LOC562936

Ensembl ID:
ENSDARG00000076834
Human Orthologue:
C17orf76
Human Description:
chromosome 17 open reading frame 76 [Source:HGNC Symbol;Acc:32403]
Mouse Orthologue:
BC046404
Mouse Description:
cDNA sequence BC046404 Gene [Source:MGI Symbol;Acc:MGI:2682293]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa19114 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa19114
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 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110618 Nonsense 415 441 4 4
Genomic Location:
Chromosome 15 (position 24087628)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AAGAGGACCTGCAAAGCCAGTCTTCTCATCTGTCTTGCTCTAGCCAGTCA[C/T]AGCACTCATCTGGAGCCATCGAACCTTTAAGAGAAGACTCTGTCCCAGAT
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/yugz6106