ZMP
LOC556241
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 |
---|---|---|---|
sa26940 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34051 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12388 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26940
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 |
---|---|---|---|---|---|
ENSDART00000114919 | Nonsense | 185 | 1509 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 23102430)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 21667615 |
GRCz11 | 7 | 21933953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCAGCATTTCTAAATCTCAGATCTTAAACAAACTGCTTAGCAACCCC[C/T]AACAGTATCATGATACCTTTGTACATCGTGACATGGACTGTGGAGATATC
Long Flanking Sequence:
ACAAGAGTTCAGTGACCGATGAGCCAGCCCAGTTTCTATCATCTTTACCATGGCTACTCCTGAAGAAACTCATGATGGTAAATGTGACGGCAAGAAGTGTCAAATATGCACCAGATGACGATTTGTCAACTTTAGATATCTACAATGACACATCTATTTTTCAGATCGATCAGAATGTCAATGTAAACCCTTTAGACATAGTGACCACCCTCTTTCATTGTTCTGATGGTTTCCTACAACAGGAAATGGTCTCAAAAATGTCAATGTGTCAGTTCTCTGTGCCTTTGCTTCTTCCAGACTGTGATGGTCAACAGTGCATGTACATGCTTTGGGCCATGAGAGATATTGTGAAGAAATTTAGACCTCACTCCTTGTCAGACCAAAAAGGCTTTGTGGAGGACAGAATTGTTCACTCTGAGCTCCCCTTAGTGTCCTTTGTTAGACTGGGTGACTGCAGCATTTCTAAATCTCAGATCTTAAACAAACTGCTTAGCAACCCC[C/T]AACAGTATCATGATACCTTTGTACATCGTGACATGGACTGTGGAGATATCCCGAGAAAGATATCAGATGGGTTAGTGGAGATGAGTTGGTATCTACCTTGTGGAAACAAAAACATTGATGTCTTTCCTGAACCTGTGGCTTTTGCAAACTTGAGAGGGGACATCAGTACCTTTGAAACGCAGTATTCATTCTTATGTCAGACCTCCACTGCAGTTTTTGTGTTTTTTGAAAATCTGGACACAAATTACAAGCTTCTCACCAACCAACATGCTAAAGCACAAGTTTATTTAGTGGGCAACGCCCAAAGCAAAACATTTAATTTGCATCAGCTGAAAAGCACAGCCCTTGAAATGAACTTGAAGAAAGACAACATCATTCTGAAGATGAAACAAAATGATGCACATTTTGTCAAAAATCTGCATACCACAGTGAATTACATAATCAATAACCATCCTATCAAAGCATGCCTGGAGAAAATGGACACCATAGCACACGAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34051
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 |
---|---|---|---|---|---|
ENSDART00000114919 | Nonsense | 481 | 1509 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 23103318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 21668503 |
GRCz11 | 7 | 21934841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGAACCTAGACAATCTCTCCCGAACAAACCTCTCCGACCTCCGAGAG[C/T]AGTACAAAGAAAAGTGTCAGCATTTTTCAGAAAACAAAGAGGAAATCGCA
Long Flanking Sequence:
AACAAAATGATGCACATTTTGTCAAAAATCTGCATACCACAGTGAATTACATAATCAATAACCATCCTATCAAAGCATGCCTGGAGAAAATGGACACCATAGCACACGAGCTTGGAATTCTAGTAGATGAAGACACCGAAGATTGCCAAAAAGCAAAAAATAACGCGCATGTCATAATAAAAGGTATACAGGACACCTTGCAGTTCAAAGAGGATCAGCTTCCCCTTCAGGGTAAAATCTGGAAAGATCTGGCTAAACTGGAAAAAGAGGAATGCAGACTCCGGAAAGCTGGTGATCAAAATATAGAGATATACAAGAGTGATCTCCAGATTAAAAAGATTGAACTCAGGAAACTGCAAAATAAATATGACATTTCAGAGGCAATGTCTTGTTTTATTAGCGCATTATCGACATCAAGCCAGGAGAGGACCTACTTCCTAAAGTGGATGCGGATGAACCTAGACAATCTCTCCCGAACAAACCTCTCCGACCTCCGAGAG[C/T]AGTACAAAGAAAAGTGTCAGCATTTTTCAGAAAACAAAGAGGAAATCGCACAGCTCGATCAACAGATCTCCAACAGTTCTTTAGGAGTAGAGCACTTCCTGCGTGAAATGGGCCAACTTTACGAAGCCGCTGTGTCGCTTTCAGAAAACCTAGAATCACGTCAACAAATGCTCCACTTGCCAAAGTTATGTGCTAAGCTGATGTTGAATGGTTTCCCACTAGAACTGGTTGATGGAGATGCTTCAAATATTCCTCTTAGATGGGTGAGTGATGTACTGAAGTATCTAAACTCTTTAGTGCAGCCCAATAATAAAATCATGGTGGTCACAGTTTTAGGAGTCCAGAGCACAGGGAAATCCACCTTGCTGAACACCATGTTTGGAGTTCAATTTGCTGTCAGCAGTGGAAGATGCACCAGAGGAGCTTTCATGCAGCTGATTAAAGTCAAAGATGACATCAAACAACAACTTGGCTGTGATTATTTAGTGATAATTGACACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12388
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114919 | Nonsense | 549 | 1509 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 23103523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 21668708 |
GRCz11 | 7 | 21935046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCACGTCAACAAATGCTCCACTTGCCAAAGTTATGYGCTAAGCTGATGT[T/A]GAATGGTTTYCCACTRGAACTGGTTGATGGAGATGCYTCAAATATTCCTC
Long Flanking Sequence:
CAAAGAGGATCAGCTTCCCCTTCAGGGTAAAATCTGGAAAGATCTGGCTAAACTGGAAAAAGAGGAATGCAGACTCCGGAAAGCTGGTGATCAAAATATAGAGATATACAAGAGTGATCTCCAGATTAAAAAGATTGAACTCAGGAAACTGCAAAATAAATATGACATTTCAGAGGCAATGTCTTGTTTTATTAGCGCATTATCGACATCAAGCCAGGAGAGGACCTACTTCCTAAAGTGGATGCGGATGAACCTAGACAATCTCTCCCGAACAAACCTCTCCGACCTCCGAGAGCAGTACAAAGAAAAGTGTCAGCATTTTTCAGAAAACAAAGAGGAAATCGCACAGCTCGATCAACAGATCTCCAACAGTTCTTTAGGAGTAGAGCACTTCCTGCGTGAAATGGGCCAACTTTACGAAGCCGCTGTGTCGCTTTCAGAAAACCTAGAATCACGTCAACAAATGCTCCACTTGCCAAAGTTATGTGCTAAGCTGATGT[T/A]GAATGGTTTCCCACTAGAACTGGTTGATGGAGATGCTTCAAATATTCCTCTTAGATGGGTGAGTGATGTACTGAAGTATCTAAACTCTTTAGTGCAGCCCAATAATAAAATCATGGTGGTCACAGTTTTAGGAGTCCAGAGCACAGGGAAATCCACCTTGCTGAACACCATGTTTGGAGTTCAATTTGCTGTCAGCAGTGGAAGATGCACCAGAGGAGCTTTCATGCAGCTGATTAAAGTCAAAGATGACATCAAACAACAACTTGGCTGTGATTATTTAGTGATAATTGACACTGAAGGCCTGAAATCCCCAGAGCTTGCAAAACTAGATGATAGCCATGAACATGACAACGAATTAGCCACACTTGTTGTTGGATTGAGTGACGTCACAATCATCAACATCGCAATGGAGAATTCCACAGAGATGAAGGACATTTTGCAAATTGTGGTCCATGCCTTCCTCAGAATGAAGGAAATAGGTAAAAAACCCAAGTGTCAGT
Associated Phenotype:
Not determined