LOC568637

Ensembl ID:
ENSDARG00000079665
Human Orthologue:
GPR158
Human Description:
G protein-coupled receptor 158 [Source:HGNC Symbol;Acc:23689]
Mouse Orthologue:
Gpr158
Mouse Description:
G protein-coupled receptor 158 Gene [Source:MGI Symbol;Acc:MGI:2441697]

Alleles

There are 4 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa11487 Nonsense Available for shipment Available now
sa25775 Nonsense Mutation detected in F1 DNA During 2016
sa9182 Nonsense Mutation detected in F1 DNA During 2016
sa11073 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11487
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113081 Nonsense 59 1286 1 11
ENSDART00000113081 Nonsense 59 1286 1 11
Genomic Location (Zv9):
Chromosome 2 (position 12033826)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12458922
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCGACAAAGATCTCGAAATCAAGGCTAAATATCCTGTTTACAGCACCAGC[G/A]AGACGACGCACCAGCAGCCGACCATCTCCAGCACCGAGCGACCGGCGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25775
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:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113081 Nonsense 59 1286 1 11
ENSDART00000113081 Nonsense 59 1286 1 11
Genomic Location (Zv9):
Chromosome 2 (position 12033826)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12458922
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCGACAAAGATCTCGAAATCAAGGCTAAATATCCTGTTTACAGCACCAGC[G/T]AGACGACGCACCAGCAGCCGACCATCTCCAGCACCGAGCGACCGGCGGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9182
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:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113081 Nonsense 78 1286 1 11
Genomic Location (Zv9):
Chromosome 2 (position 12033769)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12458865
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CGCACCAGCAGCCGACCATCTCCAGCACCGAGCGACCGGCGGTGGCGCAT[A/T]AGCTCGAGGAGGATCTTCCGCGGGTGGTCAYCGCTTTCCTCCACACCGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11073
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113081 Nonsense 254 1286 1 11
Genomic Location (Zv9):
Chromosome 2 (position 12033240)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 12458336
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCGGCTGGTTAAAARTAGAGCGTTTCCAGCAGCGCATGGCGGATATTTTT[T/A]AGRCAAAAGTCATGTCAAGTGGTCTTCGCCTTATCTAGAGTGCGAGCACG
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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