ZMP
wu:fc49b10
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC324948 [Source:RefSeq peptide;Acc:NP_001018317]
Human Orthologues:
GPR114, GPR56
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 56 [Source:HGNC Symbol;Acc:4512]
Mouse Orthologues:
Gpr114, Gpr56
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 56 Gene [Source:MGI Symbol;Acc:MGI:1340051]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11235 | Nonsense | Available for shipment | Available now |
sa20956 | Nonsense | Available for shipment | Available now |
sa20955 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11235
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033921 | Nonsense | 44 | 648 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30016561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28409084 |
GRCz11 | 7 | 28680277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACAGAGACTTCAAKATGTGTGGAAAGTGGCTCCATGGCATCGCACCT[C/T]RAAATCTGGAATATGATTTRAAAACYGGCTGTGAAAGWATTGAMATTTYA
Long Flanking Sequence:
ATTTGTGCCCACATAACTGCCGCTCACTGGATATTTTCTTTTTATCTGACCATTCTCTGTAAACCCTACAGATGGTTGAACGTGAAAATCCCGGTAGATCATCAGTTTCTGAAATACTCAGACCAGCCCGTCCGGCACCAACTATCATGCCACTATCATGTCACTTAAATCACCTTTCTACCCCATTCTTATGCTCGGTTTAAACTGCTGCAGATCGTCTTGATCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCATGTGATTGGCTGATTAGAAATTTGTATTCATTAGCAGGTGTACCTAATAAAGTGGCCAGTGACTATGTATATAAAAAGTATTATCATTGTTTTTTTTATTATTATTATTATTTGCAGCTAACACATTTATTTATTTACAGCATATTAATACATTTTTTAACACAATTTGTTTATCTAACAGCAACAGATAATGACAGAGACTTCAAGATGTGTGGAAAGTGGCTCCATGGCATCGCACCT[C/T]AAAATCTGGAATATGATTTGAAAACCGGCTGTGAAAGAATTGAAATTTCAGCCAATGAGAGCACGCTCTCCATTCAGGGCAGGATCACAGCCAAGTGCACACAATCTTCATCCATTCAACTAGATTCAAATCCTCATCAGAATCAAAGTCATTTCTGTGTGTTCTGGGAGCCGCTGCTGGACCTGCTGATAGTGGAGGTCAATGGCAAGAATCACACTCTATGTAAACCAAACGGCCTTCAAGGAACCTGCTGCACCGACCTCTCACAAGGAGTTCAAGACAATGCTCATATGTATGGTATTGTGAATGGCAGTGTCAAAGGTGATATCATCACAGGTGATCTCAAGGGAAACTACATATTTGATGGGGCTCATATCAACTGCAGTAAGAATCTTTATTTTAATATGTCATAATTTGTTTTCTCGTGAATTAGAGATATCAGATGTATTCATTTAATCTCTTTTTTGATTAATAGAGGAGAAGTTCTGTGATGAGGCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20956
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033921 | Nonsense | 229 | 648 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30015172)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28407695 |
GRCz11 | 7 | 28678888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTCTAGCATATGCAATAATATACTTATGTGTTGCATTTCAGGCCCCT[C/T]GATTTGTAGACGCAAACACCATACCCTCCGTTTATATTCCATCAAGCCTG
Long Flanking Sequence:
CTGCATGCTTATTTTGATGCATACAGTATATGGGTGGGTCCACTGTGGTTTACTTTATAACCATAACACATACAAGCCTTCCGCCCCAAATACCATAAATAACTCTTTTTGTGGTATTGTGGGATATAGGCGATTTGGGCGTACATGAATGCAGCAATCTATGAATCATACATTGAATAAATTTGGTATTTAACTTGATGTGGATATGTAATAATGACTTACAATACTTTAAACACGTGAGGTTTGTTGTAGTGTGTTCACATTATAATGCATGTGTTGGTGTTTGTTTGCAGGATAGAGGAAGTAGTGATGAGATTCAATGCAAAGGGTCGTGTGGATCTACCTTGTGCTCAGGGCACAGTCATTGAGATGGACGAGGAATTCACAGGACACAATTTCACCGTGCCTGTAAATGACTTTGACCTTATTAGAAGCATTTGCAGGAAGGTCTCTTTCTAGCATATGCAATAATATACTTATGTGTTGCATTTCAGGCCCCT[C/T]GATTTGTAGACGCAAACACCATACCCTCCGTTTATATTCCATCAAGCCTGAGATCTGTATCAAGGAGAAAATCCAAAGTGGTGTGTACTTACTACAAGAACAAGACGTTATTTGAGGTATGATGGTGACATTTGATGAATATAAAGAAATCATGTGGATTTTTTATCTTCCTTACCAACATATTTTCAGTATGATATATCAGTATTTGTGTTTGTGTAGCGAGGACCGTCTAAATCAGCTCTTCTGGATGACATTGTGGGACTCTCTGTGGAAAATGAGACTATCAGAAACCTCATAGAGCCTGTCAAAATCCGGTTCCATCACCGTCCCTTTGCTGTAAGTGGAAAAAGCACATTGGGGTGCTGTTCTAGTACTTTTTAACATTATACTGCATGGTGTGAGATACAGCAACTGTAGCTCACACCAGTTTCTACTGTGTAGACTAAATGTCTTCCATTTCCTTAACACTGAAACCACATGACCACATGCTAAGGTGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20955
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 |
---|---|---|---|---|---|
ENSDART00000033921 | Nonsense | 593 | 648 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30007840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28400363 |
GRCz11 | 7 | 28671556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTATGGAACCACATGGGCTCTGGGTTTCCTCGATTTTGGCCCTTTCT[C/A]AGAGGTCACCCTCTTTCTTTTCTGCATTATCAATTCCTTACAGGGTGAGT
Long Flanking Sequence:
TGGAGAGACAATTTTTTTCTGAGGTGGTACTTGATGAAAAAAATTTGAAAACCACTGGTCTAGACTGTTTTGTCTTCCATTAAATAATTGGAAAAACTGGACAAGGATGAAACTTATAAGTGTCTGTGATTGTTCTCTTGTACTGAGTATACTTTGAAAGACTGCGTGAACACTAATGCAGATCTAACTAAAGTATTGCCTGGGCTTTATATATAATAATCATGCATGCAGTACATAGAAACTAATATATACTTTGCTTTGCTCATTTAGGTGCTGGATGACAGAGGGTGATAAGAGTCAGTTGGCTCATTACATCATCAACATTGGCTTACTGGCAGTTGTGGTGAGCTCTGGTTTAGTCATGCTTTTCCTTGTGGTGAGAGAGATCCGGAACAGACCAGACTGGAAAAAGATCCATGTGGCTTTTCTCAGTATCTGGGGTCTCACCTGTCTGTATGGAACCACATGGGCTCTGGGTTTCCTCGATTTTGGCCCTTTCT[C/A]AGAGGTCACCCTCTTTCTTTTCTGCATTATCAATTCCTTACAGGGTGAGTTTTTTTTTTTCTTGCACTATCACAAAATACACAAAGTCAAAAAATGCCTTTGCTATTGTGTCAAATGTAAGCTGAGTTCCTGTGGTGGGATTTAAAAATAAATCAAGCCTGAAACGTGTTTCCTTTTGTTATCTTTGAATGTTTGCTTCAGAAATGTAACTCAATAGCTTCCATTCTCTTATATTAAATGATTAATTACGGTAATATTACATTTCTATGTGTCTCAACAGGATTTTTCCTCATGCTGCGATACTACGCTCTTGAACGGATGAAAAAGAAAGATGTTTCAAGTTCGGATGGGAGCAGTTCTGGGTCTTCAAAACAGCATATGCTACAAACTAACGAGAAGAGTTAAAAAGTCTGGTGATGCTAAAACAGAAGCTGTCTGAAACTGCCAAATTACAGTTTTTATGATCGTGAAAGTTTATCCACAAAGGGCATTTGTAAAGA
Associated Phenotype:
Not determined