ZMP
gpr133
Ensembl ID:
ZFIN ID:
Description:
G protein-coupled receptor 133Novel protein similar to H.sapiens GPR133, G protein-coupled receptor
Human Orthologue:
GPR133
Human Description:
G protein-coupled receptor 133 [Source:HGNC Symbol;Acc:19893]
Mouse Orthologue:
Gpr133
Mouse Description:
G protein-coupled receptor 133 Gene [Source:MGI Symbol;Acc:MGI:3041203]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41283 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34472 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31670 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41283
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075372 | None | None | 240 | None | 8 |
ENSDART00000110688 | Nonsense | 128 | 485 | 5 | 12 |
ENSDART00000134073 | None | None | 240 | None | 9 |
ENSDART00000146152 | Nonsense | 27 | 186 | 1 | 3 |
ENSDART00000148358 | None | None | 359 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 46213199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43930290 |
GRCz11 | 8 | 43923709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTATCTGAACGGCGATAACGGGGCCACTTTCCTTCACTTTGGCAACTA[T/G]AAGGACTCCTGCATTAGTGATCCTACTCTCTGCGGACCTGCTGGTGAGTT
Long Flanking Sequence:
GGATGAGGGTCGGTCAGTCAATCGGTCGGTCAGCCAGCAGTGGCCTCTGGTGGATTTACGTGAGAACAGCAAGTGCGAATTGCACTTGCAAGAGAAATTTGAGGTCTTAAAAAGCGTACACAACGGCCTCTGGGGGATTAGCGAAAACAAAAACTGCAAAAAACTTAGCTCATGGTACGTATTTGGCGCTCTCCAGAAATGTTTATATCAGTATGTTTTCAGAATGAGCCTGGTTGTTAAAGTGACTCCAGGTGGCTCAATAATATAGCCTAAACTGGTATTTAAACTAAAGTGTTTCCAAAATCATCACTCAAAGGCTTTACATTTCAAAACAACAAAATTAGGCCCTTGCTGTACTGCACTGCTTTCTGAAATGAATTTCAAGTGTTATAATCTTGCTGGTTGCTTTCTCGTAATGTAGACATTGTAGAAGGAATGGTGAATAGAGGCATCTATCTGAACGGCGATAACGGGGCCACTTTCCTTCACTTTGGCAACTA[T/G]AAGGACTCCTGCATTAGTGATCCTACTCTCTGCGGACCTGCTGGTGAGTTTTTATTGTCCTCATTCACCCTTTTGCTGTTGATATAGAAGCACACTGAGATCTTTATATGGTCATAGATTTGTTGCTCAGGTTTATAGGTGACGTAATAAAGGCTAATGATTCAAAATTAAGTTTATATTTCTCAAGAGTAAATATATCAGCTTACATCAAGCGTTTCTGTGCGTGAAAGCTGAAATCATCTGTTATTCATCTGCTCACATCAGCGTTCGTTCCTTTGCTCCCAAAACTGAGAATATGTTGTGTTTATGTTTATTTTCCAGGGCTTGACCAAAGTAAGCCTTGCGATATTGTTTGTGATGGAAGCAGGCTGGATCTAATAAAGACGGTTTTGTTTAAAGATAGATATCTACATATCGGAAAAACTGTTTGGTGATAGCCAGAGGATTATGAAAATCTGATTAAATGTATTGATACATAACACTTTAAGTCATTTATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34472
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075372 | None | None | 240 | None | 8 |
ENSDART00000110688 | Nonsense | 164 | 485 | 6 | 12 |
ENSDART00000134073 | None | None | 240 | None | 9 |
ENSDART00000146152 | Nonsense | 63 | 186 | 2 | 3 |
ENSDART00000148358 | None | None | 359 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 46214152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43929337 |
GRCz11 | 8 | 43922756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCTTCTGGAAAAACAATGACGACGAGTCTCGTTTTGCGATCGCATCC[G/T]GAGGTAAAGTCATCTCAAGCGGTTTCTCAGTCTACTCAAATCCTTATGGC
Long Flanking Sequence:
AATCTGATTAAATGTATTGATACATAACACTTTAAGTCATTTATTATTGTTTTGAATTTACGATACAATTATATTTAACAAAATAAACTGCATGAAAAAAATTATAAGGAAACTTATTTTGGAAGGATTAATACATTTATTAGAGCATCAAAATGTAGCCTAAATACTGTAAGATTGTGTACTTATTTTATGAAGACTATGCTTCTTGATGTGAACATGTCGTTAGAATATAAAACATGTGAAAAACTCTTTAAGTGATGTGTGCCACATGTGAGTGTACAATACGTGGGACCAGAAGCACACACTTTAAGTCGCTATTCTTGTTTAAAACTAAATTCCCAAGTTTCAAATTCATGTTTCATAATAATTCAATGTTTCATAATTGTGTCAAAATATCTTAGATTCAAAGCTAAAGCTTTGCTTGTACTCTTACACCAGGGATAACGTTCTCCTTCTTCTGGAAAAACAATGACGACGAGTCTCGTTTTGCGATCGCATCC[G/T]GAGGTAAAGTCATCTCAAGCGGTTTCTCAGTCTACTCAAATCCTTATGGCGGATATGTGGAGTTCTACACCAGAGGAGACTTCAAGACATGGAAAGCAAATATCGAACTCCCAGGTACTTTGGGTGTCTGGGGAAATTTCAGTCTGAGTTGTGGAATGTGTGTTTTAAAGCTTCTGAGTATTTTGCTGAGTATCTCTGAGGAAAAGAAAAGATTTCCCATGGTCTTGAAATTTTGTACACATAGACTCATTCTGGTTTGGAATTACAGTTGAAATTCGACCATAAATATTTCAAACATATGTAGTTTTGCGCATAATTACATTGATTACATCCAGATGTCCACAAAGTATGCGAGTCGATAGGCTTCAGAATAAACTTTCTCTGTTGAGCTTGACAGAGTTGTTTACACTTGTATCTGACTGAAAAGAAAAGGAAGCGGGAGTGAAAAGGTGACAAATCATTCAGCTCCCTAGAAAATAATCAATACGGTTTTTCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31670
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075372 | Essential Splice Site | 178 | 240 | 6 | 8 |
ENSDART00000110688 | None | None | 485 | None | 12 |
ENSDART00000134073 | Essential Splice Site | 178 | 240 | 7 | 9 |
ENSDART00000146152 | None | None | 186 | None | 3 |
ENSDART00000148358 | Essential Splice Site | 297 | 359 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 46314126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43829363 |
GRCz11 | 8 | 43822782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAAGGGGTTCTTCATATTCCTGTTTCACTGTCTGTTAAACTCTGAGG[T/C]AAGTGTGTGTTTGTGCAGCTGTGACTGAAGTCTGTGCTGTGTATCTGGGG
Long Flanking Sequence:
AAAAAAAGCAATCTAGAAAGAAAAGTCACTAGACTTTTTTTCATGCTTATACATGTCTTTGCAGGCTGACGACCAAAGCAGTGGCTGTTCTTTTACCTATTCTGGGCATATCGTGGGTCTTTGGGGTTCTGGCGGTGAATGATCACTCTCTGCTTTTCCAGTACATGTTCGCAGTGTTCAACTCTCTTCAGGTCAGTTATCACTACTGTGTAACAAAACAGAGCTGCACAAATCACCACAGGTTTTACACAAACTGATCGATTTTCACATAGTTAGCGGCCTCCAAAGTCAATAGCATGTTGGCCAAACAATGACAGCTTTAAAAATACGAGACATAACGATGTTTGAAATGACTTTGGACCTGGACTGACTTGTAAGAACTGTTGCAGATGTGAATTGGAGCGCTTTCCACAACATTTAGCGTTATCTTTTGTTTTCTTTTTTTTTTTTCTCTAAGGGGTTCTTCATATTCCTGTTTCACTGTCTGTTAAACTCTGAGG[T/C]AAGTGTGTGTTTGTGCAGCTGTGACTGAAGTCTGTGCTGTGTATCTGGGGAAATGTCTGATGTAGCGAAGCAAACAGCATATGGCAAGCCGTGCTAACATTAACTCTAATAGCAAAACTATTGTATATATATTCATGCTAAAAACATTTTGGGATTTGATTTGTACAAAATAAAACAAACCAACCAAAAATTGTGAGAAAAAAATTATGAATTAAATAGCATAACAATTTAATTGTCTTCAAATAAACTTTACTAATTAAGCTTTACTAATTACTAATTGCTTTTCTAATAAGATCAACAGAATATTTACTTTTCAAGTACTAATAAACATCCAATATCTAAATAATAGGCAGGTAATAAGCCTTTAGTTATTAGTGAGAATTGATACTTAAAGAGCCCCTATCATGCTTCATAAAAGGTAATATTTTGTTTTTTAACAAAAATTAATTTGTTCCAAAACCCCTCCTTAGCATGAGGCTAATCTGCACTGATTGGTCCGA
Associated Phenotype:
Not determined