LOC100334474

Ensembl ID:
ENSDARG00000079292
Human Orthologues:
SAMD9, SAMD9L
Human Descriptions:
sterile alpha motif domain containing 9 [Source:HGNC Symbol;Acc:1348]
sterile alpha motif domain containing 9-like [Source:HGNC Symbol;Acc:1349]
Mouse Orthologue:
Samd9l
Mouse Description:
sterile alpha motif domain containing 9-like Gene [Source:MGI Symbol;Acc:MGI:1343184]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa6877 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa6877
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
ENSDART00000108630 Nonsense 438 954 1 3
Genomic Location:
Chromosome 3 (position 6850978)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CTAACATTCTGCTTACAACWGAKTTATTTTAYGAGTACACTCTGGGAAAA[C/T]AAAAATTAATGCAGGATGTTCACARCATGTTGGTGAGGAGGCAGAATTCA
Associated Phenotype:
Not determined

Register

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* quick link - http://q.sanger.ac.uk/zclhhy8m