Busch Lab

ZMP

myh10

Ensembl ID:
ENSDARG00000000103
ZFIN ID:
ZDB-GENE-030616-162
Description:
Novel protein similar to human non-muscle myosin, heavy polypeptide 10 (MYH10) [Source:UniProtKB/TrE
Human Orthologue:
MYH10
Human Description:
myosin, heavy chain 10, non-muscle [Source:HGNC Symbol;Acc:7568]
Mouse Orthologue:
Myh10
Mouse Description:
myosin, heavy polypeptide 10, non-muscle Gene [Source:MGI Symbol;Acc:MGI:1930780]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa2305 Essential Splice Site F2 line generated Not yet available
sa5750 Essential Splice Site F2 line generated Not yet available
sa33803 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20627 Nonsense Available for shipment Available now
sa40631 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa2305
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046359 Essential Splice Site 171 1992 2 42
ENSDART00000046359 Essential Splice Site 171 1992 2 42
Genomic Location (Zv9):
Chromosome 6 (position 7483048)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7409064
GRCz11 6 7566233
KASP Assay ID:
554-2901.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCATATCTACGCCATTTCCGAATCGGCATACAGATGCATGCTTCAAGG[T/C]AAGACCACATTTGWGAAGTATTCCTTCAGATTCCTTCCTTTCAGTGGCTC
Long Flanking Sequence:
GTGTACAGTTGCAGTTTTGTATGTGAAACCGCCGAAAGTAAAGGGTTAATATCTTGTAACTGTCTTCTGTAATTTAGTGCGTGATCGCTGCACGACAGCTGCAATCATTGTGAATGCATGCCAGCATTGCTCGGGAAAAATACCTTCATTGTGTTTCAATGTGTACAATATTCTGGACATGGAATAATAATGCTAATATTAATATTAGAAACTTGCTGTTTTACTGTCCCTTCATGAACTGCAACAAAATGTAAATGTAAAATGTTTTAAATTAATAATGAACAGTAAAGTTTATTGCATCTCATTAACAAAGTGTTTATGTTTTTGGCTTGTGTTGCACAGACATACTCAGGACTCTTCTGCGTGGTCATAAACCCATACAAAAACCTCCCCATATACTCTGAGAACATCATCGAGATGTACAGGGGCAAGAAGAGGCACGAGATGCCGCCTCATATCTACGCCATTTCCGAATCGGCATACAGATGCATGCTTCAAGG[T/C]AAGACCACATTTGTGAAGTATTCCTTCAGATTCCTTCCTTTCAGTGGCTCTATGTGTTAGAAAAACAGCACAGAATTCTGCACTCCCCCTGATGATATTGCAGTGAAAGTAATAGTGGCTGTGTTGTGTTTTCTTAATCTTTGTTCAGCATTCGCTTTGATGGATGTAGTGTAGATGAGACCACCCTGTGTTGAATTAAAAAAAAAAAGTCTCTCTCTTTTGTGCTTTTGAGCAAGACTAAATTTCCTACATGAATTCCATACTCAAAGCTGTATCTGAACTTACGGCAAGTTTCAGCCAACCTTAAATTGTATTGTCGGTACACTACCAGACAAAAGTCTTGTCGCATGTCCAAGTTTTAGGAACAACAAAAAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTGTATGATGGGTAAAGGCCTCTAGATTTCACTTATTTTACCAAAATAAAATATGTTCATGATTTTTAATTACTTAATTATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5750
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046359 Essential Splice Site 171 1992 2 42
ENSDART00000046359 Essential Splice Site 171 1992 2 42
Genomic Location (Zv9):
Chromosome 6 (position 7483048)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7409064
GRCz11 6 7566233
KASP Assay ID:
554-2901.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCATATCTACGCCATTTCCGAATCGGCATACAGATGCATGCTTCAAGG[T/C]AAGACCACATTTGWGAAGTATTCCTTCAGATTCCTTCCTTTYAGTGGCTC
Long Flanking Sequence:
GTGTACAGTTGCAGTTTTGTATGTGAAACCGCCGAAAGTAAAGGGTTAATATCTTGTAACTGTCTTCTGTAATTTAGTGCGTGATCGCTGCACGACAGCTGCAATCATTGTGAATGCATGCCAGCATTGCTCGGGAAAAATACCTTCATTGTGTTTCAATGTGTACAATATTCTGGACATGGAATAATAATGCTAATATTAATATTAGAAACTTGCTGTTTTACTGTCCCTTCATGAACTGCAACAAAATGTAAATGTAAAATGTTTTAAATTAATAATGAACAGTAAAGTTTATTGCATCTCATTAACAAAGTGTTTATGTTTTTGGCTTGTGTTGCACAGACATACTCAGGACTCTTCTGCGTGGTCATAAACCCATACAAAAACCTCCCCATATACTCTGAGAACATCATCGAGATGTACAGGGGCAAGAAGAGGCACGAGATGCCGCCTCATATCTACGCCATTTCCGAATCGGCATACAGATGCATGCTTCAAGG[T/C]AAGACCACATTTGTGAAGTATTCCTTCAGATTCCTTCCTTTCAGTGGCTCTATGTGTTAGAAAAACAGCACAGAATTCTGCACTCCCCCTGATGATATTGCAGTGAAAGTAATAGTGGCTGTGTTGTGTTTTCTTAATCTTTGTTCAGCATTCGCTTTGATGGATGTAGTGTAGATGAGACCACCCTGTGTTGAATTAAAAAAAAAAAGTCTCTCTCTTTTGTGCTTTTGAGCAAGACTAAATTTCCTACATGAATTCCATACTCAAAGCTGTATCTGAACTTACGGCAAGTTTCAGCCAACCTTAAATTGTATTGTCGGTACACTACCAGACAAAAGTCTTGTCGCATGTCCAAGTTTTAGGAACAACAAAAAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTGTATGATGGGTAAAGGCCTCTAGATTTCACTTATTTTACCAAAATAAAATATGTTCATGATTTTTAATTACTTAATTATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33803
Status:
Mutation detected in F1 DNA
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
ENSDART00000046359 Essential Splice Site 435 1992 12 42
Genomic Location (Zv9):
Chromosome 6 (position 7525151)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7451167
GRCz11 6 7608336
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAAAGTGGGCAGAGACTACGTACAGAAAGCCCAAACTAAAGAACAGG[T/A]AATGAGATAATCACTTCCCCTTTGTAAATCTGTCAGATCACCACCCCTTC
Long Flanking Sequence:
TGCTCGCGTGGGTTTCCCCCGGGTTCTCCGGTTTCCTCCCACAGCCAAAAAAACATGTGTCATAAGTGAATTGATCAATTTAAATTAACACTATAGTCGAATTCCTAACCAGCAGTATTTTTTTCTACACAGCAAATTTGATCTGTCATCAACTCTAAAAAAATGGTGGATAGTTCTCCAGACCTACCTGAGCTCAAACTCCCTTCTTGCCCAACAAACGGGAGGGAGCCCCGGACTCAAGGATCTTATGAGCTCAGGGCTCTCTCCCAGGACAGCTTCCCAAACTCACTTTATAATCAATCATCAGCTATGTGTGAACTCTTGAACAATCCTTTAGAGGACTTGGATTTTAAAAGCATTTGTGTTTTATGTGTTTTCAGCTGCTCAAAAACTTTGCCACCTGCTCGGAATGAATGTCATGGAGTTCACTCGTGCTATCCTGTCTCCAAGAATCAAAGTGGGCAGAGACTACGTACAGAAAGCCCAAACTAAAGAACAGG[T/A]AATGAGATAATCACTTCCCCTTTGTAAATCTGTCAGATCACCACCCCTTCAGCTATAAGACAATGTTTTCTTTTGGATCCTGATAATTTCCCTTTGTACCTCTCTGTCCATTTACAACAATAGGCTTACAGTGTCCTGTCATAAAATTGTCATCACTATTATTCACATTTAACTGTGCAAATGAATGCTTTTCTTAACATTTAAAAGTCCTGTGATATTAAAAAAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAGCTAGTTTTAAGGATATCTATTAGCTAGCTGTTCCAAAACAGTGAAAATTCACATTTACACTTCCTGACAAAAGTCCTGTTGTCAATTCCAGTTGTAAGAGCAGCAAATAATAACTTCTAGTTGATCATTTGGAAAAGTGTCAGAAGGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20627
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046359 Nonsense 518 1992 14 42
Genomic Location (Zv9):
Chromosome 6 (position 7528713)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7454729
GRCz11 6 7611898
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCAGCTCTTCAACCACACCATGTTCATCCTGGAGCAGGAGGAGTA[T/A]CAGCGGGAAGGCATCGAATGGAGCTTCATCGACTTCGGCCTCGACCTGCA
Long Flanking Sequence:
TATAAAAATAAACTTCCTAAAGATTTGAAGATATGACAATTGTAAAACTTAATACATTTTGTTGTTATAAATTAAAAAACAACAACAAATTAATTTTGAGTACAAAACCTAGTTATTGCTCATTTGAGCTTTCTTCTTTCAGGTTTCATCTCAGAGCTGGACTTTGCTTTGGATAAGATGCATCTGCTAAATTGAATAATATAATTATGACTTTGTTAGGAAACCAAATAACAAGGTTTACAGTAAACAGTGTAATTGGACACCCACTCATAGCTGCGATATCCAGTTAGTTGATATCGATGTTGCAGATCTTGGTTAAAGAGCCAATTAGGCCTGTTCTGGGGCTAAAAATACTACGGACAAAGACAACTCATTCATGCTTAATTCTCTTCTATCTCTCTGTAGCTCAACTCATTCGAGCAGCTTTGTATCAACTACACCAATGAGAAGCTCCAGCAGCTCTTCAACCACACCATGTTCATCCTGGAGCAGGAGGAGTA[T/A]CAGCGGGAAGGCATCGAATGGAGCTTCATCGACTTCGGCCTCGACCTGCAGCCCTGCATTGACCTCATTGAGAGACCCGTGAGCAGCTATTCGCAAATGAAATTGTCCTTAAATTGGTTGATAGAAATGTTTTTGCTCCTACTTTATATTACAGGGTGACTGCGGGGTCTTAAATAAAAAAAAAAACGAATTTTTTTACAATATTTACTGTACACAATAAGTACATTGTAACTGAATAATTTCAGTGTAAGTACATATTAGTTATGGACACTTGATATGAATTAGGACTATATTTTCTAACCCAGATTTGAATGGCAGTAAAGAATGTTTTCCTTTGGCTTTTCTGCAAATATAGTTGTCCTAAATGGTCATTTTTTTGTACTTCTTAGGCAAATCCTCCTGGCGTGTTGGCTCTGTTGGATGAGGAATGCTGGTTCCCCAAAGCCACAGATAAAACCTTTGTGGACAAACTTGTTCAAGAGCAAGGCACCCATGGAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40631
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000046359 Nonsense 1832 1992 39 42
Genomic Location (Zv9):
Chromosome 6 (position 7569259)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 7495275
GRCz11 6 7652444
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTAAAATCCAAGCTGCAGGAACTCGAGGGATCCGTCAAATCAAAGTTC[A/T]AGGCCTCTATCGCCGCCCTGGAGGCAAAGATCCTCCAGCTAGAGGAGCAG
Long Flanking Sequence:
CTGGAGGTGTCAGTGGGTTTGGTTAAAAAATACTTTAGTATTTACTGTAAATTACTTTGGTATACTTTCATGTGGGTGAGTGATGAATGACAATAGATCTAGTGGCAGATATGGCAGCCTCTATTACTTTTTAGCTTGCACTTTTTGTTAACATTCATTATTATTTATTAGTTCAGGATATATGTGTTTTCAATCATAAACAGATGTATCAATACAATGTTAACATATGCTTTCTCTGTGAATTTATATTTTAAGTTTTTACTCCGAATGTCTCATCCAAAGCGTTGGAATTGCTCTGTAGTTCTGATCTTTGTAAGTGTTTAGATGTTTAGTGAGAGCTGCTGTGTGTGAATGTTCAGGTGGACACCCTGAACACAGAGCTGGCAGGAGAGCGCAGCGCTGCACAGAAGAGTGAGAACGCACGTCAGCAGCTCGAGCGCCAGAACAAGGACTTAAAATCCAAGCTGCAGGAACTCGAGGGATCCGTCAAATCAAAGTTC[A/T]AGGCCTCTATCGCCGCCCTGGAGGCAAAGATCCTCCAGCTAGAGGAGCAGCTCGAACAGGAAGCAAAGTACGCAAACGTTTTCACAATCACTACTCAGAAATGAACCGATTGAGTTATTGTTTTCTCTAATACAACAGGTTACTTGAGTAAGGACATTTTTTATCAGTGTTTTGCTGAAGCTGAATGCTTGTCTGATCACAGGGAAAGAGCTGCAGCTAATAAGATTGTGCGTCGCACAGAGAAGAAGCTGAAGGAGGTGTTCATGCAGGTGGAGGACGAGCGGCGCCATGCAGACCAGTATAAAGAACAGGTGAGATGAAGCTTCTCGCACACTGCCAGTCAAAGCAAACGAAACACCTCTGACACCAGTGTTGTGTATGTTTAGATGGAAAAGGCCAACTCGCGCATGAAGCAGCTGAAGAGGCAGCTGGAGGAGGCTGAGGAGGAGGCGACGCGAGCAAACGCCTCCCGCAGGAAACTGCAGAGAGAGCTGGATGAC
Associated Phenotype:
Not determined