ZMP
LOC100005729
Ensembl ID:
Mouse Orthologues:
Gm4070, Gvin1
Mouse Descriptions:
GTPase, very large interferon inducible 1 Gene [Source:MGI Symbol;Acc:MGI:1921808]
predicted gene 4070 Gene [Source:MGI Symbol;Acc:MGI:3782245]
predicted gene 4070 Gene [Source:MGI Symbol;Acc:MGI:3782245]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43217 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6143
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053382 | Nonsense | 45 | 1817 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 8311897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7770436 |
GRCz11 | 19 | 7689361 |
KASP Assay ID:
554-3712.1 (used for ordering genotyping assays)
KASP Sequence:
GGGAGCTGCAGGTGTGACTGCAAATAAACAACAAAAATTCCAAGTCGAAT[G/A]GAAGAATGAAGGAATWCACTTTACAAAAACAACAGATGCAAATCATTTTG
Long Flanking Sequence:
CAAATGTAAAATGCATTCAAACAAATATCTACAATTGTAAGCATGTTGGTTAGTGTGTAGGCCAAAGGTGCCCAGATTCAGTCCTGGAGGGCCGGTGTCCTGCAAAGTTTAGTTCCAATTCCAATCAGACACACCTGGGCTAGCTAATCGAGCTCTTACTAGACTTTCTAGAAACATCCGTGCAGGTTTGTCGAGGCAAATTGGAGTTAAAATCTGCAGTACACCGACCCTGCAGGACAGAGTTTGGGCACCTCTGGTGTAGCCCTATAATGCCACACATAAAACACTAAAAAAAGCTGCATGTTTTCTTTTCAACACAGCACAGACCTAAACACAAAGAAAAATCTACAAAAGTAAAAATTGAATTCGTTGTCACTTTTAACTTATATTCCCTTTATCAGATCAAATTAGGATCACAGATGTCGGCCCTCATTCTGTGCGATTAGCATGGGGAGCTGCAGGTGTGACTGCAAATAAACAACAAAAATTCCAAGTCGAAT[G/A]GAAGAATGAAGGAATACACTTTACAAAAACAACAGATGCAAATCATTTTGAGATAAAACAACTCACGCCTGGCACTCGGTATAACATCACGGTACTGGAAACTGAGGAATCCTGCCAGAGCTTCTCTGCATCCGTGTGTACAGGTAAACAAGCTGCTTTCATTTTGTCATGTAAATTCTTTTCTGATACAATCCAAAGAGTATAAATAGGAATTAAATTATAATGATTGCTACACGCTGTAAAAAAATATTCTGTGAAAATTTATTCCTGATATCTTTAATGTTGACTGAGTTAGGCCATGTCATGTGGTGCGGTGGTTTGGTGGTGTTTGACAGAGTGAGTAGAGGTAAATGAGTTGGCAGAGAAGCTGACTTGCTCTGAGAAACGCTGTTGCTGTCGAACATTGTTTACTTCAGAATACTGCAAATACCTGATGGCAACTATGACAAAAATGTTCAAACAGATAAAAATGATCAGATATTTTTTGTCTGAAACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43217
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 |
---|---|---|---|---|---|
ENSDART00000053382 | Nonsense | 700 | 1817 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 8308213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7766752 |
GRCz11 | 19 | 7685677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTACAAGGATGAACTTAGAAGTCGAATACACAAACTGAAAATGGAA[C/T]AAGAAAACAGCAACATGAAACAAGTGATATCTCTGTTCATCTCTGGCTTG
Long Flanking Sequence:
ATTCAAACCAGACACTTCTGAATTCCCTGCAGCTCTCAAAACTGGTACTGGTTTGCAACACAAATGATCTAGAATCAAGAAACGATTTGGAAAAAAGTTTGGCAGAGCTAACGCTCAATACGCACTCAGTTATCTTCAAGGACGTGAAGATGAATGATGATGACTTTGTTGCTAAACTACAGATGACTGTCGATGAAATACTTAAACATTCTACAAGCGTTAGCATCAAAAAAATGTCTGAAATTGCCCCAGATCTGGGGATCCTTGTAGATGAAAATGATGACATTTGTCAAAATGCAAAGAAAATGGCGGAAACAATGACGAAAGACATTGACGATATATCTCAGTTTAAAATAAGACAATTACCTTTGCAAGGGGAAAAGTTGAAAGAGGTTTCCGAACTGGAGAAAGAAATGTGTCGCCTCAGAAAGGCAAAGAAACAAAACATTGAGCACTACAAGGATGAACTTAGAAGTCGAATACACAAACTGAAAATGGAA[C/T]AAGAAAACAGCAACATGAAACAAGTGATATCTCTGTTCATCTCTGGCTTGTGCTGCTCATCAAAATTCCAGATGTATTTTCTTAAATGGATGAAAATAATGTTGGACAGTCTAACAAGACAGCACCTGTCCAGTCTTGATGAGCAGTATAAGGAAGCATGTAAGAAAGCCAGAAAAGAAAAAGAACACCTTAGAAAACTGGAAAATCATATTGCCAACAGCTCTTTAGGGGTTCAACACTTCATGAGAGAATTAAGTCAGCTTTATGAGTCTGCACACTCACATGAAACCTGGAAAAACCCTGCCCTAAAGAACTTACCAAAAGTATGTGCTCAGTTGATGCTGAATGGGTTTCCTCTGGAGCTTGTTGATGGAGAAGCATCGAACATTCCACTGACGTGGATTGGAGATGTGCTTACAGCACTCAACAAACTGACAGCACCTCACAATAAGATCAGAGTCATAACAGTTTTAGGGGTCCAAAGCACTGGGAAGTCTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39228
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053382 | Nonsense | 1773 | 1817 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 8304992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7763531 |
GRCz11 | 19 | 7682456 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGATACAGCCTGACTCTAGTATCGAGGCCACTGACTACTGGAAGTA[C/A]ATCTTTGCCAAGTACAACTCTAAATTTGCTGCACAATACAACGTAAAACC
Long Flanking Sequence:
AAAGAGTTGGTCATACAAACAGACACCCTCAATGCAACTCTAACTTTAAACAACTCTAACCCTGCCGAATTCATAGATTGCTTTAAATCTTCAATAGACAAAATGCATAAGCGATTAGTAGATCAGCTGCACGCTGAAACGAACGCAAGAGATAAACTTACCAGACTCTCTGTGAACAAACCTCAAGAGGTGCTCTTCAACAGAGTGTTTGGCTGTGGAAAAAAGTGTCCGTTCTGCATGGCACCTTGTGAAGCTGGTGGAAAAAGGCATACAAATCACTTTGTGTCCATTCATCGGCCACAAGGCATTGGCTACTATTCCTGGGTCACTAACAATAAACTAATTGCTGACATATGCTCATCTCTAGTCGCAAGTGAAATGACGTTCCGCCATGAAGACACAGGATTTCAGTGGTATCCCTACAAGGAATACAGACAATTCTATCCAAACTGGAGGATACAGCCTGACTCTAGTATCGAGGCCACTGACTACTGGAAGTA[C/A]ATCTTTGCCAAGTACAACTCTAAATTTGCTGCACAATACAACGTAAAACCAGCAGACATTCCTGATAGTTGGTACAGAATCTCTGTACAACAGGCTAACAAATGCTTGGAAGATACATTCAAAATGAAACAATAGAAAGCTACCGATGGACAACATCAATAAATTGTGGAAATGAAACAATGGACAGGTGAACTGGAAAAGTCCACAGAATTCTAAAACTTTTAACATTTTTTTCTTTAGATAACTAGTATTTGCTGAATGGTAGTTCATGAAGAAACAAGCCTTGATGCAACAAATACAGATTTATTAATGTTGTCTATTAAAATATTTTTATAACGAAACAATATATATATATATATATGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAACAATAATATATATATATATATATGTGTGTGTATATAAATATGTTTATATACATATGTA
Associated Phenotype:
Not determined