAACTGTACTTGAAGGGGCTGTTCATAAAACTTGACATAAACAAACACATCACAACCGGTCTCTAACTGTATTATGACGACTTGACATTATGAAGACAACATCATTAATATTGTTATGAGGCGTTATAATTGTTGCTTGAATCTTTTTTCTGATTTGTCATTAAAATGTCTTATTAATTTGATTACTCTGTCAAATAATTTTGAAGAGAGTCATTAGTATTTAATCTAAATTCAGCTGTCGTTGAGGCTAGAAAAATATTAATGATGCTATTATAATATTCATGAAATATTTATAATAGCTTTATGACAATTATGTTGATGACAGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43368
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 |
---|---|---|---|---|---|
ENSDART00000046641 | Nonsense | 1229 | 1364 | 26 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 3048635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3002497 |
GRCz11 | 20 | 3015337 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGTGAGCACGCTTAGTTCAACAGTTTCCCACGAGTCGCAGAGCGCG[C/T]AGAGGTCTATCAGCATGGAGCTGGGTCGCATGAAGCTAGAAACCAAAAGG
Long Flanking Sequence:
TGAAATATTTATAATAGCTTTATGACAATTATGTTGATGACAGATTTATGACAAGTTTTGTTGTCTTGATAATGTTAAGCGTCATGTGAAAGACAAAACAGGTTGTGATGTACTTGTTAATGTCAAGTTGTCATAACAAACAATGTCATCTTTCCATTTAAAATTTCATAACTGACACTTAATAACAGTTGCCATAACATTTGCATTCATGTCATATCATGATCATAAAGTTTTCATGACACGTCTTAGGAACACCCCTTCAAGTAAAGTGTTACCGAACTGTTCCTTTCATGTGTTTGCCTTCAGAATTGCGTCCACACTTCACACTGGCATCAGAGAGTGACCCCGCCGAGCAGGAGGACATCGATGATGATGCAGTTCCTCAGGGAAACGCTGCACTAAAGGACATGGCACCAGCACTCGTTCATCACGACGACACTGTGGCCACGTCTGGAGTGAGCACGCTTAGTTCAACAGTTTCCCACGAGTCGCAGAGCGCG[C/T]AGAGGTCTATCAGCATGGAGCTGGGTCGCATGAAGCTAGAAACCAAAAGGCAAGTGTGTTTTATTTAGAATATATGTAATTGCAGCTGCTAGAGCGCCATCTGCTGTTTAAAAATTGTCCTAGAGCGCCGTCTGCTGTTAAAACTAGTCTAGAGCGCAATCTGCTGTTCTTAAAAACTAGCCTAGAGCGCCGTCTGCTGTTAAAAACTCTCCTAGAGCGCTGTCTGCTGTTAAAACTAGCCTAGAGTGCAGTCTGCTGTTAAAACTAGCCTAGAGTGCTGTCTGCTGTTAAAACTAGCCTAGAGTGCTGTCTGCTGTTAAAACTAGCCTAGAGTGCTGTCTGCTGTTAAAACTAGTCTAGAGCGCCATCTGCTGTTAAAACTAGCCTAGAGTGCCGTCTGCTGTTAAAACTAGCCTAGAGTGCTATCTGCTGTTAAACACTAGCCTAGAGCGCCTTCTGCTGTTAAAACTAGCCTAGAGTGCAGTCTGCTGTTAAACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17844
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 |
---|---|---|---|---|---|
ENSDART00000046641 | Nonsense | 1247 | 1364 | 27 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 3047171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 3001033 |
GRCz11 | 20 | 3013873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYATTTCGTCTGCTGTTTACATATGRCTGTGCTTRTRTGTTCTAGGTTGT[T/A]GGAGGAATTAGTAGARAAGGAGCGAGAATATCAGGCCATCCTGCAGCAGG
Long Flanking Sequence:
ACTATCCTAGAGTGCCGTCTGCTGGTAAACACTAGCCTAGAGCGCTGTCTGCTGTTAAAACTAGCCTAGAGCGCCGTCTGCTGTTAAAAACTAGCCTAGAGCGCCATCTGCTGTTAAACACTAGCCTAGAGCGCTGTCTGCTGTTAAAAACTAGCCTAGAGCGCCATCTGCTGTTAAACACTAGCCTAGAGTGCTGTCTGCTGTTAAAACTAGCCTAGAGCGCCGTCCGCTGTTAAACTCTAGCCTAGAGCACCGTCTGCTGTTAAAAACTATCCTAGAGCGCCGTCCGCTGTTAAACACTAGCCTAGAGTGTCGGCTGCTGTTAATAAACTATCCTAGAGCGACGTCTGCTGTCAAACACTATCCTAGAGCGCCGTCGGCTGTTAAACACTATCTTAGAGCGCCGTCCACAGAATCAATGCAGAATTATTCATGCGTTTCTTTTCACCAACATTTCGTCTGCTGTTTACATATGGCTGTGCTTATGTGTTCTAGGTTGT[T/A]GGAGGAATTAGTAGAAAAGGAGCGAGAATATCAGGCCATCCTGCAGCAGGTCCTAGAGGACAGAGAACAGGAGATCAAACTATTAAAGTGTCGAACCGGACCCATCGGTGAGGCTGACATTCAAATGATAAAACAGATTCTTCCTTCCATCTTGGTTTATTATTTAATTCTCCCAGTGTTCCATAGCACATGTTTCCTTATCATTGTGTGTAATACAAACTTGTTAAGCATTTGATTCTCATTGGCTAATGAGCAATATACGGTGTGGAGTTATTTTTCAGATAAATGCACCGCTAAAGTAGTTCCAGGCAGGTTTTGAGAGTTTGGGGTTTGAGTTTCACAGCGGAGGAGAAGTGCAGCGCCGTGTGTTTAAAAGTCTTCATCCATCTTTGTCCAAATATAGCAAATTTAGCAGCATACATACATGCGTCTGTTTATTATTTTCCTTTTTCTAGCACACGCCCAAACAAACCGGCATTTCACAGGGTTAATTTGAATAC
Associated Phenotype:
Not determined