LOC100150280

Ensembl ID:
ENSDARG00000074616
Human Orthologue:
NLRP6
Human Description:
NLR family, pyrin domain containing 6 [Source:HGNC Symbol;Acc:22944]
Mouse Orthologue:
Nlrp6
Mouse Description:
NLR family, pyrin domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:2141990]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa30418 Nonsense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa30418
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 2017.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105198 Nonsense 637 799 4 6
Genomic Location (Zv9):
Chromosome Zv9_NA899 (position 58890)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 71014177
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GTGTCATTGATCTGCAGGTTGAGTGATTGTGGAGTCACAGTTGAAGGTTG[T/A]GCTGCTCTGTCTGCAGCTCTGAGATCGGACTCCTCACCCCTCAGAGAACT
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

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