ZMP
si:dkeyp-92c9.3
Ensembl ID:
ZFIN ID:
Description:
myosin-Ig [Source:RefSeq peptide;Acc:NP_001038686]
Human Orthologue:
MYO1G
Human Description:
myosin IG [Source:HGNC Symbol;Acc:13880]
Mouse Orthologue:
Myo1g
Mouse Description:
myosin IG Gene [Source:MGI Symbol;Acc:MGI:1927091]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44915 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43284 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17276 | Nonsense | Available for shipment | Available now |
sa14281 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44915
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 |
---|---|---|---|---|---|
ENSDART00000052418 | Nonsense | 206 | 1010 | 5 | 22 |
ENSDART00000142774 | Nonsense | 206 | 998 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 25223230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 25153342 |
GRCz11 | 19 | 24737565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAGTTGTTCAGCAGCAAGAAGGAGAAAGAAACTTCCATTCATTTTAT[C/T]AGGTGAGACCTTCTTCCAAGTTTTAGTAAATGAGATTGTATGATATTACT
Long Flanking Sequence:
AAAGCAGTTGAAACATTCTTAATATAATTAACAGCATAAAACTCTGTTTTAATGTTTTAATGCTAACTGCTGAAAAAACTATGCTGCTGGTAACGTATGTTTTATGATAGTTTAAGCTGGTTAGTTCTTTGTTGGCCATGTGTTGGTCAGGACCAGCAAAAAAACAGCAAGTACCATCATAAACCAGCAAACAACATATACCTTACCATCAGCATATGCTTTTTTCAGCATGGTAAATATAAGTGTATATAAATACTGTTTTTGGGTGTTCGATTGATGTTATTTTGACTAGCTTTCATTTTTAGGATTTGCTTCCTTTACAAAAAATAACAGAGATTTGTTTTGGCACATTCATCATTACCAATTGTTTACCAATTTTTATTTATTTTTTTAATCAATGTAAGACACAGAAATAACAATTTAATGCAAATACTATGCTGTTTTTACAGTCAAGAGTTGTTCAGCAGCAAGAAGGAGAAAGAAACTTCCATTCATTTTAT[C/T]AGGTGAGACCTTCTTCCAAGTTTTAGTAAATGAGATTGTATGATATTACTCAAAGAGTGCCAAATACTGCGCAAACTGTTTTTACATTATTCAGTATGTAAGTTAATATTCACGTGTTGTGTTTATGCAGTTGTTACGAGGAGGGTCTGATGATTTGCTCAAGTCCTTATATCTACAGAGAGATCCTGCTGAATATACCTACACCAGTCAAGGAGCTTCTGTCACACTTGTAAGTACTTATCAAAAACTACAGTAGTACAGTAGTGTAGTTTATACATGTTTTCAAGACTAAACGTATAGCTTAGTGCTCTTTTTAAAACCAATATTAGTGATGCAAAATGCACAAAATGTTGTTTTTATGTCTTAGTCATTCTTTTTTTCTCCCCTTTGCAAAAATTATCCTCAAAGGCATCCAATAATGACTCCCAATGTCATAAAGCTGTGATGGCAGCATTAAAGGTGATTGGCTTTACTGCTGAAGAAATCAGCTCCATCTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43284
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 |
---|---|---|---|---|---|
ENSDART00000052418 | Nonsense | 209 | 1010 | 6 | 22 |
ENSDART00000142774 | Nonsense | 209 | 998 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 25223093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 25153205 |
GRCz11 | 19 | 24737428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTCAGTATGTAAGTTAATATTCACGTGTTGTGTTTATGCAGTTGTTA[C/T]GAGGAGGGTCTGATGATTTGCTCAAGTCCTTATATCTACAGAGAGATCCT
Long Flanking Sequence:
ATGTGTTGGTCAGGACCAGCAAAAAAACAGCAAGTACCATCATAAACCAGCAAACAACATATACCTTACCATCAGCATATGCTTTTTTCAGCATGGTAAATATAAGTGTATATAAATACTGTTTTTGGGTGTTCGATTGATGTTATTTTGACTAGCTTTCATTTTTAGGATTTGCTTCCTTTACAAAAAATAACAGAGATTTGTTTTGGCACATTCATCATTACCAATTGTTTACCAATTTTTATTTATTTTTTTAATCAATGTAAGACACAGAAATAACAATTTAATGCAAATACTATGCTGTTTTTACAGTCAAGAGTTGTTCAGCAGCAAGAAGGAGAAAGAAACTTCCATTCATTTTATCAGGTGAGACCTTCTTCCAAGTTTTAGTAAATGAGATTGTATGATATTACTCAAAGAGTGCCAAATACTGCGCAAACTGTTTTTACATTATTCAGTATGTAAGTTAATATTCACGTGTTGTGTTTATGCAGTTGTTA[C/T]GAGGAGGGTCTGATGATTTGCTCAAGTCCTTATATCTACAGAGAGATCCTGCTGAATATACCTACACCAGTCAAGGAGCTTCTGTCACACTTGTAAGTACTTATCAAAAACTACAGTAGTACAGTAGTGTAGTTTATACATGTTTTCAAGACTAAACGTATAGCTTAGTGCTCTTTTTAAAACCAATATTAGTGATGCAAAATGCACAAAATGTTGTTTTTATGTCTTAGTCATTCTTTTTTTCTCCCCTTTGCAAAAATTATCCTCAAAGGCATCCAATAATGACTCCCAATGTCATAAAGCTGTGATGGCAGCATTAAAGGTGATTGGCTTTACTGCTGAAGAAATCAGCTCCATCTACAAGACCCTCAGTACCATCCTACACCTGGTCAGTCTCACAACAAATGCTGTGAAATATTGCTTTCTGACATTTTTTCTTTGCCTTTGTAGCTTTTAATTTGATATTTTGGTAAATCAATATTTGCCAAAATTTAAAGCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17276
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052418 | Nonsense | 460 | 1010 | 11 | 22 |
ENSDART00000142774 | Nonsense | 460 | 998 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 25218314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 25148426 |
GRCz11 | 19 | 24732649 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGATTTAGTGGAGCAGCCYCAYAAGGGGATYATCTCYGTTCTGGAT[G/T]AAGCCTRTCTCATTGCAGGGAAAGTCACAGAYACAGTTTGCCTGGACAKC
Long Flanking Sequence:
AAGTCTTTGCTAGCATCTATAACACATTAATAACTTATTGTTAACACTGTTACGAATACATTATTAAAGTATTATTATTTTGTAATATATATTTCAAGATGAACACTAACTACACTGGTTTTATTTAAATATTATCCATATACATATTTTGTCATACATATTAGGCTTCACAGGGTTAATATCACTATAGCTGAAACTGATTGATTTTTCCATTTTCTAACTGCAGTTTTGAACAGTTTTGCATTAACTACTGCAATGAAAAGCTACAGCAGCTCTTCATTGAGCTAATTCTGCGACAGGAGCAGGAGGAGTACCAGAGAGAGGGAATCACGTGGCAACATGTGAGCATAATGCACAAATACATAAAGTAGCACAACTTAATCCAGGTATCTTTTATTTTTAACTGGACTATGGTTTTTCCTCAGATCGAATACTTTAACAATCAGATCATTGTGGATTTAGTGGAGCAGCCTCATAAGGGGATTATCTCTGTTCTGGAT[G/T]AAGCCTGTCTCATTGCAGGGAAAGTCACAGATACAGTTTGCCTGGACAGCATGAACAAAAAGCTGGGCCAGCATCCTCACTACACCTCCCGGAAAGTAAGCACTCACTCTTTCATTATCATTGAGTGTAGTTATAAAGTAACTAGTAACTCTAATAAAACAACTTAACTGTTTTATGTTCAATCCACTTAAATTTGTTAAAAGAATTAAGTTAATTTAATCAATTTGTTTTATGACAATATGAAAGAAATTGTGTGGAACCCAGCATTTTTTACAGTGTAGTTTGTATAAATAGATTTAGAAAAGTTGAGATATATTTAGCAGATTAATTATACACTCGCTGGCCTTTTAATTAGGTACACCTGTCCAACTGCTGTTTAATGTAAATTTCTAATCAGCCAATCACATAGCAGCAACTCAATGAATTCGGGTATGTAGACATGATCAAGATGATCTGCTGCAGTTCATACCGAGCATAAAAATGGCGAAGAAAGGTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14281
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052418 | Essential Splice Site | 540 | 1010 | 13 | 22 |
ENSDART00000142774 | Essential Splice Site | 540 | 998 | 13 | 22 |
Genomic Location (Zv9):
Chromosome 19 (position 25202490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 25132602 |
GRCz11 | 19 | 24716825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACAAGGACCCGCTTTTTCAAGATTTCAAGYGAYTGATGTACAACAGG[T/C]AGTGGTTTTAACCTTTCTTTCAACAAAATAATCAAWATGTCCAAAARAGA
Long Flanking Sequence:
ATAGACAAAAGGGTATTAAAGCCGGTGTCACATCAGCATAGAGATGGCATTTGAATCAGACTGGCATAAAATGGAATCGTGTCACGTCCTGCTCAACCCTCCGCATCACATCCTGTCCTATGTCTGCTCTTGTGTCTATACAAATGTCAAAAAGGTACCCAAATGAATCTTTTAAAACAATCTTTTAATAACCGGCTTCGCTGAAGTAGCCGTCTGAAACATTTAGTTCGTGTCATGCTGTTAAGATAATGGTCCAGGTGTTGGTTTACCTGCCTGCGCTGTGAGTCATCTGTGCTTATGTGATCTGAGTCATAGATGAAGGACTGTTCGCTGAGTGCTTCAGCCTCTGAGTCAGTCAATTAATGCAATTTCCTTGTCCATCTCAAGCCTGGCGCTAATTTCTCTCTTTTCGCTTTCCTCTCAGGTACTCAGTTGATGGCTTTCTTGATAAGAACAAGGACCCGCTTTTTCAAGATTTCAAGCGACTGATGTACAACAGG[T/C]AGTGGTTTTAACCTTTCTTTCAACAAAATAATCAATATGTCCAAAAGAGAACATCCTGTCGTCAGTTATTCTTCATCATGTCTTACACAACCCATAAGGATGTGAAAGAAAAAAAAAACATGTCATTGACGTATGTCATCTACAGTGTATTTGAAACTTAAAGGGATAGTTAAAAAAAAAAAAAGAATAATAACTCAACTTCTAGTTGATGATTTGGCAAAGTGGCAGAAGTAGTTTTTTTCGATGAAATCACAGAAATTAGTCAAGTTTGGTGAAGGAAAAATCATAGTTTGAGCTTACATTCAGTGTGGAGGCATGTGGGACATCTGTAGAGTAGATGACAACATCAACAGCCTGAGGTATCAAGACATTTGTGCCGCCCATTACATTACAAACCACAGGAGAGGGCAAATTCTTCAGCAGCATAGCTTCTCATACTTCAGCCTCCACATCAAAGTTGCTGAAAGCAAAGGAGGTCAAGGTGCTCAGGTATTGGCCTG
Associated Phenotype:
Not determined