ZMP
GIMAP8 (89 of 111)
Ensembl ID:
Description:
GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:21792]
Human Orthologue:
GIMAP8
Human Description:
GTPase, IMAP family member 8 [Source:HGNC Symbol;Acc:21792]
Mouse Orthologue:
Gimap8
Mouse Description:
GTPase, IMAP family member 8 Gene [Source:MGI Symbol;Acc:MGI:2685303]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6796 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38001 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6796
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104701 | Essential Splice Site | 763 | 839 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 7863974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7427082 |
GRCz11 | 25 | 7601260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTRAAAGTTTTTMAKAATGTCATAATCYGATTTGATTGTATTTCCACA[G/A]TGRGTGGAGATGAGCGCWCYGACAYCTTKTCTCTRGGAAGTTCAGCWTAT
Long Flanking Sequence:
TTTCTGTGTCTAGTTTTACACAAGTAGTAATTTAAAGATTTAGATTTGAAACAAAAATTTTGTTTGATTTGCTTTGATCAGATTTAAATTAGGATTAACAACTGTTCATATATATGTCCACTCATAAAAATAATGTTTTCTTATTGTCACTTATGATTCCACAAAGAACCTAAAATTTAAACTTTTCATTCCCATAAACTTTCTTTATTATTAACTAGATTTTTTTTCTATTTTTAAAATCAGCACATTTTAAAACAGTTGTTCTATGGAATCGGTGTGAATTTTTTTTTGTATTTCTTTATTTTTCCAGACTGTATGATCAACATTAATTACCATATTTCTAAAATTTAGGCAAAACATTTAATTTCATTCTCATCTGGTTGATACATAATTTGTAATGTGTTTTAAAGAGCACCTGATAATGATTAGGCTACATTATTTTAAAGAACATACTAAAAGTTTTTAATAATGTCATAATCCGATTTGATTGTATTTCCACA[G/A]TGGGTGGAGATGAGCGCTCTGACATCTTGTCTCTGGGAAGTTCAGCTTATGGTTCATTCAGATCTCGAACAGGAGACTCAGTTTTTGGATCATCACGCTCCAGAGATTCATCTCACATAGGATTTGTGTCAGGAGCCATTAAACGATATAACAGCATAGATATTCCACCACCAGACTGTGAGTATTTCATTTATTATCAACTGATCTGCTTATACGATGAGCTTACAATATAACTGTTAATTACCAAATTATTTATCTTGCCAGGAAATATAATTGCCAGCAGTTTGCTTAGCGTTTTGTCAACACATTTAAAGTGACTCTTTCTGTATGTGGAAACAGACCATCAAACATGGGTTAAAACATTAAATAAGAATTAGGGTTACATACTAATAATATACATTTATGTACAGCATACATGTAATCTGGAGAGAGACAGGGATAGAGCGATAGAGAAATAGAAAAGTGCGGATTACAATTCAACATCAGTTGCCCAAACAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38001
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 |
---|---|---|---|---|---|
ENSDART00000104701 | Nonsense | 794 | 839 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 25 (position 7864068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7427176 |
GRCz11 | 25 | 7601354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTTATGGTTCATTCAGATCTCGAACAGGAGACTCAGTTTTTGGATCAT[C/A]ACGCTCCAGAGATTCATCTCACATAGGATTTGTGTCAGGAGCCATTAAAC
Long Flanking Sequence:
TTAACAACTGTTCATATATATGTCCACTCATAAAAATAATGTTTTCTTATTGTCACTTATGATTCCACAAAGAACCTAAAATTTAAACTTTTCATTCCCATAAACTTTCTTTATTATTAACTAGATTTTTTTTCTATTTTTAAAATCAGCACATTTTAAAACAGTTGTTCTATGGAATCGGTGTGAATTTTTTTTTGTATTTCTTTATTTTTCCAGACTGTATGATCAACATTAATTACCATATTTCTAAAATTTAGGCAAAACATTTAATTTCATTCTCATCTGGTTGATACATAATTTGTAATGTGTTTTAAAGAGCACCTGATAATGATTAGGCTACATTATTTTAAAGAACATACTAAAAGTTTTTAATAATGTCATAATCCGATTTGATTGTATTTCCACAGTGGGTGGAGATGAGCGCTCTGACATCTTGTCTCTGGGAAGTTCAGCTTATGGTTCATTCAGATCTCGAACAGGAGACTCAGTTTTTGGATCAT[C/A]ACGCTCCAGAGATTCATCTCACATAGGATTTGTGTCAGGAGCCATTAAACGATATAACAGCATAGATATTCCACCACCAGACTGTGAGTATTTCATTTATTATCAACTGATCTGCTTATACGATGAGCTTACAATATAACTGTTAATTACCAAATTATTTATCTTGCCAGGAAATATAATTGCCAGCAGTTTGCTTAGCGTTTTGTCAACACATTTAAAGTGACTCTTTCTGTATGTGGAAACAGACCATCAAACATGGGTTAAAACATTAAATAAGAATTAGGGTTACATACTAATAATATACATTTATGTACAGCATACATGTAATCTGGAGAGAGACAGGGATAGAGCGATAGAGAAATAGAAAAGTGCGGATTACAATTCAACATCAGTTGCCCAAACAGATCATCAAAGAAAACTCAATCGCCTTAATATAACAAAGAAATTCCTGCACTGGCATATCTAATATTTAAATGATACTTGCATTAGGTCTTCTAACT
Associated Phenotype:
Not determined