Busch Lab

ZMP

GIMAP8 (89 of 111)

Ensembl ID:
ENSDARG00000029232
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.
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.
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