ZMP
map3k7
Ensembl ID:
ZFIN ID:
Description:
mitogen-activated protein kinase kinase kinase 7 [Source:RefSeq peptide;Acc:NP_001018586]
Human Orthologue:
MAP3K7
Human Description:
mitogen-activated protein kinase kinase kinase 7 [Source:HGNC Symbol;Acc:6859]
Mouse Orthologue:
Map3k7
Mouse Description:
mitogen-activated protein kinase kinase kinase 7 Gene [Source:MGI Symbol;Acc:MGI:1346877]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa230 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa23699 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa230
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000018545 | Nonsense | 22 | 562 | 1 | 19 |
ENSDART00000025862 | Nonsense | 22 | 551 | 1 | 16 |
ENSDART00000124919 | None | None | 211 | None | 6 |
ENSDART00000130414 | Nonsense | 27 | 602 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 24164723)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24283524 |
GRCz11 | 20 | 24182624 |
KASP Assay ID:
554-0128.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGATATGCTGGAAACACCGCCTATGTATCCGTTTGAGGAGATCGATTA[T/A]GTTGATATTGAAGTGGAAGAGGTGAGTGATTTCATATGCGTTCTGTTTAA
Long Flanking Sequence:
GCGCTGCGCGGACAGGAGATCCAGCGACCGCACCAGCGCGAACCAGAGAGCGGCCTAGGGCTAACACTCACAAACGGCGCATTTATGTCGACGGGACATCCATAAGTGTACTTGACAGAGATCCTAGGATCTACTTCCTTCTGAGCGACAACGTTTTTCGTCGTTTGACATGCCCGGCATACTTTAATCTGCACCGGAGCCTCTTAGCATCTTTGCTAACGGATTAGAATTGACAGGTTAGCTTGTTAGCCGCTAAACACGTTTTAAAGTGACTTCTCGCACACGTAAATCTATGTAATGAAGTCAGTGTCGAGGGAAGAGGCACTCCAGCTCTCATTTTTATTCTGAAACCACTCGTTTGTGAATTTTGGATAGTTTTAAGACTATACAGTCTGTTGTTTGTGTTTTAATGATTAGCTGGCTAGCGAGCTAGCGATGTCTATGCCCTCCGCCGATATGCTGGAAACACCGCCTATGTATCCGTTTGAGGAGATCGATTA[T/A]GTTGATATTGAAGTGGAAGAGGTGAGTGATTTCATATGCGTTCTGTTTAATTAATAGTCGTGCTGACAGGAGTGTGGAAATGTCTTGCAAACAGTCCCTAAATGGATGCAGAATGAGATGCATGACATTGTATCTCAGCACACCTAATCTCTATTTTTAACCTTATTTGTAATATTTTATGTTTTTTTGCATTTAAAAATGTATTAGTGTCCTATGCTCACTGAAGTTTTCAGTTCGTTTCATGAAACATTACTGTTACACTGTTCTAGATTTGAGTTTGATGTGTGAGGTTTGTTTTGAACTGCCCTGCACTGCTGTCAGGTTGTGAATTGTACTTGATGTGATTTTTCTCCACCGTGTGTTTTGTAGGTGGTTGGCAGAGGGGCATTTGGTGTTGTCTGCAAGGCCAAGTGGAAAGGCAGAGATGTGGCCATCAAGACTATAGAGAGTGAATCTGAAAAAAATGCTTTCATTGTTGAGGTATTGCCACATCCTATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23699
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 |
---|---|---|---|---|---|
ENSDART00000018545 | Nonsense | 355 | 562 | 13 | 19 |
ENSDART00000025862 | Nonsense | 371 | 551 | 11 | 16 |
ENSDART00000124919 | None | None | 211 | None | 6 |
ENSDART00000130414 | Nonsense | 377 | 602 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 24149218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24268019 |
GRCz11 | 20 | 24167119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAGAGTCTTCCTGGCAGGTCACATTTTCAGCCTTCCTCTGACAGCAAA[C/T]GAATGAGTGTCGAACTCTCCGAATTGGAGCCCAGATTACCCTTTGCTTCT
Long Flanking Sequence:
TGGGCGTTGACAGCATGATGAAATATTTCAAAATTTTATCTTTTAAACATGCGTAAATACAACGTTGATGAGCATCAGAGACTTTTTTACGAAAACGTAAAAAATTTTAACTACCTCAAACATCAGAACAGCAATGGTATAAGTCAATTTTGGATTGTTTAAAAATGTATTGAAGTCTCTGGTAAAGTTGTCAAGTTTAATGTAATATCTCTCAATTGTAGGCTCACATTTAGACTACACATGTACCAGCAATAAGAACGACATCAACATGGAGCACACAAACTCCCCTGGCAGTAACGATACAATCAAGTTCCCCTACAAACCAAAGGTAATTCATTAACCGTCCACATAACCGCACAAAGACTGAGATACAAAGAAGCTCATGTTTGGAACTTGTGTTTTTGTGCATTCAGGGCATTTCTGGTCAGTCTCTCTCCAGAGGCAGCAGCGTAGAGAGTCTTCCTGGCAGGTCACATTTTCAGCCTTCCTCTGACAGCAAA[C/T]GAATGAGTGTCGAACTCTCCGAATTGGAGCCCAGATTACCCTTTGCTTCTCCAGGTAACTTATGCTGCTTCCATGCTTGTCATAAAGTTTCAGACCTACCCAGAACCTCACAGACAATGACATTTCACAAATCATACCCTTAAATTAAATTGTTCTATAGAGCCCTGTGAACTATCTTTCATTCATTTCCAGATGACATTTTGATGGTTTAGGTTTAATTCATCCAAAAAGTAGTTTATTATAATCATGAAGGTTACAATTTTGCAAACATACTATTTTGCAATTTACAGAATTACATTTTTAGAAGTTATAAAAATTTATTTAATTCCTGTTCAAATTAAAAGATGGAAAATAATGGTCTGATTATTTATAAGAGCATTAAGCTGCTATGATTGAAATTTATGTATTGAATTTTTATTATTAATTATGCCAAATATTATTAATAGTATTAATAGCCTATAGGGTTGGGCGATGTCGAGCAATTTGGTATCGTGTGATGT
Associated Phenotype:
Not determined