Busch Lab

ZMP

myo16

Ensembl ID:
ENSDARG00000078582
ZFIN ID:
ZDB-GENE-070912-470
Description:
Novel protein similar to vertebrate myosin XVI (MYO16) [Source:UniProtKB/TrEMBL;Acc:B0V082]
Human Orthologue:
MYO16
Human Description:
myosin XVI [Source:HGNC Symbol;Acc:29822]
Mouse Orthologue:
Myo16
Mouse Description:
myosin XVI Gene [Source:MGI Symbol;Acc:MGI:2685951]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa31701 Essential Splice Site Available for shipment Available now
sa16381 Nonsense Available for shipment Available now
sa30913 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa31701
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109288 Essential Splice Site 451 1867 11 36
ENSDART00000133063 None None 339 None 8
ENSDART00000138167 Essential Splice Site 88 1471 2 25
Genomic Location (Zv9):
Chromosome 9 (position 8042877)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8022720
GRCz11 9 8001050
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCTGCTCTACGAGATGCAGAAGCGCTTCGCCAATGACCAGATTTATG[T/A]ACGTAGCAAAATACGTGGTGTGTCAGAGTTCTGTTAACAATCTAAACCCA
Long Flanking Sequence:
TTTTTTCGGATGAGTTCTGGTGATTCATAAAGTGAAAAGTCAATGGCTGTTGGCACTTCAATAGTCGAAAAAAAATATGCATGTATAACAAAAGTAATATCTGTGGATCCTGAGGGTACATGGGGGTCATGACTAACATTTCATATCAATACCTTAAAACAGCAACTTCACCAAAAAATTCACTTGAGGGTAAAAAAAAAAAAAAAACAGATTTTTTTTTATTTTTATAAACTGTCCCTTAAACATTAGACCTGATTATTGACCCAAAAGTGAACTGATTGTTTGCTTATCTTTGTATTGTTCTAAACCCTAATTTTTCATATCTCTTGGAAAACAATAAATAATTTAATATTGCTTTTTATCATGATGAATGTGTTTTATGTTTCAGGTGAAACTGATGCCTCCTGCCCCTAATGATGACCTTGCATCTCTCAGTGAGCTCACAGACAGCAGCCTGCTCTACGAGATGCAGAAGCGCTTCGCCAATGACCAGATTTATG[T/A]ACGTAGCAAAATACGTGGTGTGTCAGAGTTCTGTTAACAATCTAAACCCACAGATCAAGTATAAACACCCAACCTTCAGGTTATGTTTACACAACAGTGCTGGTTTTCTCAAAACTCGTTAGCATTTTCTTTTCATTTCAATAAACAGCCAAAACAAGTCACAAATTGTTGTTAATTTTTATATGAAAGCTCTGTTGCGTAAATGCCTTCTTTAGTCTGTCCCATTCAGAAGAAGTCTTTCACTCTCTGTTCTAACCCACTCTAAAGGAAGTTTCGTCCAGATTTTGGCCCCTGTCACACACTCTCTGGGCTTTCAGCAAGCCTTCCGGTCCAGTCTCCCACACACACAAACGCTGCTGCTGGATCTGTTGTGGGAGGTGTTGGAGAAAAGCCAGGGGCTCTGTTTGTAGCATGGCCAGGGACTGGTGTTTGGATGGCAGCCCTCGAGGTCTCACTGTATTCCGGCCAGAGACTTGAGCAGCACTGACGAGATGAAAAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16381
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109288 Nonsense 808 1867 21 36
ENSDART00000133063 None None 339 None 8
ENSDART00000138167 Nonsense 445 1471 12 25
Genomic Location (Zv9):
Chromosome 9 (position 8090970)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8070813
GRCz11 9 8049143
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCTGCCCTWGAGATMAGCATCCTGGACATCTTTGGCTTTGAGGAATTC[C/T]AACGCAACGCTTATGAACAGGTAAAGGGGAGAGTGATGCGATGACAACAA
Long Flanking Sequence:
TCTATATTTAATATAATATAATTCTAATGTTAATAAGCATGAAGTAGAGTTTAATAATGCATTAGTAAATGCTGTACAAGTACTGTATTGTTCAATATTAGTGTATACATTAGCTAATATTAACTAAAGAAATCTTATTGGAAAGTGCAACTCAAACACGTTGACAGTTTCCAGCAATGCCGTGTGCTTTAGCCCTAGACGTGATGTGAGAAATTTTGACAGAATTGCCCTGACATAACCTTTTTTTTTTTTCCCTTGGAAAACCTGCATGTTTTTTTTTTTTTTTTTTTGTATGTGACCTTTTAGCTGTTTCCCCCCTCTTTTTTCACCTGTAATAGAAATGTCTTTGACACTTTAGCCCAGGGCAAATTGTTGCCTTCAGATCACCAATCAAAGTTAATATGAATGTTACAGTCTTGAAATACAATCCTGTCTTTTTTTGTGACAGAGATCCTGCCCTTGAGATCAGCATCCTGGACATCTTTGGCTTTGAGGAATTC[C/T]AACGCAACGCTTATGAACAGGTAAAGGGGAGAGTGATGCGATGACAACAATGATCGCTACACTTTTAAAGAGATAGTTCAGACAAAAACTGTAAAACTGTCATCATTTACTTGTCACAAACCTGCTTGACTTCTGTTGAACCCAAAAGAAATTATTCTGAAGAAAGCTGGAAACCTGCAACCATTGACTTTCATAGTATTTCTTTTTCTTACTACCGAAGTCAATGATTACACATTTTCCGGTTTCTTAGGAATAACTGTGTTCAACAGAAGAAAGAATCTCATAAATGTTTGATAACCACTTGAGGGTGAGTAAATAGTCTGGAAATTTACATTTTTTGGGTAAACTGTCCCTTTAAGGAACAACACTGCAGGCAAAAACAGCTTTTTAATACACATTATTAAGCTTTTTCTTAGTCTAATTTATCCAACATTAATTTGTTTATTTTGTTGTTCAGTGCATTTACAGTGCATTAACGTTTTTACTGAGCAATTTTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30913
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109288 Nonsense 1675 1867 32 36
ENSDART00000133063 None None 339 None 8
ENSDART00000138167 Nonsense 1294 1471 23 25
Genomic Location (Zv9):
Chromosome 9 (position 8164374)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8144217
GRCz11 9 8122547
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCTACCGCCCCCCTTCTCACTTCCCCTTCCCCCCTGAGCCGAACTTCT[T/A]GGCCCTGACTCGTGCAGCTTCTGTGGCTAGCACAGAATCCCCCAAAGTCT
Long Flanking Sequence:
GATAGTGTCAACTCCAGTGGTGAAGCCTGAAGCCGTCAATCCCACTCCACTACCTGCCCCAGTGCTAGAAATTAAGAGGCCTGTGACCCTGATTGAGCAGTCAGGCACACTTGGAGGAAAGCAGCAGGGCAAGGATGGGATGCCATGTGACATCCCAGCTCCATTCCCCAACCTCCTTCCACACCGTCCACCACTTCTGGTCTTCCCTCCATCTCCTGTGACCTGCTCTCCTGCATCAGATGAGTCCCCTCTTACCCCTCTTGAGGTGAAAAAGTTGCCAGTGTTTGAGACCAATCTCAACTACAGCAGTCAAGATGGGGGCAGCCCACTGTCCCCCCAGTACACCCGACAAAGGGCTGACTCTTCCCCAAGTCTTTCCATCCTGATGCCAGACAAGTCCACGCCACCATTGACTCCTCCTCCCCCTCCTCCTCCAGCAGTACTTCCACCTCCCTACCGCCCCCCTTCTCACTTCCCCTTCCCCCCTGAGCCGAACTTCT[T/A]GGCCCTGACTCGTGCAGCTTCTGTGGCTAGCACAGAATCCCCCAAAGTCTCACATAAAATGGGGCACGGTCTGGCAGAGACACCCCCAAGCAGTTCTAAGCCTCCCTTCTCCCCAGTAAAGACGTCGCGGCCAGAGCCCCGCAGAGCTCACTCCTGCTCCTCTTCCCCGCTCCTCTTCAACCCTGCCAATGGGAGACCCCTCACCAGCCCTCTTGATGAGCTGAACACTATTTTCAGCTCTGGGCGCAGCCTTCTCCGCAAGTCCACCACAGGAAGAAAGATCAGAGACAGCGGTGAGTGAAAGCCTGTACCTTTAGGTGCAATGTATATTAAAGGTGTTGTAACTCCAGTGCTGTTTGTGGCAACGGTTATTAGACACTTCCCATGTAGTTCAGCCACTAAGGCAAGCAAAGCAATGTTAAAAGCACCACAAAGCAACAATATCTGCACAATGCTTGCAGTTGTCTATAGGCATAGCAAGCTGGCATACAAGAAAGTGT
Associated Phenotype:
Not determined