ZMP
si:dkey-32o22.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
GPR156
Human Description:
G protein-coupled receptor 156 [Source:HGNC Symbol;Acc:20844]
Mouse Orthologue:
Gpr156
Mouse Description:
G protein-coupled receptor 156 Gene [Source:MGI Symbol;Acc:MGI:2653880]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10879 | Nonsense | Available for shipment | Available now |
sa25418 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34566 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10879
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128704 | Nonsense | 460 | 800 | 9 | 9 |
ENSDART00000139138 | None | None | 161 | None | 4 |
ENSDART00000147378 | None | None | 136 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 9901934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9702485 |
GRCz11 | 9 | 9680522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCCACCTCCCTATGTACCTCCTCCACCAATTCCCATCCAYACTACCT[C/A]AARTGCAAMATCCCCTGAAGGTCCAGGAGCTACAGATRAGTCTTCACCAY
Long Flanking Sequence:
CGATGATAAATTCCAGTGTTGGGTGGGATAGCAGTGTGTTTTGCGTCACTAACCTACAAGTAAGGCTGGAGCCTTTGTTTTACATTTCCTTAAGGCACTGCTTTGTGATCTCACATCCTGTTAAATTGGCACCTAACCCATTCATCTACTTAGTGAAATGAGCCATTCTAGATAATAACAGTGATTAAAGTGATGAGTTTAAACCATTTTCCCCATGTGTCCTCCATATTTGCAGAAAAATGCAGTTATTGATAGCCTACAGGAACAAGTGAACAATGCCAAGGATAAGCTGCTCAAACTGATGACTGCTAGCCAGCTCTTGGATGAGAGAGAAATGGACTCGTCCAACACTAACCTCAACTCCACCTCCACCCAAACCACAGTGGTATCTCCCGATTCTCCAACACTTGTTCTAAAACAATACTCAGAAGTCGCTCCCACCAGAGTTCTCTCTCCACCTCCCTATGTACCTCCTCCACCAATTCCCATCCACACTACCT[C/A]AAATGCAACATCCCCTGAAGGTCCAGGAGCTACAGATGAGTCTTCACCACACCTGAGGACACAAGGTAACTCTTTCCTTGAAGTTGAAAGCCTAAAAGGAAACACAGAAGACAATATCAGATACTCCGGTCTTGGAAAAGAAATCTCTGAGAAACCACAAGATGTGCCTTTGGATCAGGAAAAATTAACTGAGGATTTTCCTCCTCCAGCTTCTACTCAGTTTAATTTACCTCAGGTTGAGTCTCCAGTGCCTTCAGCCTCTGTTGAGCTCCCTGCCATTTCCCCAGCAGGTAGACTGGGCTTTGTGACCAATGAGCAGCTGGTGGAGATCTTGCAGGATCTGAGTATAGATGCTGTAAGCAGCTCTGTCAAATCACCCGACAGGGCGAGGAGCCCATCTATCAATCCAGATGAACTAAGCATGACTCTTTCTCCTCAATCCCCTCTACAGTTCTTCTTCCCACCCATCTCCCCTTATGTCATGCGGAAACGCAGGCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25418
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128704 | Nonsense | 697 | 800 | 9 | 9 |
ENSDART00000139138 | None | None | 161 | None | 4 |
ENSDART00000147378 | None | None | 136 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 9901224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9701775 |
GRCz11 | 9 | 9679812 |
KASP Assay ID:
554-7333.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGAGGAGTAAAAGGGCAGAGAAAGCACAGACTCAGAGCAACTCAGGA[C/T]AGGACAGTTGGCAATGTTCTTCTCACAAATGTTCGATTACTCCTTTCATG
Long Flanking Sequence:
CTTCTACTCAGTTTAATTTACCTCAGGTTGAGTCTCCAGTGCCTTCAGCCTCTGTTGAGCTCCCTGCCATTTCCCCAGCAGGTAGACTGGGCTTTGTGACCAATGAGCAGCTGGTGGAGATCTTGCAGGATCTGAGTATAGATGCTGTAAGCAGCTCTGTCAAATCACCCGACAGGGCGAGGAGCCCATCTATCAATCCAGATGAACTAAGCATGACTCTTTCTCCTCAATCCCCTCTACAGTTCTTCTTCCCACCCATCTCCCCTTATGTCATGCGGAAACGCAGGCCTCCATTTTACTCTTCAAAAGGTGGACCTCCACCTTACTACTTTCCAGGCTCGGTTCCTCCAGGTCGAAGGAGGGGACTTCCAGACCTTGAAAAGTTCAGGGATGATGACCCTATAACAAGTTCCACTGGTAACCCTCAAAGACATGACTTGTTGCGTGAGGAAAGGAGGAGTAAAAGGGCAGAGAAAGCACAGACTCAGAGCAACTCAGGA[C/T]AGGACAGTTGGCAATGTTCTTCTCACAAATGTTCGATTACTCCTTTCATGGGACATGTTCCTCAGCCAGCCTCCGCTGGACTGATAGAGGAGGTTAAACACTCTAAGGAGCCATATGACTATTCAGACTCAGACTCCAGCAGCTCGGAGGACTACTGTTACTACCAGCGGTCCTACTGTAGAGCATGTCATCACCCCTATGACTCTACAGACAGTCTCACCTCAGGGACATCAGACAGTGAGGACGAGGATTTCTACCGCTTATCACATCCTGTCGTGAACTTTAAAGTCGATGTTAAACCAACCTTTGTGTGATCTACAAATCCATTGTTTGTTTTTTGAAGTGATGTGATATTTTATTTTGTTTGGCTGGACCTTATTAAGTTATTGATATATACATGCGATAGTTAAAAGATTGATTTTTAAATGTTTTTCAAAGAAGCTATGCTAATCAAGGCTGTGTTTATTTGATCATGCAGTTAAAATACTGTAGTGGTAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34566
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128704 | Nonsense | 737 | 800 | 9 | 9 |
ENSDART00000139138 | None | None | 161 | None | 4 |
ENSDART00000147378 | None | None | 136 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 9901102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 9701653 |
GRCz11 | 9 | 9679690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCTGGACTGATAGAGGAGGTTAAACACTCTAAGGAGCCATATGACTA[T/A]TCAGACTCAGACTCCAGCAGCTCGGAGGACTACTGTTACTACCAGCGGTC
Long Flanking Sequence:
TTGCAGGATCTGAGTATAGATGCTGTAAGCAGCTCTGTCAAATCACCCGACAGGGCGAGGAGCCCATCTATCAATCCAGATGAACTAAGCATGACTCTTTCTCCTCAATCCCCTCTACAGTTCTTCTTCCCACCCATCTCCCCTTATGTCATGCGGAAACGCAGGCCTCCATTTTACTCTTCAAAAGGTGGACCTCCACCTTACTACTTTCCAGGCTCGGTTCCTCCAGGTCGAAGGAGGGGACTTCCAGACCTTGAAAAGTTCAGGGATGATGACCCTATAACAAGTTCCACTGGTAACCCTCAAAGACATGACTTGTTGCGTGAGGAAAGGAGGAGTAAAAGGGCAGAGAAAGCACAGACTCAGAGCAACTCAGGACAGGACAGTTGGCAATGTTCTTCTCACAAATGTTCGATTACTCCTTTCATGGGACATGTTCCTCAGCCAGCCTCCGCTGGACTGATAGAGGAGGTTAAACACTCTAAGGAGCCATATGACTA[T/A]TCAGACTCAGACTCCAGCAGCTCGGAGGACTACTGTTACTACCAGCGGTCCTACTGTAGAGCATGTCATCACCCCTATGACTCTACAGACAGTCTCACCTCAGGGACATCAGACAGTGAGGACGAGGATTTCTACCGCTTATCACATCCTGTCGTGAACTTTAAAGTCGATGTTAAACCAACCTTTGTGTGATCTACAAATCCATTGTTTGTTTTTTGAAGTGATGTGATATTTTATTTTGTTTGGCTGGACCTTATTAAGTTATTGATATATACATGCGATAGTTAAAAGATTGATTTTTAAATGTTTTTCAAAGAAGCTATGCTAATCAAGGCTGTGTTTATTTGATCATGCAGTTAAAATACTGTAGTGGTAAGGTCTACTTAATATTTAGCTTTACAACCACATGAATTAGTTACATTTTTACTGAAATAAAATAGAAAACAGATTTTTTGAAGTTCTTTAAGGTAAAAAAAAATGGTTCACAATAAAATTCCATA
Associated Phenotype:
Not determined