ZMP
irgf1
Ensembl ID:
ZFIN ID:
Description:
immunity-related GTPase family, f1 [Source:RefSeq peptide;Acc:NP_001108170]
Human Orthologues:
IRGC, IRGM
Human Descriptions:
immunity-related GTPase family, M [Source:HGNC Symbol;Acc:29597]
immunity-related GTPase family, cinema [Source:HGNC Symbol;Acc:28835]
immunity-related GTPase family, cinema [Source:HGNC Symbol;Acc:28835]
Mouse Orthologues:
9930111J21Rik1, 9930111J21Rik2, AC132320.1, BC023105, Gm12185, Gm4841, Gm4951, Gm5431, Ifi47, Igtp, Iigp1, Irgc1, Irgm1, Irgm2, Tgtp1, Tgtp2
Mouse Descriptions:
RIKEN cDNA 9930111J21 gene 1 Gene [Source:MGI Symbol;Acc:MGI:3041173]
RIKEN cDNA 9930111J21 gene 2 Gene [Source:MGI Symbol;Acc:MGI:3711310]
T-cell specific GTPase 1 Gene [Source:MGI Symbol;Acc:MGI:98734]
T-cell specific GTPase 2 Gene [Source:MGI Symbol;Acc:MGI:3710083]
cDNA sequence BC023105 Pseudogene [Source:MGI Symbol;Acc:MGI:2384767]
immunity-related GTPase family M member 1 Gene [Source:MGI Symbol;Acc:MGI:107567]
immunity-related GTPase family M member 2 Gene [Source:MGI Symbol;Acc:MGI:1926262]
immunity-related GTPase family, cinema 1 Gene [Source:MGI Symbol;Acc:MGI:2685948]
interferon gamma induced GTPase Gene [Source:MGI Symbol;Acc:MGI:107729]
interferon gamma inducible protein 47 Gene [Source:MGI Symbol;Acc:MGI:99448]
interferon inducible GTPase 1 Gene [Source:MGI Symbol;Acc:MGI:1926259]
interferon-inducible GTPase-like [Source:RefSeq peptide;Acc:NP_001094945]
predicted gene 12185 Gene [Source:MGI Symbol;Acc:MGI:3652173]
predicted gene 4841 Gene [Source:MGI Symbol;Acc:MGI:3643814]
predicted gene 4951 Gene [Source:MGI Symbol;Acc:MGI:3644953]
predicted gene 5431 Gene [Source:MGI Symbol;Acc:MGI:3645205]
RIKEN cDNA 9930111J21 gene 2 Gene [Source:MGI Symbol;Acc:MGI:3711310]
T-cell specific GTPase 1 Gene [Source:MGI Symbol;Acc:MGI:98734]
T-cell specific GTPase 2 Gene [Source:MGI Symbol;Acc:MGI:3710083]
cDNA sequence BC023105 Pseudogene [Source:MGI Symbol;Acc:MGI:2384767]
immunity-related GTPase family M member 1 Gene [Source:MGI Symbol;Acc:MGI:107567]
immunity-related GTPase family M member 2 Gene [Source:MGI Symbol;Acc:MGI:1926262]
immunity-related GTPase family, cinema 1 Gene [Source:MGI Symbol;Acc:MGI:2685948]
interferon gamma induced GTPase Gene [Source:MGI Symbol;Acc:MGI:107729]
interferon gamma inducible protein 47 Gene [Source:MGI Symbol;Acc:MGI:99448]
interferon inducible GTPase 1 Gene [Source:MGI Symbol;Acc:MGI:1926259]
interferon-inducible GTPase-like [Source:RefSeq peptide;Acc:NP_001094945]
predicted gene 12185 Gene [Source:MGI Symbol;Acc:MGI:3652173]
predicted gene 4841 Gene [Source:MGI Symbol;Acc:MGI:3643814]
predicted gene 4951 Gene [Source:MGI Symbol;Acc:MGI:3644953]
predicted gene 5431 Gene [Source:MGI Symbol;Acc:MGI:3645205]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7456 | Missense | Mutation detected in F1 DNA | Not yet available |
sa15 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa23522 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7456
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104220 | Missense | 129 | 398 | 2 | 4 |
ENSDART00000134567 | Missense | 129 | 398 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 23784685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 23714100 |
GRCz11 | 19 | 23298423 |
KASP Assay ID:
554-4086.1 (used for ordering genotyping assays)
KASP Sequence:
GCCGATGAGTATCTCGAGTTGGTTGAGTTTGAGCGCTATGATTTTTTCAT[T/G]ATCATCGCTTCAGATAGATTYAGAGAATGCCACACTCAGCTGGCCAAAGW
Long Flanking Sequence:
TGAAACATCCTGTTACGACATCCTGAAAAAAATTTAATAAATCAATGATTTTTTCTCTTATGGCTAGTTTTTATGGCTTTTACCTCTTCAGTTAATAATGAGATTTTTCTTTAGATGGCTACATTTGAAGACTATTGTGTAATAACCCAGGAGGACCTGGATGATATTAAAGATTCAATATCTACACAGGATCTCCCATCAGCTGTAAACACTATAAAAGAGTATCTCAAACAGCAAGATCTCGTTGAACTTAACATTGGTGTGACTGGAGAGTCTGGTTCTGGAAAGTCCACATTTGTCAATGCATTCAGGGGTTTAGGAGATGAAGATGAGGGCTCTGCTGAAACTGGCCCTGTAGAAACCACTATGGAGCCTGAAGTTTATATTCACCCGAAATACCACAATGTGAAAGTGTGGGACCTTCCTGGCATTGGAACACCAAATTTTAAAGCCGATGAGTATCTCGAGTTGGTTGAGTTTGAGCGCTATGATTTTTTCAT[T/G]ATCATCGCTTCAGATAGATTTAGAGAATGCCACACTCAGCTGGCCAAAGAGATCATGAGGATGGGGAAGAAGTTTTACTTTGTTCGCTCCAAGATTGATGCAAGCATTACAGCTGAGAAGAAGAAGAAGAACTTTGACCAGAAAAAGACACTGGATTCCATCCGCAAGGACTGTATAAATGGTTAGTTTATTTGTTTTTTATGAGCAATGTAGAGAAATACATATTGTTTCAAAAATCATTGTATTGAACAAGGCTATTATTCTCATGTAGAAACAGCAATAACTTGAATTATTTTGAGACTTTTGTTTATACATCATCATGACATGTTACTTCTTTAATAGTATATTCTGTCTTTGATAGGTCTGAGAAAGATCGGTATAGAAGATCCCATTGTATTCCTGATCTCAGGCTGGGAGCTCAGCAAGTATGATTTAAATCTGCTGCAGGATAGAATGGAGAAAGAGCTTCCACAGCATAAGAGACGTGTACTGATGTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000104220 | Nonsense | 137 | 398 | 2 | 4 |
ENSDART00000134567 | Nonsense | 137 | 398 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 23784707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 23714122 |
GRCz11 | 19 | 23298445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGTTTGAGCGCTATGATTTTTTCATTATCATCGCTTCAGATAGATTT[A/T]GAGAATGCCACACTCAGCTGGCCAAAGAGATCATGAGGATGGGGAAGAAG
Long Flanking Sequence:
CTGAAAAAAATTTAATAAATCAATGATTTTTTCTCTTATGGCTAGTTTTTATGGCTTTTACCTCTTCAGTTAATAATGAGATTTTTCTTTAGATGGCTACATTTGAAGACTATTGTGTAATAACCCAGGAGGACCTGGATGATATTAAAGATTCAATATCTACACAGGATCTCCCATCAGCTGTAAACACTATAAAAGAGTATCTCAAACAGCAAGATCTCGTTGAACTTAACATTGGTGTGACTGGAGAGTCTGGTTCTGGAAAGTCCACATTTGTCAATGCATTCAGGGGTTTAGGAGATGAAGATGAGGGCTCTGCTGAAACTGGCCCTGTAGAAACCACTATGGAGCCTGAAGTTTATATTCACCCGAAATACCACAATGTGAAAGTGTGGGACCTTCCTGGCATTGGAACACCAAATTTTAAAGCCGATGAGTATCTCGAGTTGGTTGAGTTTGAGCGCTATGATTTTTTCATTATCATCGCTTCAGATAGATTT[A/T]GAGAATGCCACACTCAGCTGGCCAAAGAGATCATGAGGATGGGGAAGAAGTTTTACTTTGTTCGCTCCAAGATTGATGCAAGCATTACAGCTGAGAAGAAGAAGAAGAACTTTGACCAGAAAAAGACACTGGATTCCATCCGCAAGGACTGTATAAATGGTTAGTTTATTTGTTTTTTATGAGCAATGTAGAGAAATACATATTGTTTCAAAAATCATTGTATTGAACAAGGCTATTATTCTCATGTAGAAACAGCAATAACTTGAATTATTTTGAGACTTTTGTTTATACATCATCATGACATGTTACTTCTTTAATAGTATATTCTGTCTTTGATAGGTCTGAGAAAGATCGGTATAGAAGATCCCATTGTATTCCTGATCTCAGGCTGGGAGCTCAGCAAGTATGATTTAAATCTGCTGCAGGATAGAATGGAGAAAGAGCTTCCACAGCATAAGAGACGTGTACTGATGTTGGCTTTGCCAAATATCACACTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23522
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104220 | Nonsense | 207 | 398 | 3 | 4 |
ENSDART00000134567 | Nonsense | 207 | 398 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 23785098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 23714513 |
GRCz11 | 19 | 23298836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAGAAAGATCGGTATAGAAGATCCCATTGTATTCCTGATCTCAGGCT[G/A]GGAGCTCAGCAAGTATGATTTAAATCTGCTGCAGGATAGAATGGAGAAAG
Long Flanking Sequence:
GTGGGACCTTCCTGGCATTGGAACACCAAATTTTAAAGCCGATGAGTATCTCGAGTTGGTTGAGTTTGAGCGCTATGATTTTTTCATTATCATCGCTTCAGATAGATTTAGAGAATGCCACACTCAGCTGGCCAAAGAGATCATGAGGATGGGGAAGAAGTTTTACTTTGTTCGCTCCAAGATTGATGCAAGCATTACAGCTGAGAAGAAGAAGAAGAACTTTGACCAGAAAAAGACACTGGATTCCATCCGCAAGGACTGTATAAATGGTTAGTTTATTTGTTTTTTATGAGCAATGTAGAGAAATACATATTGTTTCAAAAATCATTGTATTGAACAAGGCTATTATTCTCATGTAGAAACAGCAATAACTTGAATTATTTTGAGACTTTTGTTTATACATCATCATGACATGTTACTTCTTTAATAGTATATTCTGTCTTTGATAGGTCTGAGAAAGATCGGTATAGAAGATCCCATTGTATTCCTGATCTCAGGCT[G/A]GGAGCTCAGCAAGTATGATTTAAATCTGCTGCAGGATAGAATGGAGAAAGAGCTTCCACAGCATAAGAGACGTGTACTGATGTTGGCTTTGCCAAATATCACACTGGAGATTAATGAGAAGAAGAAGAAAGCTCTTGAGGAAAACATCAGAAAAGTTGCCTTTCTGTCTGCTTGTGTTGCTCTTTTCCCCCTTCCTGGTCTTTCCATCAGTGCAGATATAGCCATCATAGCAGAAGAGCTGAGAAAGTACTACAGTGCATTTGGTCTGGATGATCCATCCCTGCAGAAACTCTGTGAACGATCAGGGAAAACCGTAGAGGAACTGAAGAGTCTGATGAAGTCTCCTCTGCATCACGGGATCAACCCAAGTTCAATATTAACCTTGCTGGGCGCTGCCTCTGTTCTTATATCAGAAGATGCTGTTGAGTTACTTGTGAGCTTCATACCCATTATTGGCTCTGTGGTGGCAGGAGGACTTTCTTATTTGACCGTCTCAGGAA
Associated Phenotype:
Not determined