ZMP
map3k4
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to H.sapiens MAP3K4, mitogen-activated protein kinase kinase kinase 4 (MAP3K4)
Human Orthologue:
MAP3K4
Human Description:
mitogen-activated protein kinase kinase kinase 4 [Source:HGNC Symbol;Acc:6856]
Mouse Orthologue:
Map3k4
Mouse Description:
mitogen-activated protein kinase kinase kinase 4 Gene [Source:MGI Symbol;Acc:MGI:1346875]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1374 | Nonsense | Available for shipment | Available now |
sa11281 | Nonsense | Available for shipment | Available now |
sa22347 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1374
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 |
---|---|---|---|---|---|
ENSDART00000075333 | Nonsense | 196 | 1488 | 3 | 30 |
ENSDART00000137256 | Nonsense | 230 | 770 | 3 | 8 |
The following transcripts of ENSDARG00000053303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 36226524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35699090 |
GRCz11 | 13 | 35824922 |
KASP Assay ID:
554-1286.1 (used for ordering genotyping assays)
KASP Sequence:
ACGCTCGCCGTAGTGTTAATGACCAGGACCTGTACCTGTTYACCGCTCGA[C/T]AACACATACCTGACATYATCAGCGAGGTTTTGCACTTCAAAGTGGACTAC
Long Flanking Sequence:
TTTCACCAACAGAGAAGTCGTGTTCATCCAGCCCCTTGTCTCAGCGTGAGCGTGAGGGAGCCAGATCAGCCGAACCTCCTGAAGAGCACAGCTACAAGCAGGAAAAGAAGCAGCGCTTCAACCAGCGATCCAGCGAGCGGGACGTCAAGAAGAAGTTTGAAGGCGCCTTTATGCTGGATCCTGTTTCCAAGTCCAGTACCATCGGCTCCAGAAACATGGATCCCCGCAAGCCCTACCTGAGTCTGGGCATGATCCCCGTTCGCACCCATCGGCAAACTTCGCGCACAGACTGTCCTGCAGACCGCCTTAAGTTCTTCGAGACCCTGCGGTTGCTGCTTAAACTCACCTCCATGTCATCCAAGAAGAAGGAGAAGGAGCAGCGAGGTCTGGAGAACACCGCTTATATGGAGCAGAACAACGAGGTCATCTGGCTGGAGCTGCAGGCCTGGCACGCTCGCCGTAGTGTTAATGACCAGGACCTGTACCTGTTCACCGCTCGA[C/T]AACACATACCTGACATCATCAGCGAGGTTTTGCACTTCAAAGTGGACTACAGTAGCCTGTGTGGACTCGAGAGTGGCGCCTCTGTTGAGGAGAGCAACTCCTGTCCTGGTGAAACTAATTGCATGGACGATCCATTTAGCTTTAGCACATGTTCCGCGTCCTGGCAGGAAATTGATGCCGCTGCTCCTTTTTCTTCAGGGCTGGAGTGCCGCAACCACCTGCAAAGGCAGCGAGTAGCTTTCGATCAGGTAAAACGGGTCATGTCGCTGTTAGAGTCGGTGGAGGCTTTGTACCCTTCTCTGCAAACCTTGCAGAAGGACTATGAGAAGTATGCAGCTCGGGACTTCCAGGGCAGGGTGCAGGCGCTCTGCTTATGGCTCAACATCACTCAGGACCTGAACCAGAAACTGCGCGTGATGGGCACCGTGCTGGGCCTCAGGGACCTTTCCCGCATCGGCTGGCCCATCTTTGAGATTCCATCACCTCGCTGCTCTCGAGGC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa11281
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 |
---|---|---|---|---|---|
ENSDART00000075333 | Nonsense | 599 | 1488 | 7 | 30 |
ENSDART00000137256 | Nonsense | 659 | 770 | 6 | 8 |
The following transcripts of ENSDARG00000053303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 36219921)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35692487 |
GRCz11 | 13 | 35818319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTCACRCAGGTGTACTTTGACTACATGCGCAGCTGGATCCAGATGTTA[C/T]AGCAGCTTYCTCAAGCRTCCCACAGCCTGAAGAACCTGCTGGAGGAGGAA
Long Flanking Sequence:
TCACTAAACTGAACTTCAACTCTGAAAACTGGACTGACACAGTTTCAATATACTAGAACTTCCATGTTAAGCTGATTTAACACAATCTACATTGTAAAACACATAGAAATAAAGATGAATATTCAATTCATGAATATTCACAAATTATGACATTGCTTACTATAAGATTGTTACAGTGTATTTGTGACTCAGTGGGTGCTTTGTGTTTCACTGCCAAGATATTTTTATTTGCCCAGCTGTGTGCTTTTTAACGTTTAGTTTTTTTTTTTTTGCATGCGAGTAATTAGAGAAAATAACTTCTGATGAAATATTAGCGATCAAAGTTTTAAGCAAATCTGTAAAAATAAGATTTATACTTCAGCTGTAAAAGCAGTTGGACAAATCCCGGTATTTCTCCCTCACGAACAGCAGTGATCTGAATAGACAGACAGTAAATCTTCGGTGTGTCTGTGTTCACACAGGTGTACTTTGACTACATGCGCAGCTGGATCCAGATGTTA[C/T]AGCAGCTTCCTCAAGCATCCCACAGCCTGAAGAACCTGCTGGAGGAGGAATGGAACTTTACCAAAGTCATCACTCCATACATCCGAGGCGGAGAAGCCCAGTCTGGGAAGCTCTTCTGGTTGGTATTTTCAATCTGTGCGCTTGCTGTATAAAGGACAAATGACAAATAAATGTTGAAGTATTATACAATGTATTTGGTTTCTGTTCTACTAGAGGAATTACAGACATAAATTCAAAAAAAAAAAAAAAAAAAAACTGTTTAGAGTCAACATACTCCTTCATATAATAATTCACTATTTAAAATGGGACTTGACAGCAAGTAGCTAGAATGTATGAAGAAGATTTTTAGCTTGCCTATTGAGGAGAAACTTCACAAATTTGCTGCCCAAATATTTTTGTTGAAACTCATTTTTTTTTTTGTCTATTGTGTGTCTATGGGTATTTGGGCAATTTTGGGAATTTATTAAGGCAAGGATGTTCAAACTTGGTTCTGGAGGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22347
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 |
---|---|---|---|---|---|
ENSDART00000075333 | Nonsense | 1224 | 1488 | 23 | 30 |
ENSDART00000137256 | None | None | 770 | None | 8 |
The following transcripts of ENSDARG00000053303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 36202868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35675544 |
GRCz11 | 13 | 35801376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACGATAACGTGATGCATGTGGGCCTGCGCAAAGTCACCTTTAAATGG[C/T]AGAGAGGAAACAAGATCGGTGAGTGAACAGCAGTGTGCATATGACGAAAC
Long Flanking Sequence:
ATAATTATCCAAAAATGTAATTGTCAAATAAATAAATATTTTAATTTGTAATAGTTTTACATTATTAATGCCTTGACTGTATTTTTGTTAAATTATTGCAGCCTTGCTATAAGCAGAAGATACTTTTAAATATTCCACATTATGAACTTTAAACTTTGACATGTTTTATAAAAAAAAATCATACTCAACCCTGAGACTGCAGTGACTAAACAGATGTTTCAATTGTTTTTAATGGATTCACATAAATGCACTGTTTTCTGAATCTGTTTTATTTATATTAAAATGTGCGTAATCTCTGAAATGGATCTTCTGCTCTTGTTTGTCCTGCAGACACAGCGCGTCAGAGCCCCCTGGAGGCAGTGCGGCGCTCCATACAAACCTTCGATGAGAAACACTATGCGCTTATGAGACAGAGAAACATCATTGGACAGGTTTGCAACACGCCGAAGTCCTACGATAACGTGATGCATGTGGGCCTGCGCAAAGTCACCTTTAAATGG[C/T]AGAGAGGAAACAAGATCGGTGAGTGAACAGCAGTGTGCATATGACGAAACGCCGCACAGGCTAGTTTCCTGAACACTGTTTCTGGCTGACAGGTGAAGGGCAGTATGGGAAGGTTTACACATGCATCAATGTGGACACTGGTGAACTAATGGCCATGAAGGAGGTATGTAAAGTATCAGCTATATAAACGTGTATAATTATTTATATTTTACAGTAACATTATTAATTTGTTATTAGCATTAGCTTAGCTAACACAAACCAGTAATGAGAATCTGGCATTTGTTAACCTTTTGTTAATGTTAGTAAATGAAAATGTTCAAATGTTGAGATTAATGTTAAGATAATCAATGCTACTGTCTAGAAGTATTGCCTACTGTTAGTTCTTGTTAATTAATTTGAACTGTAAATTGAAACCATTTTAGCTTTTTACACTTGAAGAGTTCAGATGCAGAAGCTGTTAAACGCCACTTCCGCCAAAAATGAGATAATGACATTGAGTA
Associated Phenotype:
Not determined