ZMP
Q1LYC1_DANRE
Ensembl ID:
Description:
Novel protein similar to vertebrate mitogen-activated protein kinase kinase kinase kinase 3 (MAP4K3)
Human Orthologue:
MAP4K3
Human Description:
mitogen-activated protein kinase kinase kinase kinase 3 [Source:HGNC Symbol;Acc:6865]
Mouse Orthologue:
Map4k3
Mouse Description:
mitogen-activated protein kinase kinase kinase kinase 3 Gene [Source:MGI Symbol;Acc:MGI:2154405]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12892 | Nonsense | Available for shipment | Available now |
sa36410 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45607 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36411 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18499 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12892
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 |
---|---|---|---|---|---|
ENSDART00000093004 | Nonsense | 3 | 864 | 1 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 24460604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24614046 |
GRCz11 | 17 | 24632447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAACGTAAATAAACCGGAGGGCGCAAACGGTGACTCGCACGATGAATT[T/A]AAGCTTGGATCTATCGCGCAGAAACCCACAGGAGGACTTTGAGCTGATCC
Long Flanking Sequence:
CGTTTTGAAAAAAATAAGTATTAAAGTTAATATGTAATTAGTTTAAGGTAATTATGTCAGCTTAATTATTAGTTAACAACCATGTTCTGCCTAAGTTATGTGTCCCCTGAATAATAACTGCCTATATTTATTATAATTTAGAAGCTGTTTTGTTTTAAACAAGTTTTGTTTAAAACGATTAGTTCGTGTTGTCTTTCTTTATTGAAATGAAGTGATTTTATATGTATTAAAGTGAAATAGATCCATTATCAGCGTTTCTGAAGTTTCCCGGTGTCTTTCTGCTTCATTATGTACACATTTCTCTCCATCCTCGGTACGTGTTGTCAGTCAGTCGTACTGCGCATGCGCAGAGGAGGCCATGTTGTTGTAGTTCGGTGGGACTGGACCGTCATATCCCATCGTTACTGTATGTCTGTGCGATCATCACCCCCCTCCCGTTTTTGACATCGGGAAAACGTAAATAAACCGGAGGGCGCAAACGGTGACTCGCACGATGAATT[T/A]AAGCTTGGATCTATCGCGCAGAAACCCACAGGAGGACTTTGAGCTGATCCAGAGGATCGGGAGCGGAACCTATGGGGATGTATACAAGGTAGAGATCAACTGGGTATCAGAACCTAGCAAGCTACCTACCTAGACTGCATATTTGTACACCATAGGCGCTTTTTTCAAAAGGAGAGAATGCGCCTGTGGTGCCCGAAAACGCTGTCTTCTTAGGGAGCTCACTAGGGATTAAGACACAGCCACTTAACTGACCAATGAACCAGTGTGTACGAGAGACAACAGATGTGTGTTTACACCGGACCGCAGTGTATTTGTGTTCTGTAGCAATTTTGCGGCTAGGATGTGGTGTAATATCCTGAAAGACTCTGAAGATCTTTGTTTGCATAATGCACACGGCCTAGCAAGTCTATTTCATTAGAGAAAGCCAGTGCTAAGCTGTCAGATTCACATCTTCCATCTTTTTATGTGATGTACGTGACATAAACAAAGACAAGAGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36410
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093004 | Essential Splice Site | 153 | 864 | 7 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 24468971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24622413 |
GRCz11 | 17 | 24640814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGGGTGCAAATATACTGTTAACAGACAACGGCTATGTTAAGCTAGG[T/A]AACAAAACACATTTATTGGAGATCACAGTTATTCAGAAGCACTAACCTTT
Long Flanking Sequence:
CATAATTAGCACTCATGAGAATGGAGAAGAGGATGTTGTTCTTAAAATAGAAATATCAATGAATAGATATTTTAACCGGACAATTTCATTAGATTTAATCTTGTAATCACAAATATTTGCACAAGACCAAAACATCCTGAATGCCTGTGGAATAAATGTGATTGTTCTTAAGTGTCTGTGCATGAATACACTGAGCGATCATTGTATTGACAACAAAAATACATGGTTTGTTTGTGCATCAAAGGGACTTAAACGTACTTATTTTACGACTTCTGTTTGTCACTGTAACCTTGAATACAATTCTCATCTTTCAAAGCTTTACTAGCAAGACCTTTAAGTTTTCTTTATCCAGCTCAGATGTCAGTCTGAATCAAATATTATGTCTCATCAGAAATGTAGATTTAAAGAGTTTGCTCATTTACAGCTGCTCATATTGGTTCTACTCTTGTTTTGCAGGGTGCAAATATACTGTTAACAGACAACGGCTATGTTAAGCTAGG[T/A]AACAAAACACATTTATTGGAGATCACAGTTATTCAGAAGCACTAACCTTTCCTTTCTAACATCTTTCGTCTGTCTCTGTCCAGCTGATTTTGGCGTTTCGGCTCAGATTTCAGCCACTTTAGCAAAAAGAAAGTCCTTCATTGGAACTCCATATTGGTATGCCAGTCCTTTCTCATTCTAATAGTTTTCTTCTAGTTGTTAAATTGCAAAAATTAATTTCTCTACACTGTGTGTGTTTCTCTGCAGGATGGCACCTGAAGTGGCAGCAGTGGAGCGGAAAGGTGGCTATAATCAGCTGTGTGATATTTGGGCTGTGGGCATCACAGCTATTGAGCTGGCGGAGTTGGAGCCACCAATGTTCGACTTGCACCCTATGAGGTGTGTTTCCAGTGACTTGGACTGATTTAAAGTCTCTCTGCTAAATTTTGTGCTAAATTAATTGACTAATTCCATAGTTTAAAGATATTATAGGCCATGTTTTATGTGACAGGGCTGCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45607
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 |
---|---|---|---|---|---|
ENSDART00000093004 | Nonsense | 593 | 864 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 24484658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24638100 |
GRCz11 | 17 | 24656501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGAAACTCTATACACTTCTATGTGTGTGTTTCACAGGTAAAGCATCT[C/T]AGCTGTACTCCTACAACCTGACGGGGCTCTTTGAACAAGCGCGACAGATG
Long Flanking Sequence:
TGTATGAGAGTGTGTGAACAAGTGTGTATGGATGTAAAACATATGCTGGATAAGTTGGCAGTTCATTGCTATGGTGACCCCTAAATAAAGGGACTAAGCTGATGGAAAATAGATGAATGAATGATATCAAAATAAGAAATAGTGTATAAAGTCTTGGCGATTCAAAATATGAAGATCAGTTAGTCAAATTTTTTATATATAATAAATATTTTGCCTTCACTTTAAAAATTCAAGAGAGAACAGACTATGAGAAACAAAGATTTCCATAAATATTTTAAATGTATGACAATTGATTTTTTTTTCATTCTTTAAATCTCATGCAGCTGGTTCCACGGCGGTGCACATGGGTTTATGTAATGAACAACTGGCTGCTTTCTATATCAGGTCAGATAAAACCAAAGAAAACATTTACCGAGCATTCCAGAATATTTGAATGTTTCAACTTCTCCATCATGAAACTCTATACACTTCTATGTGTGTGTTTCACAGGTAAAGCATCT[C/T]AGCTGTACTCCTACAACCTGACGGGGCTCTTTGAACAAGCGCGACAGATGCAGAAGTTACCCGTTGCCATTCCAACACACAAACTCCCAGACAAAATCATCCCGCGGTAAGATTTAGATCATAGATGTTAAAGTCAATTCCTGGAGGGCCGCAGCTCTGCACAGTTTTGCTTCAGCCCTAATCAAACACACCTGATCCAACTAATTAAGGTGTTCAAAAGAGTCTTGAACACCTTGACTAGTTGCATCAGCTGTGTTTGATTAGGGTTGGAGCAAAACTGTGCAGAGCTGCGGCCCTCAAGGAATGGAGTTTGACAGCTATGATTTAGATGAAACGTTTTAGGATCGTTTTATAAATTTAATCAGTTATCATTCATACTATTTTTTAAAATTTGATTTATCTAAAGATTTACTTAAATAATTGTGACTGATTTACAATGTGTTCCATTAATGCATTTGTTTCAGGAAGTTTACCGTGTCTAATAAAATACCAGAAACAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36411
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093004 | Nonsense | 652 | 864 | 27 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 24486353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24639795 |
GRCz11 | 17 | 24658196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACAGTTTAACATGAATTGTTTGTGTATGTATGTAGTGCGAAACCCGTA[C/A]ACAGGTCACAAGTACCTCTGTGGAGCTTTCCAGTCCAGTGTAATGCTGTT
Long Flanking Sequence:
CAGAGTGTGGACCAAAAGTGCTAGTGTGAAAGCACCCTTATTAACTTATTTTTAAATAACTAATTTCTGTTGTCTTTGCCATTATGACAGTATATAATATTTCACTAGTTATTTTACAAGACTTTTTTCAGCTTAAAGTGCAATTTAAAAGGCTTGACTAGGTCAATTTGGTTAACTAGGCAATTCATTGGGCAACAGTAATTTGTTCTGTAGCCAAATTTTTTTAATGGGGATACACGTATTGACCTTAGCAGTTTTTAAACTAAATTTAAACAAAATTTTCTCCAGAAGGTTAAAAAAAGTTGCAAAAATTGTGAAATTTTTCTTTGCTGTTAAACTTTACTTGGGTAATATCAGCAAAAGAATTCAATCTTCACATATACTATATAGCCACATGATATAAACATTATAATCACAAATTGCACAAAAGTAGTGCAATTCTTAGCATGAATACAGTTTAACATGAATTGTTTGTGTATGTATGTAGTGCGAAACCCGTA[C/A]ACAGGTCACAAGTACCTCTGTGGAGCTTTCCAGTCCAGTGTAATGCTGTTTGAATGGGTGGAAGCCATGCAGCGCTTCATGCTCATAAAGGTAAGTGAAAGAAACTAAGAAATGACATTAAACGTCTGTAAGGCTTGAAGCTTACGCTGCTATTCTGAACCAATAATTGAAAACAGAAAGCAGTTGAAGGATGGCGTGTTTAAATCAATTACTTATTTGAATCTATTGTAATCCATTAAAGTTGTTATCATTGATAAAGAGAAAGAATCTCAACGCCTTAAAGCAGGCAGTGTTGTTTATTAAGTTAGATGTTTAAATATACAGACAGTAGAACAAAACAAACTAACATACTGGATAGAGAAACATAGCTGTAACTATGCATCAAAGTCTATAACGCTGTGTATTTGTGTCTGTCCAGAGTATAGAGCTCACCCTGCCGTGTCCATTAGAAGTGTTTGAGATGTTGGTGGTTCCTGAACAGCATTATCCTGTGGTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18499
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000093004 | Essential Splice Site | 794 | 864 | 31 | 33 |
Genomic Location (Zv9):
Chromosome 17 (position 24488213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 24641655 |
GRCz11 | 17 | 24660056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGGAATTAATYGTTTGCTTWAAATGATAATTATATATGTCCTTTTCAA[G/T]TGTGTCTGCAGGACAGTGTTTTGGCGTTCTGGAAGCATGGAATGCAGGGA
Long Flanking Sequence:
CTAGAGAGCATTTGATTGGTCATGATTTGTTGAGAAACATATGAGGTGATGTGAAAAAGCCATTAATACATTTAGGCAGAAGTGACAAACTAAAAGCCTTAGATGTTATATCACTTTTATATCTTCTAAATGCCAATTGTGTCACTGTTTTGGAGCACACTAGCGTATAAATATCCTTAAAACTAATAATACTAATAATAACATCCAAAAAACATTATTTTCATTTCATTGGACCTTTAAAGCTTTCGTTGTTTTTGAGTTCACTCAATGTCCCTGATATCCTTTATCCAGCAGCTTCCACTCACAGTGTGTTTCGGTATTTTGCAGGATGTATAAAGTTGGTAAATTTACAAGGCAGATTAAAATCCAACAAGAAGTTGTCAACGGAACTCACTTTTAACTTCCAGATTGAGGCAATAGGTAAGGATTAAACTAATGTAAAATATTGACTGTGGAATTAATCGTTTGCTTTAAATGATAATTATATATGTCCTTTTCAA[G/T]TGTGTCTGCAGGACAGTGTTTTGGCGTTCTGGAAGCATGGAATGCAGGGAAGAAGCTTTAAAAACAGTGAGGTATGTCATGTAGTTCTGTAGTTCTTAGTTTCTTAAGTAGATTTCTACTTTAAGTCTATTTTCTTCCAAACTAAATGTTTTTGCTATTGTTTTGTACAACACAGTACATTTTAATTAAAGGAAAGCAAAAATCCTATCAAAGCTACATGCTAATTCATACTGGAAACATGGTGATACACTTATTTCACATGGCCGCCATTTCAAAAAACGAAAGAGAGACTGCGGTGGGAAGAAACCCGAAGGTATAAGATCAGCACTATAAACATTGCAACAACATGCTGTGGACTACAAACCTCCAGCTGTTGCTGTCATTTCAAAGTGCAGATATGATGTAAATATCACTTTAATATCATTCAGTTAAGTTTCATTTAAACTATTTAAAGCATATTAGGTATCAAACAAACTGACAATAATATGCTTAAGTTCATA
Associated Phenotype:
Not determined