Busch Lab

ZMP

gpr1

Ensembl ID:
ENSDARG00000063704
ZFIN ID:
ZDB-GENE-091204-457
Human Orthologue:
GPR1
Human Description:
G protein-coupled receptor 1 [Source:HGNC Symbol;Acc:4463]
Mouse Orthologue:
Gpr1
Mouse Description:
G protein-coupled receptor 1 Gene [Source:MGI Symbol;Acc:MGI:2385324]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa14601 Nonsense Available for shipment Available now
sa41331 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14601
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000093341 Nonsense 60 351 1 1
ENSDART00000145580 Nonsense 65 356 3 3
Genomic Location (Zv9):
Chromosome 9 (position 1111533)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 1079024
GRCz11 9 1236656
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTTTGGGSATCATCGGGAACGGGACGGTCATCTGGGTCACCRGCTTC[A/T]AGATCAAACGCAGCATCAACAGCGTCTGGCTCCAGAATCTGGCCATCGCC
Long Flanking Sequence:
GTTTACATGACTTTAGCAACTGTGGCACCTGTCGCCGTATGCTGCCAGAAACTACAGTGAAACACTTGTAAGGATGACAGATAAGAAGTTTGTTGCAACGCTCTAAATAAAATCCCTGAGTTCAATTACTGAAGGACTTTCACGCAAGCGGATACTGGTGTCGACTGTAAATGACGTCACTTCCAGAGTGCAAATCAGCCAGACTCTATTAAAGCCATGACCGAATATAATCATGCTCTGTTGATTGTTGCTGGTTTTCCCTGTTGGGAAGAGGATCCCACTCATGCTTTTTGTCTCCCTCCTGCAGGATGATGACCCAGGATGACATGGACTACGAGAACGACACAGTATACTTCGATGAAACTGGCTATGTGGTTGACAGCCGATCTGGGGGCTACACGCAGCGGGAGGCTTTCCACATCATATCGGTGATCATCTACAGTCTGGCCTTCACTTTGGGCATCATCGGGAACGGGACGGTCATCTGGGTCACCGGCTTC[A/T]AGATCAAACGCAGCATCAACAGCGTCTGGCTCCAGAATCTGGCCATCGCCGACTTCGTCTTCGTCCTCTTCCTTCCCTTCTCCATCGATTACGTCCTGCGGGATTTCCACTGGCTCTTCGGCAAGACCATGTGCAAGCTCAACTCCTTCGTGTGCACCATGAACATGTACGCCAGCATGCTCTTTCTCACGGTTTTGAGCCTAGATCGATATGTGTCTTTCGTGCATTTTAGCTGGTCACAAAAATATCGTAATGTTCGTCGCTCTTGGTGGCTTTGCGCTCTGATTTGGATTATATCCTGCATTTTCAGCTGTCCCGCGCTCGTGTTTCGGGATGTAATCCTTTACAATGGGAAGATCGTGTGCTTTAATCATTTTCACGACGAGGACAGGCATGTGATGAAGATGAGGCATATTGGGATAGTTTCGTTTCGCACTATTGTTGGATTTATTCTCCCGTTTGCTACTATAACAGTAAGTGGGGTCTTACTTGCGCTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41331
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000093341 Nonsense 335 351 1 1
ENSDART00000145580 Nonsense 340 356 3 3
Genomic Location (Zv9):
Chromosome 9 (position 1110707)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 1078198
GRCz11 9 1235830
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTCGCTGCGAGAGCTCAGTCAGTCTGCTTCTGCCACTGAACTGGACT[C/A]GGCTCTGGTCAACTGCGCTCCTGAAGAGCCCGCGGAGAACTCCACTGTCT
Long Flanking Sequence:
GTTTCGGGATGTAATCCTTTACAATGGGAAGATCGTGTGCTTTAATCATTTTCACGACGAGGACAGGCATGTGATGAAGATGAGGCATATTGGGATAGTTTCGTTTCGCACTATTGTTGGATTTATTCTCCCGTTTGCTACTATAACAGTAAGTGGGGTCTTACTTGCGCTTAAAATGCGTCAGTCCAACTCGGTGAGATTATCTAGTTTCTCCAGAATGGTTTCAGCTGTAATTCTGGCTTTTTTTGTGTGCTGGGCGCCCTTTCATACCTTCAGTATAATGGAGTTGAGCGTGCACCACTCCACCGCACTAAACTCAGTGCTCACCATTGGTTTCCCACTGGCCACCAGTCTGGCTTTCTTCAATAGCTGTGTAAATCCCATCCTCTACGTGCTGCTTACTAAGAAAGTGCGTAAACTGGTGAAGAGTGCATGTCTGAAGTTCACCAAGAGCTCGCTGCGAGAGCTCAGTCAGTCTGCTTCTGCCACTGAACTGGACT[C/A]GGCTCTGGTCAACTGCGCTCCTGAAGAGCCCGCGGAGAACTCCACTGTCTGATGGACACCAACGCAACAGGATTTATAGGATGATTCTGGAGCTCAGAATGGACTGAATGAACATGAAAATCTGATTTTATTCCTTATACAGTAAAATGTGCACATTTTATATTTAGGTTTTTAATCAACGCAACAAGCTGCTCGTGTTTTAGATGATGCTTCTGGAGCTCTGATTGGACTGAAACAGATTTCAACATATGAAAATAAGATTTTATTCAACATGAAAATCTGATTTCATTCTTTTTAACAGTGCACTAGTCTTATATGTTGTACAATTTAGGTTTTTAACCCTCGTGTACTGTTCAAATTGACTACCTTTTCGTTATGTTGGGGGCTTTTTTTGCCCCATTGACTTCCATTCCAACCACATTTTTTAATGCACAACCATCACAACAGTAAAAATTCTAAATTGTAGCTCTTCCCGACAGCAAAACCCAACAGCAATCATG
Associated Phenotype:
Not determined