Busch Lab

ZMP

LOC100329977

Ensembl ID:
ENSDARG00000060400
Human Orthologue:
GPR12
Human Description:
G protein-coupled receptor 12 [Source:HGNC Symbol;Acc:4466]
Mouse Orthologue:
Gpr12
Mouse Description:
G-protein coupled receptor 12 Gene [Source:MGI Symbol;Acc:MGI:101909]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa16140 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16140
Status:
Available for shipment
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Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085071 Nonsense 308 332 1 1
Genomic Location (Zv9):
Chromosome 21 (position 41968331)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 43567377
GRCz11 21 43562553
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCATCATCAACCCTATGGTATATGCATTYAGGAACCCGGAGATTCTC[C/T]GATCTTTGAGGATTGCTTGTTGTGGRTGCATGCCKTATAGTTTCAGCRTG
Long Flanking Sequence:
ATAACGCATTAACGTACCACACTGAACGCACCATGACGTTCACGTACGTCACGCTAATTTTTATGTGGATCATTAGCGCTGCTCTCGGGTCGCTTCCAGTTTTGGGATGGAACTGTTTGGAGGACGAGAGCACGTGTAGCATTTGTCGACCGGTGAATAAAAACAACGCCGCAGCACTCGCCGTGTCCTTCCTTCTGGTTTTCGCTCTCATTCTGCAGCTCTACCTGCAGATTTGTAAGATCGCTTTCCGACATGCGCAGCAAATCGCAGTTCAGCGCCAGTTCATGACTGCCTCGCATGCATCTTCCACCACGAAAGGAGTTTCAACATTGACCACCATTTTGGGGACTTTTGCGTTCTGCTGGATCCCTCTTGCCATGTATTCGCTGGTGGCGGACACGCGGTCGCCCGTGATTTACACGTACGTCACAGCTCTTCCAGCAATCTGCCACTCCATCATCAACCCTATGGTATATGCATTCAGGAACCCGGAGATTCTC[C/T]GATCTTTGAGGATTGCTTGTTGTGGATGCATGCCGTATAGTTTCAGCGTGCGACCCAGGACACCCAGCGACGTGTAGCAGCGCGTCTTCAGAAGAAAGCACAATCACACTGCGATTAAATGCTTTTTATTAGTCTTGTTTCTAGTCCAAATATCTAAAAATTCTAAAATCTGGTCCTACACCACCCAATCCGCTCTGAGCTGGGATCAAACCAGCGACTTTCCACATGGTAGTCGGTTGCACTACCAAGGAGGCTAAAGATTGGGTCCCACTTTATATTAAGTGGCCTTAACTAATATGTACTTACACATGAATTAATAGTTTGTTACAATGTACTTGTTGTGTAAATACATGTATTTACTGTGTACTTATGCTTGATTAAATACATGTATGTAGTTACATCTGTAATTAACTTCTGTATTTACATTTGTAAATACACTACTGACCATTCCTTACACCTTAACCCACCCTTAAACCTACCCACACCCCCAAACCTGTCCC
Associated Phenotype:
Not determined