Busch Lab

ZMP

GIMAP8 (87 of 111)

Ensembl ID:
ENSDARG00000034946
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
sa20003 Nonsense Available for shipment Available now
sa20002 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20003
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103953 Nonsense 37 436 1 4
Genomic Location (Zv9):
Chromosome 3 (position 24967058)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 24545269
GRCz11 3 24675817
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTAGCGTACAACGCTTTTAAATCGGACATGCAGCTGAGCAGAGTTACA[C/T]AATTCTGTGACAAAGCATCTGGAAACATCGGTGGTCGACCTGTGGCCATA
Long Flanking Sequence:
CAAACAGCCTATCGTATATGTAACTGCATTAAATTATTTACTATTCATTTCTTTGCATTTTAACTTTGTAAATTATAAAATCATGTGTCTCCTCAGAGTTTGTATCAGATTTATTTATTTTTTTTAACTTGAGCCCATGAGCCAACTGACTAAAGCCCCTCTTTTTCCCCTGCTCTGCCGGCCAAGCCTCCTCCCTCTGCTGGCAGTGCTCTACACCCATCATGAAGCAGTTTTTTTTTTTAATAAACCGAAAGAGAGGGATTTAAATGTTTGAGTGAAATGAACTCAATTCATTGTAAGAATGTACTGTTCAGTTTCTGTGAAGATTGATCATATTAAACTCTTAATCTGTATTAATCAAAGCATCATTTTTTATGACAGTGTCAGAGGAACTGCGCATCATGTTACTGGGAGCGAGGGGGTCTGGAAAAAGCTCAACAGGAAACACCATCCTAGCGTACAACGCTTTTAAATCGGACATGCAGCTGAGCAGAGTTACA[C/T]AATTCTGTGACAAAGCATCTGGAAACATCGGTGGTCGACCTGTGGCCATAATCGACACGCCGGGACTGAATATAATTGGCAGTACTGAGAAAGAAGTGACCCGAGAGATCCTAAAGTCCATCTCTCTCTATTCTCCAGGACCGCATGTGTTTCTGCTGGTCATGCCTGTGGGGAACTTAACTAATGATGATAAAAGCATGCATAAGCTGATCGAGAGCATGTTTGGGGAGAGAATCTGGCAGTACACGATCATTGTGTTCACTCACGGGGATCGTCTGGAGGGGAAAGCGGCGAATGATGTGATTGCATGTTCAGACATAGAGCTACGCGAATTCATCCATAAATGCAGTGGTGGCTTTCATTTCTTTAACAACAAGGACGATACAAACGACGAGTCTGTTATAGACCTTTTGAAGAAAGTGGAGACTCTGGTAGCCATCAATGGAAAAAGCTGCTACACGTCGTCTTTCTACCCAGCCACAGAGAGGAAGATCAGGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20002
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103953 Nonsense 246 436 4 4
Genomic Location (Zv9):
Chromosome 3 (position 24954964)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 24533175
GRCz11 3 24663723
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAGTGGGAGCAAGAGGATCTGGAAAAAGCTCAACTGGAAACACCATTT[T/A]AAGGTGGAACGCCTTCAACACGGACATGCAGCTGAGCAGGGTCACGCAGT
Long Flanking Sequence:
TGGTCTCGAGAGCTCCCCCTGGTAAAAGGAGGCGATGGGGTAGAAGGAGGGATTCTTGCAAAAGGAAGATAAGGTAGTAAGGCAAAATGGGTCCATTTATTGTACGTTTGAATCAATCTAATTGCATTATTGCTGATTACAGATGAGAGACCAGCTGAGATCAATCATATCACATGCACCTCTCTAAATTAGTTTGTATATCTTTTTTATCATTAAAGTTGTTGCTCTTGACATGTTCCACCCTGTATACCTTACTTTCTTCCTTGGAATACAAAAGAGAAACTTTACATTCCTTAAAAACAAATGTAAACAGGTTTGAACAGATATGAGGATGAGTAAATGATTTAAATATTTGGGTTAACTATTGCTTTAATATTTTCTGCCAAGTTTAAAATCTCAACATACCGTGCATGATCTTCTTCCAGCTGAAGCAGATGAACTGCGCATCATGTTAGTGGGAGCAAGAGGATCTGGAAAAAGCTCAACTGGAAACACCATTT[T/A]AAGGTGGAACGCCTTCAACACGGACATGCAGCTGAGCAGGGTCACGCAGTTCTGTGAAAGAGCAACTGGAAACATCAACGGCCGACCCGTGGTCATAGTAGATACACCGGGACTGAATAAAACCAGTCGAATGGAGAAGGAGGTGACCAGGGAGATCTTAAAATCTGTCTCTCTGTATAAACCAGGACCACACGTGTTTCTGCGGGTTCTGCCGGTGGGGAATTTGACCAATGAGGACAAGGACATGCATAAATTAATCCAAAACATGTTTGGGAAGAGCGTTTGGAATTACACCATTGTTCTGTTCACACATGGAGACCGACTGGAAGGGAAAACACCAAATGATGTGATCGCCAGCTCGGACAAGGATCTTAGAGACTTTATCCGCACGTGCACCGGTGGATTTGTGTTCTTCAATAACAAGAACACTGGCTTTGAGCAGGTCAGCAAACTTCTGGAGAAGATCGACACCTTGGTGGCTGTCAACGGCGGAAGCTGCT
Associated Phenotype:
Not determined