Busch Lab

ZMP

GPR125 (2 of 2)

Ensembl ID:
ENSDARG00000073673
Description:
G protein-coupled receptor 125 [Source:HGNC Symbol;Acc:13839]
Human Orthologue:
GPR125
Human Description:
G protein-coupled receptor 125 [Source:HGNC Symbol;Acc:13839]
Mouse Orthologue:
Gpr125
Mouse Description:
G protein-coupled receptor 125 Gene [Source:MGI Symbol;Acc:MGI:1917943]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa34241 Nonsense Available for shipment Available now
sa21149 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa34241
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
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112969 Nonsense 1030 1183 26 27
Genomic Location (Zv9):
Chromosome 7 (position 72819425)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 69817323
GRCz11 7 70267620
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCAGTTCGGTCAACAACAACAATCTTCCAGGCAATGCTAATATTACC[G/T]GACACCCAGGGCGGCATCACAAGAACCGTTCAAGAGCGCATCGGGCTAGC
Long Flanking Sequence:
CAGATTTGGTGTTCGCCTGTTTATTCGGAGCCCTCGCTTTGGGTCTCGGTGCATTTCTTGTTGCGCACCATTGCGTAAACCGACAAGACATGCGACGTCATTGGTCGCAAGCTTGTTGCCTTATTCGTCGCAACTACGCAGTACAAGTTGATTCCCTCCTATTACCGATCGCAGGATCCAGCGGATCAGTAATGACATCCAGAGGAAACGGAGAAGCTACAAAGTGTCCTGCGAGCAGCGCCGAATCCTCCTGCACCAATAAAAGTGCCCCAAGTCTACGCAACTCAACCCAAGGTTGCAAACTAACCAATCTCCAAGTCGAAGCTGCTCAATGCAAAGTAGTAGCACCTTCGACGGCCAATGGGACGGCTGTGTTGGACAACAGCTTGACCGAGCATTCGGTAGACAATGAGATTAAGATGCACGTTGCGCCAATCGAAATCCAATATCGACCCAGTTCGGTCAACAACAACAATCTTCCAGGCAATGCTAATATTACC[G/T]GACACCCAGGGCGGCATCACAAGAACCGTTCAAGAGCGCATCGGGCTAGCAGGCTCACAGTTTTGCGCGAGTACTCGTATGACGTCCCGACTAGCGTAGAAGGAAGCGTGCAAAGCGTCCCAAACAAGAGGCATCATCACGAGAGCCTACACGCTCGTAATAGTCGTCGGGCAGCCTATTTGGCATACCGAGAACGCCAGCAGAGCCAGCTTCAGCAGGACAGCAGTGATGCAGCCAGCACCAGCGTGCCTCGCAGATCGCGACACTTCAGCAAAGGTACCCGCATTGGTAATGGTTTTGGCCACGGGATCAGTAATGGAGGCTTATTGGATGGATCTGAGGCTGATGTCACCAACCAAACTAAAGAGTGTCCAAAACAAACCCTCACTGTTGAGCTGGAGGTACAGCCCAAGTCTTATGGGTTGAATCTAGCATGCCAAAATGGATCTGCCAAAGACTCTGAGAGACTAAATGTTGAGAGTTCGGGGAATGTTAAGACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21149
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112969 Nonsense 1090 1183 26 27
Genomic Location (Zv9):
Chromosome 7 (position 72819244)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 69817142
GRCz11 7 70267439
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCATCACGAGAGCCTACACGCTCGTAATAGTCGTCGGGCAGCCTATT[T/A]GGCATACCGAGAACGCCAGCAGAGCCAGCTTCAGCAGGACAGCAGTGATG
Long Flanking Sequence:
CGGATCAGTAATGACATCCAGAGGAAACGGAGAAGCTACAAAGTGTCCTGCGAGCAGCGCCGAATCCTCCTGCACCAATAAAAGTGCCCCAAGTCTACGCAACTCAACCCAAGGTTGCAAACTAACCAATCTCCAAGTCGAAGCTGCTCAATGCAAAGTAGTAGCACCTTCGACGGCCAATGGGACGGCTGTGTTGGACAACAGCTTGACCGAGCATTCGGTAGACAATGAGATTAAGATGCACGTTGCGCCAATCGAAATCCAATATCGACCCAGTTCGGTCAACAACAACAATCTTCCAGGCAATGCTAATATTACCGGACACCCAGGGCGGCATCACAAGAACCGTTCAAGAGCGCATCGGGCTAGCAGGCTCACAGTTTTGCGCGAGTACTCGTATGACGTCCCGACTAGCGTAGAAGGAAGCGTGCAAAGCGTCCCAAACAAGAGGCATCATCACGAGAGCCTACACGCTCGTAATAGTCGTCGGGCAGCCTATT[T/A]GGCATACCGAGAACGCCAGCAGAGCCAGCTTCAGCAGGACAGCAGTGATGCAGCCAGCACCAGCGTGCCTCGCAGATCGCGACACTTCAGCAAAGGTACCCGCATTGGTAATGGTTTTGGCCACGGGATCAGTAATGGAGGCTTATTGGATGGATCTGAGGCTGATGTCACCAACCAAACTAAAGAGTGTCCAAAACAAACCCTCACTGTTGAGCTGGAGGTACAGCCCAAGTCTTATGGGTTGAATCTAGCATGCCAAAATGGATCTGCCAAAGACTCTGAGAGACTAAATGTTGAGAGTTCGGGGAATGTTAAGACTGGCTTGTGGAAGCATGAAACTACTGTGTAGAGACTGCGAATCAGACTTTTGCCTGTAACTGTGAATTGTTTAATGATGTTAATCCAAATGGTACAGTTTGTAAAAGAATAGTTTTTGAAAGAAATTGCTTTTAAATGTTCAAATTTTGGAGAAAAAAAAATACCTAAGAGTGCGTATAGTT
Associated Phenotype:
Not determined