ZMP
si:dkey-259j3.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
GPR64
Human Description:
G protein-coupled receptor 64 [Source:HGNC Symbol;Acc:4516]
Mouse Orthologue:
Gpr64
Mouse Description:
G protein-coupled receptor 64 Gene [Source:MGI Symbol;Acc:MGI:2446854]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11602 | Essential Splice Site | Available for shipment | Available now |
sa18436 | Nonsense | Available for shipment | Available now |
sa41703 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa4382 | Essential Splice Site | F2 line generated | Not yet available |
sa15869 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11602
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123936 | Essential Splice Site | 17 | 1356 | 1 | 36 |
ENSDART00000131350 | None | None | 720 | None | 14 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 36353388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35386090 |
GRCz11 | 10 | 35329950 |
KASP Assay ID:
2260-3497.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTTTYCTACAGATCATGTTAAAAATCACAGCATGAAACTGTCCACAAG[G/A]TATGTCATTTTRTGTTTATATGATTGWCTATATGTAAATGTGATGGTGAT
Long Flanking Sequence:
CTCTAATTTTTTGAATAATAACAAATAACTCTAAATGACAATATTTAATTCGAAATGAGAAGTGTCCTTTTTTTTAAGAATAAAACAAATTTTAACATTTTACTCTAACTTATGCATCACATAGTAAATCAAAAGAAATGATAATACACAAGATCTAATGTATGCATATGCCCTGTAAATATAGTTTTAACTTCACACTACAGGTAGTATTCCTGTGTGCCGAAGGGGAAGCGCCGGTGTTTTGTAGGTTGGGTGTGTGTGTGTTGAAGTTTTAGGTTAACGTGGGTGGTGCACATAACTCACTTCTCACTGAAACACATCACAGGACAGACAAACCTGAGCGGATTTATAAGCAACTTTAGTCTAAGTTTTTTTCTTAGGAAATTTTTGTCAGATCTTCATTTGGGAAAGCAGCCTGTGGTTGCTGTGTGTTGTGTGTCAGGAACATCCATGTTTTCTACAGATCATGTTAAAAATCACAGCATGAAACTGTCCACAAG[G/A]TATGTCATTTTATGTTTATATGATTGACTATATGTAAATGTGATGGTGATCTGTTGGTTTTGTAATGTTTAATGAACTTGTGTGTGTGTGTTTTTAAGGTTATTTGTTGTTAATAAACAATAGAAAATATCTGTAAAAATTTACTGTAAAATAATACGGTAAACATATAGTAGATAGCCTACATTAAAATCATTGCTTTATTTTGAGTGACATTTTTATTTAACAATATCAAAATTAACCTACAACGTGCTTTCTGATATATAATCAGAGGCAGGTTTTACAAAGAATGTGCAATGGCTTATAGTCCAAATGTACTACAAAATCACATCATAAACAATAGCAGCAAATAGGTCAACTAAGTATTTACCAAATAAACAAATACAATAATTTTTAAGGGCAAAACAATAATAAAGAAATCATAGTAATGCTTAAAAAAGGGTCACACTTTACAATGAGGCTTCATTAGTTAATGCATTTACTAACAAAAACTGATTATGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18436
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 |
---|---|---|---|---|---|
ENSDART00000123936 | Nonsense | 425 | 1356 | 13 | 36 |
ENSDART00000131350 | None | None | 720 | None | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 36366355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35399057 |
GRCz11 | 10 | 35342917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTGTGATGATGATGAACTCGGCYGACATCGAAATCAGTGTGGAGGGA[C/T]AAATAGAAAGAGTGGGTTAGTGAAATACTACTAAAATTGTCTTTCGGTTG
Long Flanking Sequence:
CAATACGTAATTTGTTTGCTCTCTTCAACTGTATGCATCAATGACTTTCAGTGGCAGATGTTAAATGCGTTAACTTTTTTTTTTTTTTTACCTTGCATTCTATCTGTTCAGCAGTCCAGTAACAACATATCCTGGCCTGTTTGAAGTAAGTGCAGAATCAGTTATTTGCATTTGCATTACTTAGTATTTCATCATAAATCATATAATAAACATCAACTAAATGTGCTTTTATTTTTCCTCATCAGGCCTTGGAGATCACATGTGATTCAAACATTATGAAGTCAGTATCGACTGCTACTCTTATCCAGCTCAAACATACATAAGCAATAGATGAAATTGGTGTACTGCTAAAAGGTTTGCTCAAATAGTGTTTTTTTTTTTTTTTAAGTAATTCACAATGCTACGTTCTTCTGAAGCTGGCAGCACCTGCCAATGTTTGCTGCATTAGAGACACTGTGATGATGATGAACTCGGCTGACATCGAAATCAGTGTGGAGGGA[C/T]AAATAGAAAGAGTGGGTTAGTGAAATACTACTAAAATTGTCTTTCGGTTGTCATAATAATAATAATAATAATTTATAATGATAATTAATTAATGAGTTTTATGAATAAATCATTAACAAAGTTGTAATGAATGTTAGAAAAATAAATATATTTAGGCTACTTTGTACATTAATGGTAATACATTGTACTAGTTTAATATCACTCTTGCTAGAATATGTGACAATATGTGATCTGTTGTTGGTGTTTCAGGTGTGTGTGCAGATGATTTAACTCAGATCTTCGCTGGACAATATGATAAATGTGATCAGACTCTCAATATTGATGTATGCAGCACACAACCACAGAACATCTCATGGTAGGTTTAGACTAAAAACATGAAGTATCATGTTTAAAATAAAGTACAGAGTACATCACTTTAATATGTTTAAATAAAACTATCATTGTGTGAATTTCTTGTTTTTCTATCATAGTGGAAACAGTACAAATGTGATTTTCCCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41703
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 |
---|---|---|---|---|---|
ENSDART00000123936 | Nonsense | 461 | 1356 | 14 | 36 |
ENSDART00000131350 | None | None | 720 | None | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 36366697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35399399 |
GRCz11 | 10 | 35343259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGATAAATGTGATCAGACTCTCAATATTGATGTATGCAGCACACAACCA[C/T]AGAACATCTCATGGTAGGTTTAGACTAAAAACATGAAGTATCATGTTTAA
Long Flanking Sequence:
TACTGCTAAAAGGTTTGCTCAAATAGTGTTTTTTTTTTTTTTTAAGTAATTCACAATGCTACGTTCTTCTGAAGCTGGCAGCACCTGCCAATGTTTGCTGCATTAGAGACACTGTGATGATGATGAACTCGGCTGACATCGAAATCAGTGTGGAGGGACAAATAGAAAGAGTGGGTTAGTGAAATACTACTAAAATTGTCTTTCGGTTGTCATAATAATAATAATAATAATTTATAATGATAATTAATTAATGAGTTTTATGAATAAATCATTAACAAAGTTGTAATGAATGTTAGAAAAATAAATATATTTAGGCTACTTTGTACATTAATGGTAATACATTGTACTAGTTTAATATCACTCTTGCTAGAATATGTGACAATATGTGATCTGTTGTTGGTGTTTCAGGTGTGTGTGCAGATGATTTAACTCAGATCTTCGCTGGACAATATGATAAATGTGATCAGACTCTCAATATTGATGTATGCAGCACACAACCA[C/T]AGAACATCTCATGGTAGGTTTAGACTAAAAACATGAAGTATCATGTTTAAAATAAAGTACAGAGTACATCACTTTAATATGTTTAAATAAAACTATCATTGTGTGAATTTCTTGTTTTTCTATCATAGTGGAAACAGTACAAATGTGATTTTCCCAGTTGGTGTTAAGGAGAACTGCACTGTTATTCCAGGTAAGGCTTCTTTTAGCATTAGCTGTGCTTGTCACGTTTGTCATTCATCATACTTGGAGATAAAGCTTTAGACACAACTTCAACAAATTCCCTTTGATTGTGAATAGGGACACATTTTGACAAATCTCAGAGTAAAGGACTTTATAAAACAAGTGAATTAACACATTTAAAGAAGCAGACACTTTTGCAACCATCTAGCAACACTACACCAGCAATCAACTAGGAAACACCCTAACAACCACCTATAACACCCTATCGTGTTTCCTGCCTGCCCAGCAAGCACAGGTCATCAACATGACGTCAGATTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4382
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123936 | Essential Splice Site | 535 | 1356 | 18 | 36 |
ENSDART00000131350 | None | None | 720 | None | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 36368959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35401661 |
GRCz11 | 10 | 35345521 |
KASP Assay ID:
554-3523.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCTACAGGTTTCTCAATTGTTCAGTAATTCAACRTGCAGCGGCGCGTC[G/A]TAAGTTGTACCCTTTTTGTTGTGTTAGTTCACTGAAAGCAATCTAAACAT
Long Flanking Sequence:
AACTCACTTTTTCTTAAAAAATGTACATCCGATTAAAAAAAAGGCTCATGAGAAATGTAGCAAACATTAAAGACCTTTAATTTATGCTCTTGAAAAACTATATGTTTATGACGGGTGTGCCGTTTATTATGTCTTCTGTTGTTTTCCCTTAAAGCAACACCAGGGTGTAACTGTTCTTCACACTGCAGTAATTCAGGTAAGACAAGCGCATCGTGGATGGAATCTGCTGTTAAAGCACAAAATAATATCTTTAAATGCGTTTGATTTTTGCATTATATTTACTCTTCTTCCTCTCTTTTAGATTTCTACTATTACAGTTTTAGCCTTGGTCATTCAACTTCTTCAGAAAACACTGGATGCCAATCTGTAAGTGTCATGTCTCACTGCAGACAGATCATTCAGTGCTTTTTTAAAGGTACAGGATAGAGATAAAGAATTGCATTGTGCTTTTTTCTACAGGTTTCTCAATTGTTCAGTAATTCAACGTGCAGCGGCGCGTC[G/A]TAAGTTGTACCCTTTTTGTTGTGTTAGTTCACTGAAAGCAATCTAAACATGCATTTTCCCATTGTGTGCATTTTACAATGATTTTATTTCTATACATTCTGTATATTCTTTCTTATAAAAATATTGTCATTGTAAAAGTATTTTTTTTCCTCTTGACAACATCAACATTCCATAATGTAATTCAAAAGCATAAATCATGAGCTACTGTTGATTAAAAGATACGTCTGCGTTTTTTAAAACTCATCTCTTTTAATTTTGCGTTGTAGATCTGCTTGTTATAGTCTGACAACTTTACGCAATCATTTTCAGGTAAGATATCATGACAGTAAAAGATTTTTTCTCAGTTGGGGTTGATTTCTCTTAACTGTTTCTTAACTGTTTCTGCAGGACTTGAGAGCGGAGAATTCATCTGGACGGTACGTTGAGTTTCAGAGCAGAATTGAAGTCTGCTCTACAGCTGATGGGTTGTTAATATACTGCTTTTTCCATTTCAGTTTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15869
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123936 | Essential Splice Site | 1019 | 1356 | 30 | 36 |
ENSDART00000131350 | Essential Splice Site | 418 | 720 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 10 (position 36378307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35411009 |
GRCz11 | 10 | 35354869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRTCGGCWATTTTCCTGTCTGTCACCCTGCTCACTTATCTGGCCTTTGGG[T/A]AAGAAAAATGCTTTGCAGGTTCAACATTCAATGCCTGAATTTTAGTATAT
Long Flanking Sequence:
TCAAATATATCCCAAATGCTTTTTGATGGAGAGAAGATTTTTTTCAACACATCTTTAACATAATAGTTTTTATATCTATTTTATAACAACTCATTTTTTGTCTCTGGCATATTCTAGTATAGTTGGCTTAACTAGGTTAATTAGAGTGAACTAGGAAAGCTAATTATATACTGTATACATACAGTATATAGAAAGCCAAGCATAATCAGTGGATAATCTGCCGCATAATCATAATTTGCTTTAAATAGAATAAAAGTGGTTGCTATCTTTTATTTTTGCTAGTTTTTGGAGTTTTTTGCAGAGAAGCTGGTGTAATTTTTTTGTCAGTGGGCCTGACATGTTTAATTCTTATAGTTATGTTTAATCTTGGTTGACAGGACATTTCAAAGACTGAAATCCCTCCTTTGGATCTCCTTATTCTGACATACATTACATACATCGGCTGTGGCATATCGGCTATTTTCCTGTCTGTCACCCTGCTCACTTATCTGGCCTTTGGG[T/A]AAGAAAAATGCTTTGCAGGTTCAACATTCAATGCCTGAATTTTAGTATATTGTATGATATATTATGTATTATTGTATCATATATGTATGATGTATATTTAAATATACATACAAACATAAGTGTACATTTAATTACATTTTACAGTATTAGCAAACCTACATTTTCAGTTTCAAACTTTATCATCATTAACATCCTGATATCTGAAGCTCAAGAAACATTGCTTATGATGATAAATGTTAAAAGGTTGTTGTGTCACTTTGATTAATTTAATAATACATTTTTTATAATCATTTAAAAGTCTGTTTTCTATTAGATCAATGCATCCTTGCTGAAATGAAGTGATGAAATGACATTTGAATGGTAGTGTATGTATAAAAGACAATATACATTTTTTTAATCTATGCAGCAAACTGCGCAAAGACATCCCATCCAAGATCCTGATTCATCTGTGTTTCGCCTTGCTGCTGTTAAACCTGGTGTTCCTGCTGGATGCCTGGTTG
Associated Phenotype:
Not determined