LOC792520

Ensembl ID:
ENSDARG00000074317
Human Orthologue:
FAM20C
Human Description:
family with sequence similarity 20, member C [Source:HGNC Symbol;Acc:22140]
Mouse Orthologue:
Fam20c
Mouse Description:
family with sequence similarity 20, member C Gene [Source:MGI Symbol;Acc:MGI:2136853]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa38414 Nonsense Mutation detected in F1 DNA During 2016
sa11878 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa38414
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 2016.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113524 Nonsense 138 560 1 10
Genomic Location (Zv9):
Chromosome 3 (position 62557610)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 61660600
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GGACAGCCGGCAGAGGCGCACTGATGTGCGGGTCTCCTCCGTGCTGCAGT[C/A]GCTGTTTGAACATCCGCTCTACCGGACCGTCCTGCCGGATCTAACCGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11878
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113524 Nonsense 438 560 8 10
Genomic Location (Zv9):
Chromosome 3 (position 62621495)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 61724485
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TCTCTCTCTCTGWTTTTGCACTGAACAGGCWACATGGACCGCCATCAYTA[C/A]GAAACTTTYGAGAAGTTTGGAAACGACACTTTCATCATTCATTTGGACAA
Associated Phenotype:
Not determined

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