ZMP
mov10a
Ensembl ID:
ZFIN ID:
Human Orthologue:
MOV10
Human Description:
Mov10, Moloney leukemia virus 10, homolog (mouse) [Source:HGNC Symbol;Acc:7200]
Mouse Orthologue:
Mov10
Mouse Description:
Moloney leukemia virus 10 Gene [Source:MGI Symbol;Acc:MGI:97054]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40789 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38580 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33959 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11006 | Essential Splice Site | Available for shipment | Available now |
sa18853 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40789
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064826 | Nonsense | 217 | 1001 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 48293206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 48353953 |
GRCz11 | 6 | 48352712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGTGATCAAATAAATACGGCAAATGTTTTCCTGCTAGGTGAGGATTA[T/A]GATGTTGAAGTGCATTACAACGTCAACCATCCCGGACACTTTCCAGCCAC
Long Flanking Sequence:
GCAATGTTAACAACCGTTGAATGCGAACAATGGAACAATGTGAACCCCCCAATGTTGTGTCTTTTATTTTTTGTGTTTGTTTATTATTTCATGTGCAATACTGTAAACTTGTCTAATCTAATGTCAAATGTTCTGTTGTAAAGTTTTAAAAGGTTTTCAATAAAAATAAAGTAATAAAAAAAATTAGGCAAGTTAGGGTAATTAGGCAAGTCATCTTATAACGATGGGTTGTTCTGTAAACAATTAAAAAAACTATTGCTTTACTATTCCTTAAAATGGTTTAAAAGAAAAAAGTTAAACTGCTTTTACTCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGGAGAAAAAATATTATAGGAAATACAGTGAAAAATTCCTTGCTCTGTTAAACATCATTTGGGAAATATTCAAAAAACAAATTCACAGGAGGGCGAATAATTTTGACTTGAGGTGATCAAATAAATACGGCAAATGTTTTCCTGCTAGGTGAGGATTA[T/A]GATGTTGAAGTGCATTACAACGTCAACCATCCCGGACACTTTCCAGCCACCATGTATTTCGAGTTTTGTCCAGAAGTAGATCCTCCGGGTACTGCTAAGCCTTTCTGCATAGTGCGGGAACTGGAGGCGGTGGTTCGGACGGGACTAGCTGAAACGCTGGGTCCGGAGAGCCCATATAACCCTAAACAGAACAGGCGACTCCGTCCAAAGAGCAAGGTGGTGGAGGAAGGGGTACCGCCTGAGAGGTTAGATCTGTCTGTTTATCTGTATATCTATTATCTGTCTGCTTGATTGTCTATCCTTCTGTATGTTTTTCTGTCTGTCCGTCCGTCCGTCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38580
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 |
---|---|---|---|---|---|
ENSDART00000064826 | Essential Splice Site | 346 | 1001 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 48295260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 48356007 |
GRCz11 | 6 | 48354766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCTCTCTCAGTCAGTGTGCATTAGTCAGTGACATGTGTTTGCTCTCA[G/T]GCGACTGCTGGACACTCAGCTCTGCATGAAGAACTACTCTGAGCGCTTTC
Long Flanking Sequence:
ATCCATCCATCCATCCGTATTGTCTGTCTTTCTGTCTATCTATCTATTTGTCTATGTCTATCTGTCTATTTATCTGTCATTCTATCTGTTTGTCTGTCTGTCTGTCTAGCTCATTGTTCCATCTGTAAGTCCATCTGTCACATAGTTCCATCCATCCGTCCATCCAGAATGGATAGATATCTATTTATATCAGTAAGTTTTTTTTAAGTATTGTTTAACCTCTCCTCTCCCCATTATATGTTTATAGCTCCATCACACATGATCTGAAGAATATGATGAAAATGAATCAATATAGGTACCCCGCCTACCTTAAGGAGTTGGCCAAATACAAGCTGGAGGACTCTGAACACCTGCCAGCCTCACTAAAACAGCATCTTCCCAGAGTGAGGCAAGCATGAAATCATTCAGATTGAAGAAGCGGTGTTGAAAATGTTCTGCTGTTTGATGATAGTTTCTCTCTCAGTCAGTGTGCATTAGTCAGTGACATGTGTTTGCTCTCA[G/T]GCGACTGCTGGACACTCAGCTCTGCATGAAGAACTACTCTGAGCGCTTTCACCTCCTCCTACACCTGGAAGAGATTCAGATGGAGGTGGACATCAAGAAATACGACCTGTATGGCAAGACCATGACCCTCGACAAAACAAACAAAAAGCTGCTCATTCTCAAAGTGAGTGACAATAAGAATATAACATTAGTTTTGTTCTTCTTTAGGCCAGATTTTACTGTGAATTACTTCAAAAAAGAAATTCATTACCAATTACTTAATTCAGCATGTATTTATATTTAATTATTTTGTAACTTAACGAAATTTCATGATTTTTAGAAAATTATTAAATTTTTTTATTAAGCAGATACTTGAAAAGTAAGTCCATGGTGTGAAATAAATAGTATAATCTGTTGGTTTTAAATGTACAAAATAATAATGGAAAACCGTTATGTATAAAACCATATTTCATGACTCAATACTTCTTAAATATATTTACATCTGACAATAGATATTTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33959
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064826 | Essential Splice Site | 788 | 1001 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 48307159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 48367906 |
GRCz11 | 6 | 48366665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGATGGAGCGAGAGGCCTTCTGCCAGTGGGAGCATCTCCCTAGAAAGG[T/G]ACCAGACCGCTGTACTAAAGATCTTTTATGAAAATTGTCCAGCCCAGTTT
Long Flanking Sequence:
AGTAAGGAGTTGGATGCAAGCAGAGTATGGCTGTTTGTAAAGTGTACAGCGCCATCTGCTGTTAAAAACTAAGGTCAGAATCGATTCAAGAGAGAATACCGATGCGTTTTAAAAATCTAATTTCCCCACGGCTCTAGTTCATTCCTAACAGATATTTTCATATCTTCTGATGTGAAACAGGTCAGTCCCTTCTGGAGAGGCTGATGAAACGCAACGCTCTCTATCAGAAGAGCCAGGATGATAATTCAAAATACGACAGCCGCTTCGTCACCAAACTTCTGCGAAACTACAGGTACTGATTTGATTTCCTCTACCGTTATTTTTATATGTCGGAAGTGATGATAGGACATTTATTATAGTGTTGTCTTTGCTCTATTGTAGATCTCATCCTGCCATCCTCAAGATACCCAATGAGCTCTTCTATGAGAACGAGCTACAGGTGTTCGCCAACCAGATGGAGCGAGAGGCCTTCTGCCAGTGGGAGCATCTCCCTAGAAAGG[T/G]ACCAGACCGCTGTACTAAAGATCTTTTATGAAAATTGTCCAGCCCAGTTTTAAATAAAAAAAGTGTATGTGTTTAATAGATCGTTACAATTGTTGAAGGGATAGTTCACTCAAAAATTACTCAATAACTCAACCTCAAGTGTTTCCAAACATTTTTTACAGTCGTTTTTTTTGTCTCTTGATCCCAAAAGAAGATAATTTGAAAAATGTTGAAAGCTGGTTACCATTAAAATCCATAGTATGAAAAAAAAGTCTGTGGGAGTCAACAGTTTTGAACATTCTTTAAAATATAATCTGTATTCAACAGACGACATATACTAGAATACATTTGGAACCACTTGGGTAAGAAAATTTGACAATAAAATGTGTATTTTATTTAAGACAATAAAAATTTTTAAGTGAACTGTCTCTTTAATGCAAATATCTAATCATTCAATGGCATTACAGCATTGGTTCCAATATAATTTGTAGTTCTTATTTTTTTCTACATACATTTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11006
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 |
---|---|---|---|---|---|
ENSDART00000064826 | Essential Splice Site | 983 | 1001 | 21 | 22 |
ENSDART00000064826 | Essential Splice Site | 983 | 1001 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 48313771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 48374518 |
GRCz11 | 6 | 48373277 |
KASP Assay ID:
2259-8110.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGAGGATGTGGTCTCACGGCTGGCGTCTTTAAAAATCAGCTCAGATGG[T/C]ACGGAGCATTGCATAACACATCAAGCGTGACTGYATCATATGACTCATTC
Long Flanking Sequence:
ATACCGGTAAATATCTAAAAAATTACGGATTTTTTTCCGGAAAAGACTATTTACACATCCATTCCATAATACCGGTAAATTCTGACATCATTAACCAGAAATGAGCTCTAAACGGCTGGGCTTGTATTTGTAAACATTTGACTACATTTGACCTTTCGAACTATATCATATCTTTAAAATACTACACAGGGATATTTTAGTATTCATAATGTAATTCTAAACTATTTTATTACACTGAAAATGCTCTTAGAAACTCGAGACGTGTTTTATTTTTTTTTTATTCTTTTATCAACTTGAGTGACATTCATGATAAGCAAAGCTAAAATAATTACGATAATATAATAGACGATTAATATCCCACACTCTATATGTGTGTGTTTGTGCAGGTTTATCCAGTACTGTGAGCAGGAGCAGGGCTACACTGGCTTTGACTACAAGGATGCTGAAGGAGAGGAGGATGTGGTCTCACGGCTGGCGTCTTTAAAAATCAGCTCAGATGG[T/C]ACGGAGCATTGCATAACACATCAAGCGTGACTGTATCATATGACTCATTCCAGAACTGCGGATACATTTTCAGGCCAACAAATATTGATATACAACAAATGTGTAATTTGCAGTGAACTCAATCCAATAATAATGAAAAACAATACCATATGGAAGGCGACACGGGGGCTCAGTGGTTAGCACCGTCACCTCACGGCTAGAAGGTCGTTGGTTCGAGACCCGGGTTGGTCAGTTGGCATTTCTGTTTGGAGTTTGCATGTTCTCCCTGTGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCACTATAGGTGAATTGAATAAGCTAAATTGGCCATGGTGTATTTGCGTGAAAGAATGAGTGTTTAGATCAGGGGTGCTCAATCCTGTTCCTGGAGATCTACCTTCCTTTACAGTTTAGCTCCTACCCTGATCAAACCCACCTGAACCAATTAATTAGGACCTGAAATCCACTTGATAATTACAGACAGGTGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18853
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064826 | Essential Splice Site | 983 | 1001 | 21 | 22 |
ENSDART00000064826 | Essential Splice Site | 983 | 1001 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 48313771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 48374518 |
GRCz11 | 6 | 48373277 |
KASP Assay ID:
2259-8110.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGGATGTGGTCTCACGGCTGGCGTCTTTAAAAATCAGCTCAGATGG[T/C]ACGGAGCATTGCATAACACATCAAGCGTGACTGTATCATATGACTCATTC
Long Flanking Sequence:
ATACCGGTAAATATCTAAAAAATTACGGATTTTTTTCCGGAAAAGACTATTTACACATCCATTCCATAATACCGGTAAATTCTGACATCATTAACCAGAAATGAGCTCTAAACGGCTGGGCTTGTATTTGTAAACATTTGACTACATTTGACCTTTCGAACTATATCATATCTTTAAAATACTACACAGGGATATTTTAGTATTCATAATGTAATTCTAAACTATTTTATTACACTGAAAATGCTCTTAGAAACTCGAGACGTGTTTTATTTTTTTTTTATTCTTTTATCAACTTGAGTGACATTCATGATAAGCAAAGCTAAAATAATTACGATAATATAATAGACGATTAATATCCCACACTCTATATGTGTGTGTTTGTGCAGGTTTATCCAGTACTGTGAGCAGGAGCAGGGCTACACTGGCTTTGACTACAAGGATGCTGAAGGAGAGGAGGATGTGGTCTCACGGCTGGCGTCTTTAAAAATCAGCTCAGATGG[T/C]ACGGAGCATTGCATAACACATCAAGCGTGACTGTATCATATGACTCATTCCAGAACTGCGGATACATTTTCAGGCCAACAAATATTGATATACAACAAATGTGTAATTTGCAGTGAACTCAATCCAATAATAATGAAAAACAATACCATATGGAAGGCGACACGGGGGCTCAGTGGTTAGCACCGTCACCTCACGGCTAGAAGGTCGTTGGTTCGAGACCCGGGTTGGTCAGTTGGCATTTCTGTTTGGAGTTTGCATGTTCTCCCTGTGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCACTATAGGTGAATTGAATAAGCTAAATTGGCCATGGTGTATTTGCGTGAAAGAATGAGTGTTTAGATCAGGGGTGCTCAATCCTGTTCCTGGAGATCTACCTTCCTTTACAGTTTAGCTCCTACCCTGATCAAACCCACCTGAACCAATTAATTAGGACCTGAAATCCACTTGATAATTACAGACAGGTGTGTTT
Associated Phenotype:
Not determined