ZMP
ENSDARG00000077651
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 |
---|---|---|---|
sa30829 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39992 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33092 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33091 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44556 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7549 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30829
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 |
---|---|---|---|---|---|
ENSDART00000111519 | Nonsense | 206 | 2306 | 2 | 5 |
ENSDART00000111519 | Nonsense | 206 | 2306 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8041085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8164517 |
GRCz11 | 3 | 8050357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGAAAGTAGTAAAACGAGCATTACTTGCTGCAGCAATAACCGGAGGAT[C/A]AGGATTAGCAGCACTGGGTATATTTAAAGCAGCAACAGGCCTAGCAGCAG
Long Flanking Sequence:
AAAAACATGGAAACAAACTTCTCTAGACATAACAAAAATGGCACTGACAGTTGCAGTAGTTGCAGTAGCAATACACATAGCAGGAACAAGAGTATTTGACACAGTTGCAGGAGCAGCAGCAGGAGCAGTAGCAGGAGCCGCAGCAGGAGGGGGTATATACATTTTAAGATCATTATGGGAACCAGAAGTGAGACTAATAGAAGAAACAGTGGGAGCAGCAATAGCAACCATAGCAGGAGGTATAGCAGGAACAGCAGCAGCAACACTGCTATCATTAATAGGACAGTCACAGAGAGGATCATCAGTAGTTGGAGCAATAGCAGGAGCTGTAATAGTGGCAGTAATTAGAACATATTTACAACGTGCAACAAGCACAATACTGTGGGCAATATGTAAAGTAAAGCATGTAGTAGCTCTAGTGAACCAAGTAAAATCAGTAGTTCAAAAGGGTATGAAAGTAGTAAAACGAGCATTACTTGCTGCAGCAATAACCGGAGGAT[C/A]AGGATTAGCAGCACTGGGTATATTTAAAGCAGCAACAGGCCTAGCAGCAGCAGGAACAGCAGCAGCAGCAGCAACAACAACAGGAACAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAACAGCAGTGGCAGGAACAGCAGCAGCAGGAACAACTGGAACAGCAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAACAGCAGCAGCAGCAGGAACAGCAGCAGCAACAACAACAGGAACAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAGTAGCAGTGGCAGGAACAGCAGCAGCGGGAACAACTGGAACAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGAAACAACAGCAACAGGGGCAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGAAACAACAGCAACAGGGGCAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGACACAACAGCAACAGGGGCAGCAGCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39992
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 |
---|---|---|---|---|---|
ENSDART00000111519 | Nonsense | 206 | 2306 | 2 | 5 |
ENSDART00000111519 | Nonsense | 206 | 2306 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8041085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8164517 |
GRCz11 | 3 | 8050357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGAAAGTAGTAAAACGAGCATTACTTGCTGCAGCAATAACCGGAGGAT[C/A]AGGATTAGCAGCACTGGGTATATTTAAAGCAGCAACAGGCCTAGCAGCAG
Long Flanking Sequence:
AAAAACATGGAAACAAACTTCTCTAGACATAACAAAAATGGCACTGACAGTTGCAGTAGTTGCAGTAGCAATACACATAGCAGGAACAAGAGTATTTGACACAGTTGCAGGAGCAGCAGCAGGAGCAGTAGCAGGAGCCGCAGCAGGAGGGGGTATATACATTTTAAGATCATTATGGGAACCAGAAGTGAGACTAATAGAAGAAACAGTGGGAGCAGCAATAGCAACCATAGCAGGAGGTATAGCAGGAACAGCAGCAGCAACACTGCTATCATTAATAGGACAGTCACAGAGAGGATCATCAGTAGTTGGAGCAATAGCAGGAGCTGTAATAGTGGCAGTAATTAGAACATATTTACAACGTGCAACAAGCACAATACTGTGGGCAATATGTAAAGTAAAGCATGTAGTAGCTCTAGTGAACCAAGTAAAATCAGTAGTTCAAAAGGGTATGAAAGTAGTAAAACGAGCATTACTTGCTGCAGCAATAACCGGAGGAT[C/A]AGGATTAGCAGCACTGGGTATATTTAAAGCAGCAACAGGCCTAGCAGCAGCAGGAACAGCAGCAGCAGCAGCAACAACAACAGGAACAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAACAGCAGTGGCAGGAACAGCAGCAGCAGGAACAACTGGAACAGCAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAACAGCAGCAGCAGCAGGAACAGCAGCAGCAACAACAACAGGAACAGCAGCAGCAGCAGGAGTAGCAGCAGCAGGAGTAGCAGTGGCAGGAACAGCAGCAGCGGGAACAACTGGAACAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGAAACAACAGCAACAGGGGCAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGAAACAACAGCAACAGGGGCAGCAGCAGCAGGGATAGCAGCAACAGGTATAGCAGCAGCAGACACAACAGCAACAGGGGCAGCAGCAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33092
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 |
---|---|---|---|---|---|
ENSDART00000111519 | Nonsense | 782 | 2306 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8018461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8187141 |
GRCz11 | 3 | 8072981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGGAGCTGGTACAGAGTTTCCTACAAAAACTACTGATGATGAACTA[C/A]AGAGCAAGATACATCAGTACAAAAGAAACCAAAGGACAGGTGCGAATGCA
Long Flanking Sequence:
TAAAGCAAAACTGCAATTGACAAATTTAATTAGGAATGATTTCTAAGCCAAATTTAATATGTAATTAATTAGATTAATTTGATAGTTTAATAGATTAATTTAATAGATGAATAGATAATAGATTAATTAGACAATTTTGATTTTAGCATCAAAATAGTTCAAATTTTAAATGAAAAGCATTAATAATGAAAAAAGGCCTAATTATAAGAACTGAATATGATTCCATGACAATGAAACTGAATAAAATTATCTACTATTTCATCTATTATACAGACAGAAAACGAAGAAAATGGACAAAGAGCACATCAAAACATACAGCAAGAAAAGCCTGAACAAGACAAAAGAGAGCAACTATTTCAGAGACTCCATCTTCACAAAAATGGCAAACTGACAGCTGCACATGTTCTGCAGATATCTGAACATTCTTTAAAGTTACATGAGTCTTGTGCGGAGGAGGAGCTGGTACAGAGTTTCCTACAAAAACTACTGATGATGAACTA[C/A]AGAGCAAGATACATCAGTACAAAAGAAACCAAAGGACAGGTGCGAATGCAGCAAATAGACCAAGAATTGCCTGAAGATGAAGGTGACTTTTTTGATTTTGTTGTGCAAAACAACCATTTGCCAAACACAGGATTAAGTCACTCTGAGAGAATCCACCCGATGGATGTTCAGATGGCTGTGTTTCATTGTGCTGATGCCTTCCTAAAGCAGATGATGGTCATTAAATTGTCCCAGTGTCAGTATGCTCTGCCTCTACTTGTTCCTGATCCAGAAACACAACAGATTGAGTTTCCTCTCTGGACATTCAGACAAATCAACAAGAGTTGGAAAACAAAAAAAGACAATGAAATCATCAGTCAATCCCAGCCAGTCTACAATGCACAAACTCCTATGGTGTTTTTCTTCAGGTATAGCACAGTGTCTCCATCCAAGTCTCATTTGATAAACAGTCTGATCAATGAGAAACACAACACATTCTTCCACAGGAATTGTCCAGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33091
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 |
---|---|---|---|---|---|
ENSDART00000111519 | Nonsense | 1025 | 2306 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8017733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8187869 |
GRCz11 | 3 | 8073709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCCACAACTTCAGAAAAATGACAAAATTACAGCAGAAATCCAGAACT[T/A]GTTTAGAACAGCAAAGCCACTCATTTGCCTTTTTACTGAGGATGAATCTC
Long Flanking Sequence:
GTCCCAGTGTCAGTATGCTCTGCCTCTACTTGTTCCTGATCCAGAAACACAACAGATTGAGTTTCCTCTCTGGACATTCAGACAAATCAACAAGAGTTGGAAAACAAAAAAAGACAATGAAATCATCAGTCAATCCCAGCCAGTCTACAATGCACAAACTCCTATGGTGTTTTTCTTCAGGTATAGCACAGTGTCTCCATCCAAGTCTCATTTGATAAACAGTCTGATCAATGAGAAACACAACACATTCTTCCACAGGAATTGTCCAGGCAGCAGCAGATCTAGAATCCTGATGGATGGAGTGGTGGAGATCGCCTGGTTCTGCCCTTCTGGAAAAGACACTGATAAATTCAATAACTGCGTGGCCTTCTGTAATCTACATGGGGATGCAGGAGAACATGAGAAACAGATGAAGATCCTCACAGAAATGGCCTCAGTCAATGTGGTTCTACTGCCACAACTTCAGAAAAATGACAAAATTACAGCAGAAATCCAGAACT[T/A]GTTTAGAACAGCAAAGCCACTCATTTGCCTTTTTACTGAGGATGAATCTCCCCTAACTGAAATGAAGAAATTTAAGTTCAAAATTGGTTTAAGAAACAGAAATCAGTCAGACATTTCTGAAGAAATACGAAGGGTTATAAATGACTGTCTCTCAGAGTTTTCTTCCATTTTCAGGCCTGTAGATTTATCTAAAGACTCAGACATCAGAGTGGATGAGGAAGACGCTGGAGACTGCATGAGAGGAAGAGCAGCAGCACAGCAGATGATCAGTTTACTTGAAAATGAAAAGCTGACAGAAATCAAAGAATCATTTCTGCCTCATCAGGGGAAACTGTGGCATAAGTGGAGTCTGAAGAACAAAGAACTACATCGACCTCAAGGTTATGAAACAGAAATCGACATCAGTCGAAAACGCACAGAGATAAAGAACATCCGTCAAGAACAACATAAATCTGACATCAGTGATTTTATGAAGCTCTTTATTAATGACATGAGCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44556
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 |
---|---|---|---|---|---|
ENSDART00000111519 | Nonsense | 1919 | 2306 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8015052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8190550 |
GRCz11 | 3 | 8076390 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCATTCAAAAAGCAAACACAACAATCACTGACCAACACGAACTGTTC[A/T]GAGAAGCCAATGATCCTGTCATATATTTTAAGAAGAAGAGAGAAGATTAC
Long Flanking Sequence:
AGAGTGTGACAAAGATTATCAGAGACAATCCAACAGTCAAAGACATTAAGATAATGACTGATGTGAGCGAGATCCTCTGTAACCTCTATAAAAGTGTTTCTGTACAGAAGTACAATAATATTTTTTCTGTGCAGAATTATTCTGATTATGTACAACTGAAAAAATCCAGCGGATTTACAGGACAAATTCAAGATACTTTCAGATCAGTAAAAAAGGGGTTTGGTTTTGATACTCTATCAAAAGAGGGTGAAGCTCAAATAAGATTGTTAGTCAACAATGTTGTTCAGCAGACAGATACAATGATTCAGTCATTTAACATTTCAAAGATGGGTTACAACATCAGCTACATTCAGCAACTCGCAGACTACATCAAGAAGAGAGTAACAGAACATCAAAATGGATCAGTGAAATATGTGTTCAAGAATGAATTCTTCATGGATTTGATATTCTCTATCATTCAAAAAGCAAACACAACAATCACTGACCAACACGAACTGTTC[A/T]GAGAAGCCAATGATCCTGTCATATATTTTAAGAAGAAGAGAGAAGATTACTATAGTATTTTCCAGAAATACTGTCATGGAGCAACATCAGCTGCCATCTTTGGTGAGATCATCTGTCAGAAACTCAAAGAGCCTATTGAGCAGAGCGTCTACAAGAAAACTGCCAGAGAATTAGCTGGTGAAATAAGATCAAACTGTGAATCATTGAATGGAAACAGATCAAATCTGGAGAAACACATCCTGAAGACACTGGCAGAAGAGGAGGACTTTGACAAATACATGAACTACATTACAACTCCCAGAGATCACTTTAAGAGTTTCATCAGAGATGAAGTCAGTCGGTACATCAGTAAAAAGTTCAACATCAGTGTTTTACCTAAGATGAAGAAGAACATTGAACTTCTGCAGCAGAACATCATGAACGCAGCACATGAATCTACAAAACATGCTCAAGTTAATAGTGGAGATGTTGGTTTGTGGCTGAAGAGTTTCACACAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7549
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111519 | Missense | 2237 | 2306 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 8014098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 8191504 |
GRCz11 | 3 | 8077344 |
KASP Assay ID:
554-4153.1 (used for ordering genotyping assays)
KASP Sequence:
TTCCATATAAAGAATACAGAAAAGCAGGAGGACTTTATGCAAAGTGGAGC[A/T]TCACTACTGACCACTCTGAACTGCCCTACTGGAAGTGGTTTGTGTGGAGA
Long Flanking Sequence:
TTAATAGTGGAGATGTTGGTTTGTGGCTGAAGAGTTTCACACAGCAGCTCTCAGAAGATCTGATCTTCTCTGAAAAAGACCTCAGTGGAGTAAATCATGATGATGGTGATGTGAATCTCTTAGAAGATGTGTTAAAACAAGAACTTCCTGATATAATGTCTCAGACCAGCACGGGATTCAACAAGACATTTGGTCAAAAACTGGATGTCAAGTTCAGGCCAGAAGAGCTTCTGATCGATCACTTGTGTCAGTGTTGTTGGGTTCAGTGTCCATTCTGTGGTGCCATCTGCACAAACACCATAGAAAACCATGATGAAGATCACAGTGTTCCTTTCCACAGAGTAGATGGAATTAATGGATGGGAGTACTTTGCAACAAAAAATCTTAGTGTGGATATCTGCACAAATTTAGTTACAAGTGAAAAAACATTTTTTACCAAAGATGGAAAATTTCCATATAAAGAATACAGAAAAGCAGGAGGACTTTATGCAAAGTGGAGC[A/T]TCACTACTGACCACTCTGAACTGCCCTACTGGAAGTGGTTTGTGTGGAGATTTCAGGAAGATCTGGAAAAGAATTACGATGAAAAATTCGAGGAAAATAGTGAGATTCTAACTGAATGGAAAAAAATAACAAAACAGGATGCTACTGAGAGTTTGGAAAAATACATTGGAAGTAGAGACATGCACTCCTGTGGGACAAAATTGGATGGATAAATGCAGGCGTGGGCGGAAAGGTCCTCATGAATGTGCAGGTTGCGGAAGAATACAATTATTGGCAGGACAATTATTTCACTAAAAACAGCTACTCTGATATTTATCTACTGCACAAAGCTGCAGAGAGAGCTTTCAGTGTCTGTGATCACATACTTGAGCAGAGACATATTAATCTGAAGCCCTCATTAGTTAATGACAAATGAATATATGACTACTCCTGCATGGACACATTAAGTATAGGCCCACATTTTTTTTTTAGCTAATTCAGTTTATTTTTATATTAGCTAA
Associated Phenotype:
Not determined