ZMP
mxg
Ensembl ID:
ZFIN ID:
Description:
myxovirus (influenza virus) resistance G [Source:RefSeq peptide;Acc:NP_001116443]
Human Orthologues:
AC019294.4, MX1, MX2
Human Descriptions:
Putative UPF0621 protein C [Source:UniProtKB/Swiss-Prot;Acc:A8MV40]
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse) [Source:HGNC Symb
myxovirus (influenza virus) resistance 2 (mouse) [Source:HGNC Symbol;Acc:7533]
myxovirus (influenza virus) resistance 1, interferon-inducible protein p78 (mouse) [Source:HGNC Symb
myxovirus (influenza virus) resistance 2 (mouse) [Source:HGNC Symbol;Acc:7533]
Mouse Orthologues:
Mx1, Mx2
Mouse Descriptions:
myxovirus (influenza virus) resistance 1 Gene [Source:MGI Symbol;Acc:MGI:97243]
myxovirus (influenza virus) resistance 2 Gene [Source:MGI Symbol;Acc:MGI:97244]
myxovirus (influenza virus) resistance 2 Gene [Source:MGI Symbol;Acc:MGI:97244]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24663 | Essential Splice Site | Available for shipment | Available now |
sa24664 | Nonsense | Available for shipment | Available now |
sa7260 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24663
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104340 | Essential Splice Site | 241 | 628 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 20193854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19605831 |
GRCz11 | 25 | 19703782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTAAAACTTGCACAAGAAGTAGATCCTGAGGGCAAAAGAACTATTGG[T/A]AATGTAATACAGAACACCTGTATATAAACACACACGCAAACATTAAATAA
Long Flanking Sequence:
ATCCCCATACGTGGATTAAATCCACCAGAGTGTTATACACTGGGCTTGTATAATGAAATGATGAATAATTTTTTAACTATTGACAGTCCTAAAATAATTCAAAAACTGATGTGTGTTACAGCCCAGGATGAGCTAGCTGGTAATGGGGTAGGAATCTGTGATGAGCTCATCACTTTAGAAGTCATGTCACCCGATGTGTGTAATCTCACATTGATCGATTTACCTGGAATTGCGCGAGTCCCAGTAGCAGGACAACCAGATGATATTGCAAACCAGGTGAGCATTACAACATTATTTTCAAGCCATTTAGGATCATATTTATACAGTAACACGTTCTGTCTTGTTTTTTGTATCCTGTAGATAAAAAAACTGATAATCAAGTTTATTGTGATGCAAGAGACTATTAACCTGGTTGTGGTCCCTTGTAACATTGACATCGCAACAACAGAAGCATTAAAACTTGCACAAGAAGTAGATCCTGAGGGCAAAAGAACTATTGG[T/A]AATGTAATACAGAACACCTGTATATAAACACACACGCAAACATTAAATAACATTATACATACATTTTATGGGTTTAATGCTACACTCTCAGAAATAAAGGTACGCAAACTGTCACCGGGGTGATACCTTTTCAAAAGGTACACATTTGTACTTAAAGGGTCAGTATTGGTACCTCAAAAGTATATATTAGTACCTACAAATTTTAAGAGAAACACTTCTGTACTTTTTAGGTACTAATATGTATCCTTGAGGTATTAATAAGGACCTTTTAGGTACAAATGTGTACCATTTGTAATGGTACCACCCTAGTGACAGCTCACATACCTTTATTTCTGAGAGTGTACACTGAAGTCATGGTTTGGTACGTACATGGCTTTTGGTATCCGGTGCTTTCTCTTTCTGCTTATTTTGAACAGGAAGAAGTGTCTTGCCACAATTAGTTCATAACTAAACAGCTTTTTGTAATGCAAAAGTACAAAATAAATAGAATAATGAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24664
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104340 | Nonsense | 369 | 628 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 20198079)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19610056 |
GRCz11 | 25 | 19708007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATCTAAAAGAGTGTGAGTCTGGACCCCCACAGGATTCAAAAGGGGCC[A/T]AACAATTTCTTATTAAAGTAAGAAGTTTTAATTATCCCATCTAGCAGGAA
Long Flanking Sequence:
CCATCAGATGGCGAAATCGTGCACTGTCAAAAACTTCAAACCATCAATGCAGTTTGATTTAAAAACCTCACTGCTTCAGAAGTTTCATTCTGCACATCCCTACATCATTGTATTATTATGGTGTATTTAGAAAATGGTGTGTTGTTGATTCCCTTGTAGCACATGCAAGTGATTCTGTATAAATGAATGAGTGTTCTAAAGTGAGTCTAGCTCAAACGTTTAGGTACTGTAATATTGTGCTAGGTAAACTTACATAAGGATCCCAAAAATTGGTTAACTTTTGACAACTTCTGACAGTAGAAACTGAAATAACTGAGTGCTGCACTGTACTATACTGTACCACCAAGTGGAAATGAGCCAAAATATGTTTTAATCTTTACCCTACTTTTTTCCAGAAATCGCTGCCACAGCTCAGTGAGCAGATAAAAAAGCAGTTGTGGGACCTGAGAGATGATCTAAAAGAGTGTGAGTCTGGACCCCCACAGGATTCAAAAGGGGCC[A/T]AACAATTTCTTATTAAAGTAAGAAGTTTTAATTATCCCATCTAGCAGGAAAAAAATAGTAGTTGTAATTGTAATTAGAAGTGACTGTGCTTTGCCACAGAAAAACTCTCTGCTGTCTGCTTTAGCTCCAAAGCCTGAGTCCCCTCATGTGTCAGAGCACAGTTACTAATTTACCTTAACTCTGGAGCACATTTCAGATTTTCGAATTCTGCAGCCTCCAAAAGCCTCCTGAGCCCTGTCTTTCTCTTTAAATATGATGCTATTCTGTTGTATTCTGTTGGGTTTCTGTTTTACTCATACCTCCATAATCTGTGCCACCAGCACTGTCCAGCACTCTCCTATGGTTCCTGAATTGACCCTATGCATGGTTACTGTGGGTTTTAGCCAGCTTAGCCCTTTCCTGTGAACCGTCATATCATTTTATATTCACAGCATTTAAGTTCACAGCAATCAATAATTTACACTGCCAGATTGAGACAAAATGTAAAGTGTGTTACATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7260
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 |
---|---|---|---|---|---|
ENSDART00000104340 | Nonsense | 421 | 628 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 25 (position 20200680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 19612657 |
GRCz11 | 25 | 19710608 |
KASP Assay ID:
554-4931.1 (used for ordering genotyping assays)
KASP Sequence:
AAAGTATTSTCTTTTAATAAGAAATGCATATTGTTCTCCAACAAGTAAAA[C/T]AATCAACTAAAGAGAAAATAGAGGTTCTCCAGAATTTCAGAGGGAGAGAA
Long Flanking Sequence:
GTACTTAACAAGATCTAGATCTCTGTTTCTAAACATCGCTTTGTGGTACTATCCGTCGCTTTGAGGCACAAAATTCATCACAAGGACATTTATTATTAATATTTCATCCTGGTGTAATGACTTGGCAAACTACACAAGGAGCTGAGTCTCTGACCACATTAAAAAAAAAAAAAACATCTGAAGGCTCATGTGTTTTAATAAATAGTTAATCATTTAATTGTCCAACAACACTCTCTTGGCTGTGTTTAATCAATATTTTTTGTGCAGATCTTAACAAAGTTTAATGGACAAATCAAGTTATTATCGTCAGGAGAGAAGATGGCTGAGAAAAATTTGTTTGTGCTGCTTCGGGAGGAATTCAATATGTGGAATGATCATCTTAATGAAACAAAGAAGTCCTGTTAGTGTATTTTCAAATAATAAAAAAATATAATACAAGTTCCTAATAAAAAAGTATTCTCTTTTAATAAGAAATGCATATTGTTCTCCAACAAGTAAAA[C/T]AATCAACTAAAGAGAAAATAGAGGTTCTCCAGAATTTCAGAGGGAGAGAACTGCCTGGCTTCAGCAACTACCGAGTGTTTGAGGTGATTTTGCAAAACCATGTGGCCACACTTAAGAACCCAGCATCTAAATTACTGAATGCCATCAAAGGTAACTCATCATGTAATTTCACGTTTAAGATCTTTCTGGTCACCATACTTGTTAACACTGAATAATCAATGAATAATCATGTCAATTTTTTAGTCAAAGTTTGTTAAGTTGCCAGATCTTTCAAACCATTTTTAACCTCAATCTGGCAACCTAAAGCACAGTTGTGCTATTAATTTCTGCGTGGGTAATAGATCTGGGATTTGAATGGCGATGGTAGTAGTGTCAGTGGTAGACAAAGAGAAAAAAATAGATTTTATATAAACAGGGGTTTTACAATGAAACGTAAATGCCTGGTTTTAAACCACAATAATTTATTAGTATAGTGTAGGGCCTCCTTTTGTGGCCAATAC
Associated Phenotype:
Not determined