Ensembl ID:
Human Orthologue:
Mouse Orthologues:
1700042B14Rik, 3110007F17Rik, 4930412D23Rik, 4930428D18Rik, 4930468A15Rik, AL805960.1, Gm16390, Gm2411, Gm4937, Gm5167, Gm6604
Mouse Descriptions:
predicted gene 16390 Gene [Source:MGI Symbol;Acc:MGI:3648403]
predicted gene 2411 Gene [Source:MGI Symbol;Acc:MGI:3809203]
predicted gene 4937 Gene [Source:MGI Symbol;Acc:MGI:3648293]
predicted gene 5167 Gene [Source:MGI Symbol;Acc:MGI:3645501]
predicted gene 6604 Gene [Source:MGI Symbol;Acc:MGI:3644765]
RIKEN cDNA 1700042B14 gene Gene [Source:MGI Symbol;Acc:MGI:1920597]
RIKEN cDNA 3110007F17 gene Gene [Source:MGI Symbol;Acc:MGI:1920311]
RIKEN cDNA 4930412D23 gene Gene [Source:MGI Symbol;Acc:MGI:1921184]
RIKEN cDNA 4930428D18 gene Gene [Source:MGI Symbol;Acc:MGI:3588232]
RIKEN cDNA 4930468A15 gene Gene [Source:MGI Symbol;Acc:MGI:1922237]


There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa8235 Nonsense Mutation detected in F1 DNA During 2015

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 2015.
G > A
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000121492 Nonsense 34 241 1 1
Genomic Location:
Chromosome 6 (position 30154659)
KASP Assay ID:
2259-7669.1 (used for ordering genotyping assays from LGC Genomics)
KASP 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:

* quick link - http://q.sanger.ac.uk/4c9wum1x