Ensembl ID:
Mouse Orthologues:
Gm10891, Gm10893, Gm10909, Gm13896, Gm13926, Gm13979, Gm16591, Gm16837, Gm16940, Gm17015, Gm6037, Gm6683
Mouse Descriptions:
predicted gene 10891 Gene [Source:MGI Symbol;Acc:MGI:3800299]
predicted gene 10893 Gene [Source:MGI Symbol;Acc:MGI:3704436]
predicted gene 10909 Gene [Source:MGI Symbol;Acc:MGI:3642826]
predicted gene 13896 Gene [Source:MGI Symbol;Acc:MGI:3702130]
predicted gene 13926 Gene [Source:MGI Symbol;Acc:MGI:3702147]
predicted gene 13979 Gene [Source:MGI Symbol;Acc:MGI:3651288]
predicted gene 17015 Gene [Source:MGI Symbol;Acc:MGI:4819748]
predicted gene 6037 Gene [Source:MGI Symbol;Acc:MGI:3649172]
predicted gene 6683 Gene [Source:MGI Symbol;Acc:MGI:3704133]
predicted gene, 16591 Gene [Source:MGI Symbol;Acc:MGI:4439369]
predicted gene, 16837 Gene [Source:MGI Symbol;Acc:MGI:4439761]
predicted gene, 16940 Gene [Source:MGI Symbol;Acc:MGI:4439864]


There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa25115 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
We currently estimate that this allele will be available during 2018.
A > T
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113456 Nonsense 63 114 2 3
Genomic Location (Zv9):
Chromosome 2 (position 36203853)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 36500563
GRCz11 2 36483020
KASP Assay ID:
554-7832.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
Flanking Sequence:
Associated Phenotype:
Not determined


If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below: