ZMP
ENSDARG00000074748
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 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38366 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33079 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13123 | Nonsense | Available for shipment | Available now |
| sa13108 | Nonsense | Available for shipment | Available now |
| sa39975 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25979 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38366
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 |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 279 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4607168)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4157134 |
| GRCz11 | 3 | 3938951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGAGGATCCTCACTGAGATGGCCTCAGTCAATGTGCTTCTACTTCCA[C/T]AGCTTGATAGAAATGACAAACATGCAACGACAATTCAAAAACTGTACAGT
Long Flanking Sequence:
ATGCTGATGGTTTTCTAAAGCAGCTGATGGTCACTAAACTGTCCCAGTGTCAGTTCGCTCTGCCTCTGCTTGTTCCTGATCCATTCACACAACAGACTGACTTTCCTCTTTGGACATTCAGACAAATCAACAAGAGCTGGAAGATCAGAAACACCAACAATGAAACCATCAGTCAAACCCAGCCCATCTACAAGGCACAAACTCCAATGGTGTTTTTCTTCAGGTTTGACTCTGTGTCTTCATCCAAGTCTCAGCTGATGAACAGTCTGATCAATGACAAACACAACACGTTCTTCCACAGGAACTGCCCAGGCAGCAGCAGATCCAGAGTCCTGATGGATGGAGTGGTGGAGATCGCCTGGTTCTGCCCTTCTGGGAAAAACACAGATACATTTACTGACTGTGTGGCCTTCTGTAATCTACATGGAGATGCAGGAGATCACGAGAAACAGTGGAGGATCCTCACTGAGATGGCCTCAGTCAATGTGCTTCTACTTCCA[C/T]AGCTTGATAGAAATGACAAACATGCAACGACAATTCAAAAACTGTACAGTGACTCAAAGCCACTTATTTGCCTTTTTACTGAAGATGAATCTACTGTTATTCCGACAAAGAAAGGAAAATATAAGATTGGATTAAAAGACAGAAATCAGGCAGATATCTCTAAAGATCTCAGAGGAGCTATAATTAAATGTCTTTTGGAATCATCTTCAACTTTCAGACTTGAAGATGTGTCCAAACACTCAGACATCAGAGTAGATATGGAAGAGGATGAAGACTGCAGGAAAGGAAGAGAAGCAGCACAGCAGATGATCAGTTTACTGCAGAAAGAAAATCTGACAGAAATCAAAGAATCATTTCTGCCTCATCAGGGGAAACTGTGGCATCAGTGGAGTCAGAAGAACAAAGAACTACATCGACTTCGAGGAGATGAGTTAGAAATTGAAATCAGTAGAAAACAAACAGAAATGAAGAAAATCCGTCAACAGCAGCATGAATCTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33079
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 |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 1056 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4609501)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4154801 |
| GRCz11 | 3 | 3936618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAAGTCCTCCTCAGTGATGTCTATAAAAGTGCCTCTTTAGGTCACTG[G/A]AGTGACAGCAGGGACATTTCTATTGAGCAGAACTTTTCTGAATATGTCAT
Long Flanking Sequence:
GAGAGTAAACTACACAACAAAATTGAAAATGAAGCAATTGATGAGATTGAGAAAACTGATCTTCACAATGAACTGAAGGAAACCAGTGAACAAGTGGAAAAATCAATGTCAGATTTTTTTGAGAAGGATCCAGATGCAGATATACTGATTCAGTGGAAAACATCCTTTGAAATAAAAATCCAGGAGATTCAGGAAAACATTGTGAAAGAAACAAAGAGGAAATTAAATGATATTCTTCAGCAACGAGACATGAAGAAAAAGATTGACGCTCAGAGGACACAACATGAAAACACTCTCTATGAAAAGAGTAAAGAACTGGCCTTGAATCTCAAAGACAAAACAAATGATGAAGAAACACTGAAGAAAGAGTTTGAATTATTTTGGGAACAAAGTGTGAAGAAGATCATAAAAGAGACGCCTCCAATCAAAAGCATTGATGTGTTGAAAGATGCAAAAGTCCTCCTCAGTGATGTCTATAAAAGTGCCTCTTTAGGTCACTG[G/A]AGTGACAGCAGGGACATTTCTATTGAGCAGAACTTTTCTGAATATGTCATTTTCACCAAGACCACAAGTAGTGCAGTTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATACGAGCATTAGTCTTAGGGATTGTTGAGGAGACAGAAAGAACGATTCTGTCATCTAACATTTCAAAGATGGGCTACAACAACAGCTACATTCAACAACTTACCAGTGACATCAAGACAAGAGTAACAAAATATCAGGAAGGAGCAGTGAAATATAAGTTCAAGAACGAATTCTTCATTGATTTGGTTTATTCCATGTGTAAAAGAGCAAACAACAAGATCACTGAACAACACAGACTGTTCAGAGAAGCCAATGACCCTGTAATATACATCGAGAAGAAGAAAGAAGAGTACTATAGTATTTTCCAGAAATACTGTCATAGTGCAACATCAGCTGTGATTTTTGGCGAGATCATCTGTCAGAAACTGAAGGAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13123
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 1099 | 1538 | 1 | 3 |
| ENSDART00000099237 | Nonsense | 1099 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4609628)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4154674 |
| GRCz11 | 3 | 3936491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATA[C/T]GAGCATTAGTCTTAGGKATTGTTGAGGAGACAGAAAGAACGATTCTGTCA
Long Flanking Sequence:
ATCCAGATGCAGATATACTGATTCAGTGGAAAACATCCTTTGAAATAAAAATCCAGGAGATTCAGGAAAACATTGTGAAAGAAACAAAGAGGAAATTAAATGATATTCTTCAGCAACGAGACATGAAGAAAAAGATTGACGCTCAGAGGACACAACATGAAAACACTCTCTATGAAAAGAGTAAAGAACTGGCCTTGAATCTCAAAGACAAAACAAATGATGAAGAAACACTGAAGAAAGAGTTTGAATTATTTTGGGAACAAAGTGTGAAGAAGATCATAAAAGAGACGCCTCCAATCAAAAGCATTGATGTGTTGAAAGATGCAAAAGTCCTCCTCAGTGATGTCTATAAAAGTGCCTCTTTAGGTCACTGGAGTGACAGCAGGGACATTTCTATTGAGCAGAACTTTTCTGAATATGTCATTTTCACCAAGACCACAAGTAGTGCAGTTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATA[C/T]GAGCATTAGTCTTAGGGATTGTTGAGGAGACAGAAAGAACGATTCTGTCATCTAACATTTCAAAGATGGGCTACAACAACAGCTACATTCAACAACTTACCAGTGACATCAAGACAAGAGTAACAAAATATCAGGAAGGAGCAGTGAAATATAAGTTCAAGAACGAATTCTTCATTGATTTGGTTTATTCCATGTGTAAAAGAGCAAACAACAAGATCACTGAACAACACAGACTGTTCAGAGAAGCCAATGACCCTGTAATATACATCGAGAAGAAGAAAGAAGAGTACTATAGTATTTTCCAGAAATACTGTCATAGTGCAACATCAGCTGTGATTTTTGGCGAGATCATCTGTCAGAAACTGAAGGAGCCCATTGAAGAGAGCGTCTACAAGAAAACTGCCAGAGATTTAGCAGATGAAATAAAAACAGACTGTGCATCACTGAATGGAAACAGATCAAATCTGGAGAAACACATCCTGAAGACACTGGCAGAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13108
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 1099 | 1538 | 1 | 3 |
| ENSDART00000099237 | Nonsense | 1099 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4609628)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4154674 |
| GRCz11 | 3 | 3936491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATA[C/T]GAGCATTAGTCTTAGGKATTGTTGAGGAGACAGAAAGAACGATTCTGTCA
Long Flanking Sequence:
ATCCAGATGCAGATATACTGATTCAGTGGAAAACATCCTTTGAAATAAAAATCCAGGAGATTCAGGAAAACATTGTGAAAGAAACAAAGAGGAAATTAAATGATATTCTTCAGCAACGAGACATGAAGAAAAAGATTGACGCTCAGAGGACACAACATGAAAACACTCTCTATGAAAAGAGTAAAGAACTGGCCTTGAATCTCAAAGACAAAACAAATGATGAAGAAACACTGAAGAAAGAGTTTGAATTATTTTGGGAACAAAGTGTGAAGAAGATCATAAAAGAGACGCCTCCAATCAAAAGCATTGATGTGTTGAAAGATGCAAAAGTCCTCCTCAGTGATGTCTATAAAAGTGCCTCTTTAGGTCACTGGAGTGACAGCAGGGACATTTCTATTGAGCAGAACTTTTCTGAATATGTCATTTTCACCAAGACCACAAGTAGTGCAGTTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATA[C/T]GAGCATTAGTCTTAGGGATTGTTGAGGAGACAGAAAGAACGATTCTGTCATCTAACATTTCAAAGATGGGCTACAACAACAGCTACATTCAACAACTTACCAGTGACATCAAGACAAGAGTAACAAAATATCAGGAAGGAGCAGTGAAATATAAGTTCAAGAACGAATTCTTCATTGATTTGGTTTATTCCATGTGTAAAAGAGCAAACAACAAGATCACTGAACAACACAGACTGTTCAGAGAAGCCAATGACCCTGTAATATACATCGAGAAGAAGAAAGAAGAGTACTATAGTATTTTCCAGAAATACTGTCATAGTGCAACATCAGCTGTGATTTTTGGCGAGATCATCTGTCAGAAACTGAAGGAGCCCATTGAAGAGAGCGTCTACAAGAAAACTGCCAGAGATTTAGCAGATGAAATAAAAACAGACTGTGCATCACTGAATGGAAACAGATCAAATCTGGAGAAACACATCCTGAAGACACTGGCAGAAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39975
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 |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 1142 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4609759)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4154543 |
| GRCz11 | 3 | 3936360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTACATTCAACAACTTACCAGTGACATCAAGACAAGAGTAACAAAATA[T/A]CAGGAAGGAGCAGTGAAATATAAGTTCAAGAACGAATTCTTCATTGATTT
Long Flanking Sequence:
AAGATTGACGCTCAGAGGACACAACATGAAAACACTCTCTATGAAAAGAGTAAAGAACTGGCCTTGAATCTCAAAGACAAAACAAATGATGAAGAAACACTGAAGAAAGAGTTTGAATTATTTTGGGAACAAAGTGTGAAGAAGATCATAAAAGAGACGCCTCCAATCAAAAGCATTGATGTGTTGAAAGATGCAAAAGTCCTCCTCAGTGATGTCTATAAAAGTGCCTCTTTAGGTCACTGGAGTGACAGCAGGGACATTTCTATTGAGCAGAACTTTTCTGAATATGTCATTTTCACCAAGACCACAAGTAGTGCAGTTGCAGATGTTACAGACCAATCATTGTCTTCAGAGGATGAGACACAAATACGAGCATTAGTCTTAGGGATTGTTGAGGAGACAGAAAGAACGATTCTGTCATCTAACATTTCAAAGATGGGCTACAACAACAGCTACATTCAACAACTTACCAGTGACATCAAGACAAGAGTAACAAAATA[T/A]CAGGAAGGAGCAGTGAAATATAAGTTCAAGAACGAATTCTTCATTGATTTGGTTTATTCCATGTGTAAAAGAGCAAACAACAAGATCACTGAACAACACAGACTGTTCAGAGAAGCCAATGACCCTGTAATATACATCGAGAAGAAGAAAGAAGAGTACTATAGTATTTTCCAGAAATACTGTCATAGTGCAACATCAGCTGTGATTTTTGGCGAGATCATCTGTCAGAAACTGAAGGAGCCCATTGAAGAGAGCGTCTACAAGAAAACTGCCAGAGATTTAGCAGATGAAATAAAAACAGACTGTGCATCACTGAATGGAAACAGATCAAATCTGGAGAAACACATCCTGAAGACACTGGCAGAAGAGGAGGACTTTAAAAAATGTATAAATTACATTCATTATCCCAGAGGTCATTTTAAGAGTTTCATCAGAGATGAAGTCAGTCGCTACATCAGCGATAAGTTCAGCAGCAGTGTTTTACCCAAGATGGAGGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25979
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 |
|---|---|---|---|---|---|
| ENSDART00000099237 | Nonsense | 1337 | 1538 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 4610343)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 4153959 |
| GRCz11 | 3 | 3935776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACATCAATCTACTGAACATGTTCAAGTCAACAGTGGAGATGTTGGTT[T/A]GTGGTTGAAGAGTTTCACACAGCAGCTCTCAGATCAGCTGATCTTCTCTG
Long Flanking Sequence:
GATCACTGAACAACACAGACTGTTCAGAGAAGCCAATGACCCTGTAATATACATCGAGAAGAAGAAAGAAGAGTACTATAGTATTTTCCAGAAATACTGTCATAGTGCAACATCAGCTGTGATTTTTGGCGAGATCATCTGTCAGAAACTGAAGGAGCCCATTGAAGAGAGCGTCTACAAGAAAACTGCCAGAGATTTAGCAGATGAAATAAAAACAGACTGTGCATCACTGAATGGAAACAGATCAAATCTGGAGAAACACATCCTGAAGACACTGGCAGAAGAGGAGGACTTTAAAAAATGTATAAATTACATTCATTATCCCAGAGGTCATTTTAAGAGTTTCATCAGAGATGAAGTCAGTCGCTACATCAGCGATAAGTTCAGCAGCAGTGTTTTACCCAAGATGGAGGAGAACATTAAACTCCTGCAGCAGAAGATCATGAACGCAGCACATCAATCTACTGAACATGTTCAAGTCAACAGTGGAGATGTTGGTT[T/A]GTGGTTGAAGAGTTTCACACAGCAGCTCTCAGATCAGCTGATCTTCTCTGAAAAAGACCTCAGTGGAGTCAAACATGATGATGTTGATGATTTCACACTCCTAGAAGATGTGATCAGACAAGAGCTTCCTGCTGTAATGTCAGACATCAGCAGCAGATTCAACACAGACACATTTCCAGTAAAGCTGGACTATAAGTTCAGGCCAGATGAGCTTCTGATTGATCACTTCTGTCAGTGCTGTTGGGTTCAGTGTCCGTTCTGTAAAGCCATCTGCACAAACACCATGGAGGACCATGAAGGAGATCACAGTGTTCCATTCCATCGTGTAATTGGGATAAATGGGTGGTCTTACGAAGGAACATCAAACTTGTGTACTGACATCTGCACATCAGCAGTAGCAAGTGATAATTATTTTTATCCCAAGCACTCAGATGATGCATATCCCTGCAGAGAATACAGAACAGCGGGAGGGGTTTATGAGAAATGGAGCATCACTCCTG
Associated Phenotype:
Not determined