ENSDARG00000088112

Ensembl ID:
ENSDARG00000088112
Human Orthologues:
GPR114, GPR56, GPR97
Human Descriptions:
G protein-coupled receptor 114 [Source:HGNC Symbol;Acc:19010]
G protein-coupled receptor 56 [Source:HGNC Symbol;Acc:4512]
G protein-coupled receptor 97 [Source:HGNC Symbol;Acc:13728]
Mouse Orthologues:
Gpr114, Gpr56, Gpr97
Mouse Descriptions:
G protein-coupled receptor 114 Gene [Source:MGI Symbol;Acc:MGI:2685955]
G protein-coupled receptor 56 Gene [Source:MGI Symbol;Acc:MGI:1340051]
G protein-coupled receptor 97 Gene [Source:MGI Symbol;Acc:MGI:1859670]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa21123 Nonsense Mutation detected in F1 DNA During 2014
sa18201 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21123
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:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130064 Nonsense 117 625 3 13
Genomic Location:
Chromosome 7 (position 66765734)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTTCATCTTACAGCAGACACTACAACCAATTGTACTGTGGTTAAATGTTG[G/A]CCGGAAGAAATAAGTAACCTCCTGAAAACGAAAGAAAGTCAAATGGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18201
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130064 Nonsense 551 625 12 13
Genomic Location:
Chromosome 7 (position 66783229)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ATCTTAAAGCTRCATCGTACAAGTAGAAAGTWTGAAAAGATGCCAGTCTG[G/A]AAGGATGCCGGCACAGTGCTGGGGCTCATGTGTCTKCTGGGTACGACATG
Associated Phenotype:
Not determined

Register

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/6vw0ms2n