ZMP
si:ch211-120p12.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate mixed lineage kinase 4 (KIAA1804) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
RP5-862P8.2
Human Description:
Mitogen-activated protein kinase kinase kinase MLK4 [Source:UniProtKB/Swiss-Prot;Acc:Q5TCX8]
Mouse Orthologue:
BC021891
Mouse Description:
cDNA sequence BC021891 Gene [Source:MGI Symbol;Acc:MGI:2385307]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38936 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42194 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31928 | Nonsense | Available for shipment | Available now |
sa31927 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38936
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 |
---|---|---|---|---|---|
ENSDART00000110070 | Nonsense | 521 | 1017 | 6 | 11 |
ENSDART00000144282 | Nonsense | 498 | 959 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 23869446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23515106 |
GRCz11 | 13 | 23645556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCAGCACAAAATCACAGTTCAGGCCTCTCCTACGATGGACAAGAGA[C/T]GAAGTCTCAATAGCACAAACTCAAGCCCTCCCAGCAGCCCGACTCTGATC
Long Flanking Sequence:
AATATCAGATGAATTTATTTCAGTAAATTGGTGAAATAAAGAGTTAATCCTGACACATTCTATTTCACAAGTAACAGCATTTCATACTGCTCATAATTTACCCTAGGTCAGCAAATAGTCTTGAGCATTCATAGACTGGCCTTTCACACTTTATATTTATAAACCCTGTCCTATCGTCCTTCTATCGTCCGTTCTTTATTTTCAGCACACAGGTTGCTAACCCCACCTTCTATATTTCAAGTGAAATTTGTTGCAGTTAAAATTGGCAAAATGATAATCCAAGGTTAAGCAAAAAATGAAAGACCCAATTGTTTTGCATCACTTTATTGTTTTTCACTGGAGCATTAAGTGTGATGTAAAAACTTGTTATTGTAAAGTGTTGGAAGAAAATTTGGAAGAAATGTTTACAGTGGTATTAGTAAATACTAATCTTAGGTGTATATATAAAAGATTTTCAGCACAAAATCACAGTTCAGGCCTCTCCTACGATGGACAAGAGA[C/T]GAAGTCTCAATAGCACAAACTCAAGCCCTCCCAGCAGCCCGACTCTGATCCCTCGCCTCCGTGCTATTCAATGTGAGTACCCACTCTTCTACACTCTTTACCATTTTTTCATAACTGTATATGTGAGATTTTAATTAACCCTTAATAGCTTGATATGCAAGTTAAAAATAAATATATTTTAACCTTTTAGAATTGAAATTCATTCAAATCTAAGAAATGTTTGAGTATAATTTTTCTGTTGTTGAGTATCGTATTTTATTTAGGTTATGGGATATATAGTAAACATGAATCTAATTAATTTAAAGGTCCAAAAGGTAAGATGAATTTCTGATAGCTTATAAAACAGAAAAACACAACTTGCAAAAAAAAAAAGCAAATAAATATTAGTTGTTACTCCTATCACAAAAGAGCCTGTTTTTTTAAACCATTGTTGAGTTGTTTAATTTTGGATAATGCAATGTAATTTCTTAAAACTTGATTTTTTATATTTTAACAGGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42194
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110070 | Essential Splice Site | 544 | 1017 | 6 | 11 |
ENSDART00000144282 | Essential Splice Site | 521 | 959 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 23869373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23515033 |
GRCz11 | 13 | 23645483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCCTCCCAGCAGCCCGACTCTGATCCCTCGCCTCCGTGCTATTCAAT[G/T]TGAGTACCCACTCTTCTACACTCTTTACCATTTTTTCATAACTGTATATG
Long Flanking Sequence:
ACAGCATTTCATACTGCTCATAATTTACCCTAGGTCAGCAAATAGTCTTGAGCATTCATAGACTGGCCTTTCACACTTTATATTTATAAACCCTGTCCTATCGTCCTTCTATCGTCCGTTCTTTATTTTCAGCACACAGGTTGCTAACCCCACCTTCTATATTTCAAGTGAAATTTGTTGCAGTTAAAATTGGCAAAATGATAATCCAAGGTTAAGCAAAAAATGAAAGACCCAATTGTTTTGCATCACTTTATTGTTTTTCACTGGAGCATTAAGTGTGATGTAAAAACTTGTTATTGTAAAGTGTTGGAAGAAAATTTGGAAGAAATGTTTACAGTGGTATTAGTAAATACTAATCTTAGGTGTATATATAAAAGATTTTCAGCACAAAATCACAGTTCAGGCCTCTCCTACGATGGACAAGAGACGAAGTCTCAATAGCACAAACTCAAGCCCTCCCAGCAGCCCGACTCTGATCCCTCGCCTCCGTGCTATTCAAT[G/T]TGAGTACCCACTCTTCTACACTCTTTACCATTTTTTCATAACTGTATATGTGAGATTTTAATTAACCCTTAATAGCTTGATATGCAAGTTAAAAATAAATATATTTTAACCTTTTAGAATTGAAATTCATTCAAATCTAAGAAATGTTTGAGTATAATTTTTCTGTTGTTGAGTATCGTATTTTATTTAGGTTATGGGATATATAGTAAACATGAATCTAATTAATTTAAAGGTCCAAAAGGTAAGATGAATTTCTGATAGCTTATAAAACAGAAAAACACAACTTGCAAAAAAAAAAAGCAAATAAATATTAGTTGTTACTCCTATCACAAAAGAGCCTGTTTTTTTAAACCATTGTTGAGTTGTTTAATTTTGGATAATGCAATGTAATTTCTTAAAACTTGATTTTTTATATTTTAACAGGGCTCGAAATTGCGACCATTTTGGTCGGATATGCGCCCAAAATTTTGTCTATGCGACCTCAAAACATATTTGGGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31928
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 |
---|---|---|---|---|---|
ENSDART00000110070 | Nonsense | 704 | 1017 | 10 | 11 |
ENSDART00000144282 | Nonsense | 646 | 959 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 23862808)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23508468 |
GRCz11 | 13 | 23638918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATATCGATCTACCTCTGTGGAAAGATGAACCAGGCGAGAACCAGAGTT[C/A]AACAGGAGGAGGAGCTGAGAGCCAGGAGGACCCAACCACCTCCACCAGCT
Long Flanking Sequence:
AGTGTGCAGAGATTTTTGAACACATTGCTTTGAACACACATCTTTTTGAACACACATAAATTTATACACTTTTTCCACAAACACTTGAAATTAATTTAAATAAATAGTTAAAAGGAATAATAGAAAACATTTACTTAACTTTAAGGTTTAAGTTTTTCATGTTGAGCACAAATTAAGATAATTTCTTGAGAACCTGTAACCACTGATTTCCTTTTTAGGAAAAATATGCTAAGAAATATTATTGTAGTATGTCTTTGACACCATTGTGTGTATAGAAGTATGTAATTAAAGTCTGTGATGATGGTTCCAAAATGGGAAAGCAGATTTAAACTGATCTGCTGATCAACTGACGCACTGGCATTTCCCCCCCTCAGGGACCAATAAAGATGAAGCAGGCTCTGCTGATTCATCCGACAACAAACCAAAGCAACTCAAGTTCCCCAACCAGGTGTATATCGATCTACCTCTGTGGAAAGATGAACCAGGCGAGAACCAGAGTT[C/A]AACAGGAGGAGGAGCTGAGAGCCAGGAGGACCCAACCACCTCCACCAGCTCCACCAGCACCACCCCACAGCACACACCCACCAACAGCCTGAAGCGCAGCACCACCCGCCGCCGCACTGACTCTGTTCTCTACGGCTGTGCCTCAATCCTGGCATCTGTCGCATTCGGCTTTGACCTGCAAGAGATCTGTAAGAACCCTGCCAATGAAGAACCTGAGCCTCGTGAGGAGAAGAAGAAAAAAGAAGGCCTGTTTCAGCGCGCCACTCGCTTCCGCCGCAGCACCAGCCCTCCAGGCGGACGTTCGCGAAAAGATGAGATTTCCACAGCACCCGTAAACCTGCTCGCCATGTCATCCATTTCTGAGTGCAACTCCACCAAGTGCCTCCTGCAGTCAGATTTTGAGGGTCCTGGGTTTAACCTGGTTAACGAGACTGGCATTTCGCCTCAGAGTAATGGTACTGGTGAAGGACTGCACTTAACACCTGTACAAGAGCTCTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31927
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 |
---|---|---|---|---|---|
ENSDART00000110070 | Nonsense | 921 | 1017 | 11 | 11 |
ENSDART00000144282 | Nonsense | 863 | 959 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 23859231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23504891 |
GRCz11 | 13 | 23635341 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACCACTTCTACAAAGAAGAAGGCTGACAAAGAGCCTCCTCAAGACAAG[C/T]AGACCTCTGGGGAATCAGTATCTCGACCCAGACCGCTTTCCCTCAGAGGC
Long Flanking Sequence:
AATAATGTAAGCATAAATGCAGAATTATAGCCAATATTTCAATCCAGATGTTTCTTTTTCGTACCAACATCAATATATATTTCAAAACTTGTCATTTTTTTGTCCAATAAAATGCCAAAAAAGGTACAACACTTTGAAAATTGTATCTAAAATCTAGATTATTTAAACTGTATGGTGCAATGTTGTGAGATTTACATTTACTTGTGGCATTTTTATTTTTTAGATTTTATCAGTGTTTTATATGAAGGTTTAAAATATCTAGCTATCTCTCTATCTATTTATCTATCTGTAGGGCGGTAGGTAGATGGGTAGGTAGATAGATGACATATCACTGTACCCTTTCATTACTGCATTAAACTGATTTTTAAGTTCTCAATTGTTGTTTACTGACTTCTCATTTTGCTTTAGTCAATGGAAGCAGCAACTCTCCAGTCAGTCCAGCTGATTCTTCTACCACTTCTACAAAGAAGAAGGCTGACAAAGAGCCTCCTCAAGACAAG[C/T]AGACCTCTGGGGAATCAGTATCTCGACCCAGACCGCTTTCCCTCAGAGGCAAATCTCATTCCTGGAGTCTTCTGAAGAGTCGCAATAAGAGCTATTCTCTGGGACACTACTCTGGGGAGAAGAGTGTCCAAAACCTGGACATGCTGCTCCCTGCTGAGGTCAAAACCGGCTGCTCATTACTGGACATGGACACAGAGGGTCAAAAACGAGACTGCACCGTTCCCCTCTGCCGGATACAGAGCACACCAAGTCGGGGGTCTGTATTCGAACTGGAGAAACAGTTTTTATCCTGAAATAAGCTGCATCTGGAACACAATCCTGTATTTGTTTAGAGTCTGCCTGTTCAACGTAACATTTGTTTTTGTCCACGATTTAAGGGATAGTTCACCCAAAAATGAAAACTGCTGTTAATTTGCTTACTTCAGACATTTCGGATGCTGTTAGTGTTAGTTGAATTAATTTTGTTTCACCTGTATGTTTTTTTGGACTCTCGAAGTGCA
Associated Phenotype:
Not determined