Busch Lab

ZMP

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 4 alleles of this gene:

Allele Name Consequence Status Availability
sa21123 Nonsense Available for shipment Available now
sa34226 Nonsense Mutation detected in F1 DNA Not yet available
sa18201 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21123
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130064 Nonsense 117 625 3 13
Genomic Location (Zv9):
Chromosome 7 (position 66765734)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64680808
GRCz11 2 28402805
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCATCTTACAGCAGACACTACAACCAATTGTACTGTGGTTAAATGTTG[G/A]CCGGAAGAAATAAGTAACCTCCTGAAAACGAAAGAAAGTCAAATGGTTTT
Long Flanking Sequence:
TCCAGGAACAAGTTTGGTGACCCCTGCCCTACAGTATAAATAATTTTTCACAAACTTACATTGCCCTGTATAATTCTGTGTAATTTGTGTTTGCCAGGAAATGTTACACTGCAAAATTACCAAACAGTAATACATATTGATATCTCACTGAACTCTGGACACCGCATTACTATTGAGGACGGAGTAAATAAATTACAGTGTAATTACAGTTCATTAACAATCCCATGTTATGCTGAGTGCTCCCATAACAACTTTGTAAACAAAAACTTGACCGACCCACAACAAAGTCAAATATTTGTGACGGATAACTATAAGAACTACACTACAATAAGATTCACCATACGTAAGACTTCTTTTCTTCCATTGCATCTAACCAGCTAAACAACAGCATTTGTGACAAATGTGCAACTGAGAATAATGATTTGATTCACTCATGACAACATGTTTTCCTTTCATCTTACAGCAGACACTACAACCAATTGTACTGTGGTTAAATGTTG[G/A]CCGGAAGAAATAAGTAACCTCCTGAAAACGAAAGAAAGTCAAATGGTTTTCCCGAAAGACGTGAAAAACATTAACAATGTTAAAAACATGTGTGGAGCTGTGATCTTAAACGAAACTGTGACGGACACCTACATTAGGTAAAAGTATTGTTGTTAAGTATTTTAAAGTGCACAGTTCTTTAGTTAAGTGCTTCAAAGCTTGTTTCTGGTGGCTTCTACCTTCCTTATCTGACGCAATTAAATGTACAGTTCCCGGTAAAGTCTAGATCGGATACACGGCTGGCTGGATATGCGATATACACATCAATATAGCAGCATTTTGTATGACACTGTATGACAATAATAATTATGTTTATAGTACTGTGATGGTTGGGTTTAGGCTTGGGGTGGGGGTAGACATTAAAAATACAATTTATTGGGTAATTTAATAGATGGCATAAATAATACTCGGTACAACTACTGTTTTTACGTTACTGTGGCCGTTGGGTTTAGGGTTGGGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34226
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130064 Nonsense 491 625 11 13
Genomic Location (Zv9):
Chromosome 7 (position 66782248)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64697322
GRCz11 2 28386291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTCAGTTCATAACATCAGACCCTTTTATGGCACCCATGAGATGACAT[T/G]AACAGACACTGATCGGACCAATTCAATGTAAGTCTTCACATTACATTATT
Long Flanking Sequence:
ACAACTAATAATTTTTTGACAATCCTATTTGCTGAAATATTAAAAGAAAAACTTCACGATGGTGTTACCAAGACTTTCAGATAAAGGAAAAAAATCGTGTGAGACTAATAACGGCAGCCAGAAGAGAGGATAATGTCAAATTTGCTGGCCTGCCCCATTGGCACTGCATTAGAAACACAACAAGAAAACACACAAAAGATGATACAATACATACGTAAATACATAAACTGCAAATGCATTTTCTTTAATCTAAATATTAAAAACTTAAGGGTTTAAGATTACGTTGACCGTTAAACATGTCATAAAAGTCTTGTGAAAATGGTCCATTGAAAATATGATTTAAAAAATAATTATAATACAAAACTATCAAATTCGAACCTTGAAATGTGGTGATTTATCTTGGAATAATTTATCATTGACAGGAGTCCCTGCTGTTGTTGTTGGAGGCTTGCTGTCAGTTCATAACATCAGACCCTTTTATGGCACCCATGAGATGACAT[T/G]AACAGACACTGATCGGACCAATTCAATGTAAGTCTTCACATTACATTATTCACATTACTTCACAGCTAATGTCACTCAGAGTATAAATAATTTACGAATATTTTCCGGATGGACTGTAAACAGACCAATTTTAACCTACTTTTAACCTACTGTCGTATCTTCGATTTGGAAGAATCTCCCCTTCCACCCCATCTCCTCCTTTTCCTTCTTTACTAGAGGGAATTCTCGCCACCTACCTGATCTCAAACCCCCTTATATATTAAAAGACCAGGCGGAAGCCCTGGGCTCAATTATCTCTGAGCTCTGGGACAACATGTCAAACCTGCTAAGAGCGTCAAGCAATATCTAAGTGTGAACTCTTGAAAATGTAATACGCTAAAGTATAACCACTCACTCATGAATTTCATTTACTCATTCATTTTGCTTTGGCTTAATTTGGCTTAGTCTATGTTTCAGAGGTCGCCTCAATGGAATGAACCACCAACTATGCCAGCATATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18201
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130064 Nonsense 551 625 12 13
Genomic Location (Zv9):
Chromosome 7 (position 66783229)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 64698303
GRCz11 2 28385310
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTTAAAGCTRCATCGTACAAGTAGAAAGTWTGAAAAGATGCCAGTCTG[G/A]AAGGATGCCGGCACAGTGCTGGGGCTCATGTGTCTKCTGGGTACGACATG
Long Flanking Sequence:
CCAACTATGCCAGCATATGTTTAAACATGTTTTTATGTTTTTTTTTATGGCCTTCCAGGTGCAACCTAGTGCTGAGAAACAACCATATGCACATATTCACACACACACTCATACACATTCATTCATTTTCTTGTCCGCTTAGTCCCTTTATTAATTCGGAGTCGCCACAGTGGAATGAACCGTCAACTTATCCAGCAAGTTTTAACGCAGCGGATGCCCTTCCAGCCACAACCCATCTCTGTAAAACATCCACACACACACTCATACACTACTGACAATTTAGCCGACCCAATTAACCCATGTCAACAGTACAATTTACTTACAATGCAAATCTTTCTTTCATTCAGCTGCTGGATCAAAGAGAACATCATCCTGTACGGCGTGACCCTTTCCTACTTCAGTATCGTATTCCTGTTCAACTTAGGAATCCTGATCACAGTGTCTAGACAGATCTTAAAGCTACATCGTACAAGTAGAAAGTATGAAAAGATGCCAGTCTG[G/A]AAGGATGCCGGCACAGTGCTGGGGCTCATGTGTCTGCTGGGTACGACATGGGGTTTGGCCTTCTTCACCTCTGGACATACCATCTACCCTATACTCTACCTATTCTGCATCTTCAACTCAATGCAAGGTGGGTGCCACAAGATACTAACCGAGACTCTCACACAATGTACTGTAGACTTTAAATCCATAAAATGACAATAGCACAAATAAGGTAAAAATGTATCCATTTTAACCAGGGATGCGCCTTTACCTCAATTTTTTTAGCCAATTTAAATTGCTGATTCTTGGCCAAGCAAATTTACATGTATTTAGTCTTTTAAAAAAGAAATAGATAAATATAGTAAGAAATAAAGTAAAAGTGTGTAATGTTAAAACAGGGGTCTTTTCTTCATACGTGGATTAATCAATTAGCTGGATTTAGTTATTGAATCGCCGGCAGCTAGCTCTCTGCAATTTTCACATGGTCGCCCACTGAAGCTAAGCAGGGCTGCGCCCGGTCA
Associated Phenotype:
Not determined