ZMP
LOC566845
Ensembl ID:
Human Orthologue:
MYLK4
Human Description:
myosin light chain kinase family, member 4 [Source:HGNC Symbol;Acc:27972]
Mouse Orthologue:
Mylk4
Mouse Description:
myosin light chain kinase family, member 4 Gene [Source:MGI Symbol;Acc:MGI:3643758]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17085 | Nonsense | Available for shipment | Available now |
sa32817 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12023 | Nonsense | Available for shipment | Available now |
sa39738 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39739 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17085
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 |
---|---|---|---|---|---|
ENSDART00000122138 | Nonsense | 185 | 769 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 431465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 398133 |
GRCz11 | 2 | 411000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGAAGGAACCCAAAGGTTTTCATCTGAGCCTCAAAGGCCTCAAAGCA[C/T]AGAGGAAGAAGAAACCACCAGATTCAGCTGGTAAGTACAAAAACAAAACA
Long Flanking Sequence:
CTCATTTAAATATCTAAAAATGCTTAACTCAAGTTTTTTGTTACACAAAGTGTTTTGTTTTTAGAAATAAGTGAGTTTTTTCTTAAAATAAACAAGCAAAATAATCTGCCAATGGGGGAAGTTAAATAATAATATTCCAAACCAAAAGCAAGATGATTGTCCTCCCCCCAGCATTGGCAGATTATTTTGCTCTCTTCATTTTGACTTATTATTTCTGAAAACAACACAATGTTGTGTGCTTGTCTAAAAAATTCTTCTTGATTTAATTTTTTAGATATTTGGACTAGAAACAAGACAATAACTCATATTTTGCAGTGTATATTCTCACAGCATTTCACAAGAGTTGCTTGCTGACTCTAAATGAATTGTACAAATTCGCTTCACATATGAAAGACCTGCAAGTTTATTTACTAAGGTGAAATGGTTTCCTCTGTTTCCTTTTTGATTTAAAGCTGAAGGAACCCAAAGGTTTTCATCTGAGCCTCAAAGGCCTCAAAGCA[C/T]AGAGGAAGAAGAAACCACCAGATTCAGCTGGTAAGTACAAAAACAAAACACACATACAAGATATAGCCTTGTTTTCAGAAATAATGAGTCAAAATGAAGTGCTTATTACTTTAAAACTAGCTAAATAATCTGCCAATAAGGTGAGTAAAATAATCCTGTTTTGTCTTTTTGACCCCTCTGACCCAATTGGCAGATTATTTAGCTTGTTTTAAGGGAAAACTCACTTAATATTGGCAAATTATTTCTTAAAACAAGACATTATGTTTTGCTTGTCAAGAAAAAGCTTCATGATTTGAAAATTAGTAGATATTTGGACTAGAAACAAGACTAAAAATCTAAGTATGAAAAGCACTTATTGCAGTGTGCCCCTGTATACACTTCTAGAGATTGTGAATTATGTACCCAGAGGTACGTATGGCTGCATTTTGTCTTTAAATCAAACGCTACTTGGGGCGTTTGCTTTTCGTGCTACCAGCTGCCCGCTTACCTCCATACAGACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32817
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 |
---|---|---|---|---|---|
ENSDART00000122138 | Nonsense | 276 | 769 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 433163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 399831 |
GRCz11 | 2 | 412698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGAAGACGAAAGTAGAGAAAAAGGTGACTCTGGATCTCAGAGAAGAA[C/T]AGAAGAACATCCCAGAGACGAACACAGAGGAGATCCGAGAAGAAATGAAG
Long Flanking Sequence:
TGAGCCTGGGTTGTCATTGGCAGATTATTTTGCTTGTTTTAAGGAAAAACCGGCTTAATTTTGACTCATTATTTCTGAAAGCAAAACAATAGTTTGTACTTGTCTTGAAAATGCTTCTTAATTTAAGACTTTTAAGATGTTTAGACTAGAAACAAGACACAAACTCTGAATAATCAAAGCATTTTTGCAGTGTAGTCAGTATCAGAGTGTGCAACCCAGACAATACACTGAAACGCACGTGTTACGCTCATATTCCAGCAGACAAAGTCTTTCTGAGGAAGCAGGCACTGTTGCTTGAAGAAGTTCAGAAACTCAACCAGGAGAACGCCGAGCGCTCCAAACCAGCCCAGACTCAAGATAATGACCTGCAGAAATCAGAAGATGCCTCGGTTACTCCACATCTGCAGGACATTATCCTGGAGGAAGCCAAACCGGTGGAAGACGAGCCGAGAAAGAAGACGAAAGTAGAGAAAAAGGTGACTCTGGATCTCAGAGAAGAA[C/T]AGAAGAACATCCCAGAGACGAACACAGAGGAGATCCGAGAAGAAATGAAGAAAGCAGACACTGAGGAAATCCTGCTGAAGACCACAGAAGTGCTCAAAGATCAGAAAACAGACGATACGGAGAGCAAGACGACTACTGAGGGCCCTTCAGAAGCTGATAATATTGACACAAAAGCTACTGAGGGCCCTTCAGAAGATGTTATTACTGACAAAGAGACTATTGAGGGCCCTTCAGAAGCTGATATTACTGACACAGAGCCGCCAACAGCAACTGAGAACTCAGAAATAAGGTGAGCTTAAAGTCTGCATGAACTGTTGTTATTCTGTATTGTAGTTCCTGAGAAACTGAATATTAATGAGAAAAAAGTGGGCGTGGTTTGTTTTTATCTACTGCAAGCTGATTGGCTGTGGAAAAGTAGGCGTTTCATTCAGAGAGACGGGAAAAGGGTTTTTGGAGTTATTACAATCTAACAGACTCCTCCTCCTCCTCCTCACTATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12023
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 |
---|---|---|---|---|---|
ENSDART00000122138 | Nonsense | 440 | 769 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 434057)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 400725 |
GRCz11 | 2 | 413592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTAAAGCYGACGGTGTGGAGATCCAGATCGACTTCAGCAAACTGAAG[C/T]AGCAGAGCTTTRAGGATGAAGATGATGAAGATCACGGCGATMACTTCTTC
Long Flanking Sequence:
AAGCTGATTGGCTGTGGAAAAGTAGGCGTTTCATTCAGAGAGACGGGAAAAGGGTTTTTGGAGTTATTACAATCTAACAGACTCCTCCTCCTCCTCCTCACTATTTCTGTTTGTTGTTATGGCGATGTCAAAACTGACAGTTTGAGGGGCGTGGTTATGTGTTAGCCACACCCAATACCTAACAAAGCCTGATTGACTGCAGTGGAATAGTTTAGTCAACTGACAACAGATCCAGTAATCCTGAGTTTGTTCATCCAGAGTAACAGTACAGGCCTCCTCTGTCGTGTCTGTGTTACAGCAGCGAGTCTGAACAGGCAGATGAAGTGACGACCAGCAGCAAGCGACGCGTGACGGAGGAAGATCTGGGTTTGGAGGACCATAAAAAGAGTCGCGTTGAGGACGGAGAACAGCAGGAGCCGGAGCCGCCGGAGCCTGAAGATCTGCGCGCTGTGTTTAAAGCCGACGGTGTGGAGATCCAGATCGACTTCAGCAAACTGAAG[C/T]AGCAGAGCTTTGAGGATGAAGATGATGAAGATCACGGCGATCACTTCTTCATTGGTGAGATTCTCATTTGAGTCCAATATATATAAGCTTGGCAGGGTGACTTTTAAAATTAGGATAGCAATCTTGCGATATGTCTTAAGGATGCTGGGAATTGTTTTTTATATATTGTTGTTACAGGAAAAGACGTTGTTTTAACAAGAATAAAATCTAATTTTCAAGAAAAGATGTAGTTTTAATGAGAAAATATCTTATTTAATGACATTATTACAAGAAAATTATGTGTAAACTAAATAATTATGTCGTTTTAACAACATATTTTATTACAAGTAAAAACATCCCGAAATTACAAGAAAATATGTTGTCTTAATGATGAAATATGTTGTTTTAGCAACGTAATATCTCCTTACTACGAGAGAAGAGGTTGTCTTAACGAGAAAAGATCTTGTTTTAGTGACATATCGTTATTACCAGAAAAGATGTTGTTTCAACAAGAAAATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39738
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122138 | Essential Splice Site | 675 | 769 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 443654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 410070 |
GRCz11 | 2 | 422937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCAGAGTAAATGGGTGTGTTTTTCAGTGTGTGTGTTGTGTGTTTTCT[A/G]GGCTCAGCGGTTTGTCGCCGTTCCTCGGGGACGACGATAACGAGACGCTG
Long Flanking Sequence:
TATGATTTTGTGTCCTTCAACACAGACATGTGGAGTTTGGGCGTCATCACGTACATGCTGTGAGTCTTGTGTGTGTGTGTGTGTGTGTGGAGGATAGTGAGTAAAATATGTTTATATTGGCTTCAGAGAAGCTTTAAAGCATAAAAAGTAATTTATTTTAAGCTTTAAACAATGAACAATACTAATACCAGCATTTATTGTTTACTATTTATTAAATTAATTAATAAATATCAGTTATAAATATATAATAGTAAAAATAAACCTTTTCTCATGCATTAATAAAACTAACATTAGTTAATGCACCGTGAGTTAACATGAACTGAGCTTATTTTCACTTAAAAATGTGAACAAATATGAATAAATCCTGTCATAAATGTGTTATTCATGGTTAGTTCATGTTAGTAAATGCGTGATCTAATCTGACCTGATCATTTCTCAGATTGACTAGTCATTTCAGAGTAAATGGGTGTGTTTTTCAGTGTGTGTGTTGTGTGTTTTCT[A/G]GGCTCAGCGGTTTGTCGCCGTTCCTCGGGGACGACGATAACGAGACGCTGAACAATATTCTGGCCTGTCAGTGGAACTTCGAGGAGGACGAATTCTCTGAAGTCTCAGCAGAAGCCAAAGATTTCATTTCCAAACTCCTGGTGGTGGATAAAAGGTAAACAGGAGGATAAAACACACATTAAAGGGACGTTTAGCTTTGTTTTTCTGCACTTGATGTGTGTGGAAAGAGTTGAGAAAGAGTCAAAGCAAAAACATTGTTTATTATAAATAGTGTCGATATTTATGAAGGTCAGCACAAGTTTGATAAATGCAGAGCCTAAAATATGAACAAAATGTGAGTATTTTATGTGAAACAGCATTACCTTTTATATTAATTCAATCACGTACTACATGCATTTAAAAACACATAAAACTGTTGTCAATAAAAGGGAGCGTTAGAAGAGTTTTGACATTCAAAAGCAAAGAAAAATATATGCAAAAAAAAAAAAAACGATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39739
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122138 | Nonsense | 699 | 769 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 443728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 410144 |
GRCz11 | 2 | 423011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGGGGACGACGATAACGAGACGCTGAACAATATTCTGGCCTGTCAGTG[G/A]AACTTCGAGGAGGACGAATTCTCTGAAGTCTCAGCAGAAGCCAAAGATTT
Long Flanking Sequence:
GTGTGTGTGTGTGTGGAGGATAGTGAGTAAAATATGTTTATATTGGCTTCAGAGAAGCTTTAAAGCATAAAAAGTAATTTATTTTAAGCTTTAAACAATGAACAATACTAATACCAGCATTTATTGTTTACTATTTATTAAATTAATTAATAAATATCAGTTATAAATATATAATAGTAAAAATAAACCTTTTCTCATGCATTAATAAAACTAACATTAGTTAATGCACCGTGAGTTAACATGAACTGAGCTTATTTTCACTTAAAAATGTGAACAAATATGAATAAATCCTGTCATAAATGTGTTATTCATGGTTAGTTCATGTTAGTAAATGCGTGATCTAATCTGACCTGATCATTTCTCAGATTGACTAGTCATTTCAGAGTAAATGGGTGTGTTTTTCAGTGTGTGTGTTGTGTGTTTTCTAGGCTCAGCGGTTTGTCGCCGTTCCTCGGGGACGACGATAACGAGACGCTGAACAATATTCTGGCCTGTCAGTG[G/A]AACTTCGAGGAGGACGAATTCTCTGAAGTCTCAGCAGAAGCCAAAGATTTCATTTCCAAACTCCTGGTGGTGGATAAAAGGTAAACAGGAGGATAAAACACACATTAAAGGGACGTTTAGCTTTGTTTTTCTGCACTTGATGTGTGTGGAAAGAGTTGAGAAAGAGTCAAAGCAAAAACATTGTTTATTATAAATAGTGTCGATATTTATGAAGGTCAGCACAAGTTTGATAAATGCAGAGCCTAAAATATGAACAAAATGTGAGTATTTTATGTGAAACAGCATTACCTTTTATATTAATTCAATCACGTACTACATGCATTTAAAAACACATAAAACTGTTGTCAATAAAAGGGAGCGTTAGAAGAGTTTTGACATTCAAAAGCAAAGAAAAATATATGCAAAAAAAAAAAAAACGATATATATATATATAATATAATATAATATAATATAAAATATATATTGCATTACATAATATAATGTATTAATTTTCTTGTTCC
Associated Phenotype:
Not determined