ZMP
mov10b.1
Ensembl ID:
ZFIN ID:
Description:
Putative helicase mov-10-B.1 [Source:UniProtKB/Swiss-Prot;Acc:Q1LXK4]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41226 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13853 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41228
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 |
---|---|---|---|---|---|
ENSDART00000086946 | Nonsense | 96 | 1013 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 28534107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 27662025 |
GRCz11 | 8 | 27681164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAATTTATAGATTCGAGTGAGGCAAAATGATCAATGGTCCAGACCCTA[T/A]CGCAGCCAACAAAACCATGCTACACCCCATCTTAATGATGCTATTTCACG
Long Flanking Sequence:
GCTGTTTACTGGTTCAACAGGCCTCTCCCAGCTCATACTCCTTTACGACCCCTATTTAAAGCCCCCTCTTCTTGATGGCCCTTATAATGTACATATCTAATATATTCATCACTGTTTTTCCACATACAGTTCGGATTTGGTAATCATGACTAGTGTTCATGTTTTCAAACATCTAAACTGGATACTTCTATTCCATACAGTTTGTGTCTTTTCAATTATACATTTCATGCTTTTCTGACACAGATGGTTCTCATTGTATGCCCAAGTCCTCTCTCGTGCTCTTTTATAACCCATTTGCCTTAACCTGTTACCTGTTTTCAAAGACATATAATGGCAGATTCAAAAGGCCCTCCACTCACCCAATTAATTGTGTTTTCACATAGGTTTAGTAAATAAAATAAATCTTCTTCACATTTGCTTGGAATATCCAGAACATTAACAACCCTATTGTGGAATTTATAGATTCGAGTGAGGCAAAATGATCAATGGTCCAGACCCTA[T/A]CGCAGCCAACAAAACCATGCTACACCCCATCTTAATGATGCTATTTCACGACCATCCACTACCCGTGTTTCAGACCCATCATCAGTTCCAGAGCCAGAAAATAGAGTCATAGCAAGAAGAAGGCTGGCAAAAACCATCATGCGCCAAGGAAACAGCGAAGACATGTAAGGTTGTAACTTTGAACGTTGGATACAAACCATCAAAATGATCAAAACTAACAATGTTTTCCTTCTCAGGTCTGTGTTTTTTGCTGATAAATATGGTGTAAGGGTGTCCTCAGAGCTGCAAATAGAGGATGGCAAGATTCATTGGTGTGTGGAAGGGGCAGAGGTTCATGAGCTAAAGCTGTTTGTGGAGAACACGGGTCAGGAGGCCATACTTTTCACATGTTTCTCTGCTCTTCACTACCTACAGTATTTCACTCTCGACGACAGCCAGAGAGTCAGAAAGGATAATCCACACCGTCTGGAGCCAAGTGAGTCCATTTAAACTGTTTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41227
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086946 | Nonsense | 290 | 1013 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 28533305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 27661223 |
GRCz11 | 8 | 27680362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCACAGGTCCGAGCTCACGGCACAGCTGGGTCCTACAGAACCATTC[A/T]GACCTAAGAGGCTTGACACCAATCAACCAATGAAGTGGAGCATAGATGAG
Long Flanking Sequence:
AGATTCATTGGTGTGTGGAAGGGGCAGAGGTTCATGAGCTAAAGCTGTTTGTGGAGAACACGGGTCAGGAGGCCATACTTTTCACATGTTTCTCTGCTCTTCACTACCTACAGTATTTCACTCTCGACGACAGCCAGAGAGTCAGAAAGGATAATCCACACCGTCTGGAGCCAAGTGAGTCCATTTAAACTGTTTAATACAGGAGAAACTGGTGCTGGTGTTGTTTGGGGCATTCATATGTTAGCATGCTTTTGCCCTTGAACATATTGGGCTTCAGTACTTATGTGAAACAAACTTGTTGTCTTCTCTCTTGATGTTTTAAAGATGAGACATATGAAGTGATCTTGAGATTCAAATCAGATCAGATAGGAGTTTATCCAGCCACTCTGGCGTTTGAGTTCAAGGAAAACCAAGACACCCGTCCTTTCCACATTGTGCGCTTTATTGAGGCACAGCACAGGTCCGAGCTCACGGCACAGCTGGGTCCTACAGAACCATTC[A/T]GACCTAAGAGGCTTGACACCAATCAACCAATGAAGTGGAGCATAGATGAGGGCTTTAAACCTGAAAGGTGAGAGAAATCTCTGCTTGAGTTTTCAGTTCATTTATACACTTCTTTTCTGCTTCATTTGCTATAGCTGTTCATCAGGGCCCGGTTTTTCAAAAGTAATCCACTAGGATTTTGGATAAGGGATTGGATCAAATCTTGAAAATGGGTTTTTCAAAAGAAAAAAACGGATTACATAATCGGATTAGATCACGTAATCCAATCTTGGTTTTGATCCAGATCAAACCTTTTGTAGGAACTCATCGGCATATTACAGTGGTCAACACAAGTTGAATCTGAAATCTTGGGCATCTCCAATGGTCTCATTCATTGAACTAGCTTGAGGGCTTATACCATCAGGATAACAGAGCACCAATTGATTTCGGGCTCCTCTGACCAGTACTTCTCCGCAGATGTTCTAGTACCCTTCGGCTAACTAGCCAATGATTAATTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41226
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 |
---|---|---|---|---|---|
ENSDART00000086946 | Nonsense | 366 | 1013 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 28528444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 27656362 |
GRCz11 | 8 | 27675501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGATTTGTAGGTTAACTCTGGAGAGTGATTTGAGTTTTAATAACTA[T/A]ATGGACCGCTTTGATTTGCTTCTGTACCTGGAGGAGGATCAGATGCGTAT
Long Flanking Sequence:
TTTCTGATGGTATAATAAACTTTGATAAAAATATCACGGTTTCACAGTTTCACGGTATTGAGATTACTGCTCTAAAATAAGTTCTTTTTAAGAAAAAACAACATTATTTTTCACAATTGACCACAATGTATTTTATTTTAGGAAACAATTAAATATATTGGTACTGTAAGCATGTCAGGCTAAATAATTCAAATAAATCATTGACTTCTGCTATGTTTTTTTTTCAGTTTCAGAAACACAGATTTCTTTACAACACATTAAAAAACACATTACAAAACTTACATATACCTTAGGCATGCTATAACAGAAAGTATTAGCGGTTATAAAACATTCACTTTTCCAAACCGTGGTAAACCTTGAAACTGGTTATCGTTCCATACCTATCCAGTAAGAAGTTCTCTGTATGAACATATAGATTAAAAAGCCATTGCTACTGTTTTATTTGTGCATTTGTTGATTTGTAGGTTAACTCTGGAGAGTGATTTGAGTTTTAATAACTA[T/A]ATGGACCGCTTTGATTTGCTTCTGTACCTGGAGGAGGATCAGATGCGTATGGACATCAAGAGATATAACAAAAAGGATGTGTCTATGGTGAGGGATCGAGATAAAAAACTGCTGGTCTTAGAGGTGAGGGGCAGTCTCTTACTGTTTGTTATTAAAGTGTGGGTTAGTGTGTTGGTTCAGACTGCACAATTTTTTTGTCATAGCCATGTGTCATTTTCTGTTCATGTCACAAGAAAAGAGCATAAAAGTCCAAATGCATTCCTATAGTAAATTTAAAAGCAACCGAGTTGTGCCAGAGTGCTTTACAAGAAAAACACAAGAAAAAAACACATGCATCATATGAAAAAAAAGAAAACAATGAAAAAAAAACATTATAAAATTATAATTGACCTTAATCAAAAGCCAGAGAAGACTTGAAAAGATTTGAAAGCAGTATTAAAACTGGCCAGCAAATGTACAAATCTCAGAGGCAAACTATTTCAATTAAATGTAACAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13853
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086946 | Nonsense | 643 | 1013 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 8 (position 28521687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 27649605 |
GRCz11 | 8 | 27668744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGAAGGAGAAAATATTATTTTTCCATGTAAAGAGGAWCTAATGCCCTA[C/A]AAGAKCGTGGTCTGCACTCTGGTMACTGCCGGCAGGTAAAATGCTTTGTC
Long Flanking Sequence:
ATAAAAATACTGTATATTGAAAAAACTATACTTGTAGTGTAATGACAGTGTATTGAAAACTAGTGTACTCAAAGTTAACTATTATTTTACCTAATGTGCTTTTAAAAGTATGCTTTTATAAATGTAAAAGTAAGCCAATTTCCAAGCAGTATTAAAAAAGTATATAAAATATACTTAAATGTATACAGGGTGGGTAACTTATTTAATGACTATCGAACTTGTAGAAATCTTTAACAAATATAATAGTAAATATAGTAATAGGAATATAATAATAAATAGGAATAAATAGGAGTTATTCCCATTTCAACAGTACAGGAATCAGCTGTGAAATGCAGAAATGTTTTATTACCGTTTTAGAATACTTTATTAAATGAACCACACATTTTGAGAAAACAAAGTTGCAAACAATTTTATGTTTAATGTGTTGTTTGTGTTCAGAACAACAGTAATGTGGAAGGAGAAAATATTATTTTTCCATGTAAAGAGGATCTAATGCCCTA[C/A]AAGATCGTGGTCTGCACTCTGGTCACTGCCGGCAGGTAAAATGCTTTGTCTTTCAAACACACTAAAAGCTCACTCTCTCTCGCATACTGTACACATCATAGATAAAGTGCATGCTTGTTGATAGGCTGGTTAGTGGAGGCTTTCCTGTAGGCCATTTTTCTCACATCTTTGTGGATGAAGCTGGTCATGCTGTGGAGCCAGAGATCGTCATCAGTGTGGCAGGTGAAACCCCAAACAATATACAGTAACATCAACACCTAGAGTTTTTTTATTTGAGATAAGTCATTTCTCTGTCTTATCATTGTTTGTAGGACTGCTCAATGCTGAGACTGGACAGCTTGTTCTGGCTGGAGACCCCAAACAACTGGGGCCAATCCTGAGATCTCCCTTTGCCATTAAATATGGACTAGGTGAGATCAGTACATACTTATACAGCAACACATACAGTACACACTCCGTAAACTGTACATTATAATTTGACATGTTTGTAGGTCTTTCAT
Associated Phenotype:
Not determined