zgc:152658

Ensembl ID:
ENSDARG00000018587
ZFIN ID:
ZDB-GENE-060929-68
Description:
hypothetical protein LOC767632 [Source:RefSeq peptide;Acc:NP_001070042]
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 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa15254 Nonsense Available for shipment Available now
sa32722 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa15254
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101640 Nonsense 310 339 4 4
Genomic Location (Zv9):
Chromosome 1 (position 40537463)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 39426872
GRCz11 1 40144945
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAGATGAGGCCTATGAAAAAGCACTGCAAACRCTAAACARTAAATATGAG[C/T]AGGTSGCAAGATACAAAGCAGAAATTGACTTCCCAGCAATACTCCATGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32722
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101640 Nonsense 317 339 4 4
Genomic Location (Zv9):
Chromosome 1 (position 40537484)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 39426893
GRCz11 1 40144966
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CACTGCAAACACTAAACAGTAAATATGAGCAGGTCGCAAGATACAAAGCA[G/T]AAATTGACTTCCCAGCAATACTCCATGTGGTCACCACTTTAATTAACGCA
Associated Phenotype:
Not determined

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