ZMP
tas1r2.2
Ensembl ID:
ZFIN ID:
Description:
taste receptor, type 1, member 2.2 [Source:RefSeq peptide;Acc:NP_001077325]
Human Orthologue:
TAS1R2
Human Description:
taste receptor, type 1, member 2 [Source:HGNC Symbol;Acc:14905]
Mouse Orthologue:
Tas1r2
Mouse Description:
taste receptor, type 1, member 2 Gene [Source:MGI Symbol;Acc:MGI:1933546]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21380 | Nonsense | Available for shipment | Available now |
sa21379 | Nonsense | Available for shipment | Available now |
sa21378 | Essential Splice Site | Available for shipment | Available now |
sa34487 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21380
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 |
---|---|---|---|---|---|
ENSDART00000082509 | Nonsense | 261 | 823 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 48820044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46622905 |
GRCz11 | 8 | 46613136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGATTGATATGCTTAACGTCAATGTCATCGTTGTTTTTGCTGAACAG[C/T]AGTATGCCAGCAACATTATCAAAGCAGCGATAGCAAACGACGTTCGTGAC
Long Flanking Sequence:
AAACTGTTAATTTACAGATATTTTTAACAATGTGTACTGACAACTACCTTGCTAATTGTGATATTTCTGAAGGAAACTGTCAGTTATTGAAGAATATCTGTTTGCTAATCTTAAGTGTTACCTTTTTGTCTTTATTTTAAGAAATACTGCAATAAATAGCATCATTTTCTTCTTCTCCAAAGGTGAATTATGGAGCTTCCAGCTATTCGTTGAGTAATAAACTCATGTACCCGTCTTTTGTAAGAACGGTGCCCAGCAACAAAGACCTGATACATATGATTATTCAGATCATACAGTGGTTTGGATGGAACTGGGTCGCCTTTCTTGGTGACCAAGATGATTATAGTGAAGATGGCTTAAGGCTGTTTAACACGTTTATAAGCAACTCTGGCATTTGTCTGGCCTATCAAGAGGCTTTGAGCCAAAAGACAAACTACAGTCTAACGTTTGAAATGATTGATATGCTTAACGTCAATGTCATCGTTGTTTTTGCTGAACAG[C/T]AGTATGCCAGCAACATTATCAAAGCAGCGATAGCAAACGACGTTCGTGACAAAGTATGGATTGCGAGTGAAACATGGTCAATGAATCAGCAGCTACCAAGGGAGCCAGGGATTGAGAAAATCGGTACAGTCATTGGCATTACAGAGCGATTCTTGTCGTTACCTGGATTCAATGAATTCATCTATAAAGAAAGGCGATCAGTTGATGATGCTGGTCATAATCATGGTATGGGTGAAGTCAAAAGCCAGACATGTAATCAAGACTGCGATTGCTGCACATTGTTGACTGCAGAGGAGATTATAACTGAAAATCCAACATTCACTTTCGGTATCTATTCGGCCATATATACCATAGCTCACGCACTGCATAAAGTCCTGCAGTGTGACGTGAATGTTTGTGACAAAAACACAACAGCTAAGCCTTACATGGTGAGTGAATTAATCATAAGATTTCATTATCATCATAATGTTACTTCAACCTGGGCTCATTTTGAAAACGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21379
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 |
---|---|---|---|---|---|
ENSDART00000082509 | Nonsense | 310 | 823 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 48819897)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46623052 |
GRCz11 | 8 | 46613283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGGGAGCCAGGGATTGAGAAAATCGGTACAGTCATTGGCATTACAGAG[C/T]GATTCTTGTCGTTACCTGGATTCAATGAATTCATCTATAAAGAAAGGCGA
Long Flanking Sequence:
TGCAATAAATAGCATCATTTTCTTCTTCTCCAAAGGTGAATTATGGAGCTTCCAGCTATTCGTTGAGTAATAAACTCATGTACCCGTCTTTTGTAAGAACGGTGCCCAGCAACAAAGACCTGATACATATGATTATTCAGATCATACAGTGGTTTGGATGGAACTGGGTCGCCTTTCTTGGTGACCAAGATGATTATAGTGAAGATGGCTTAAGGCTGTTTAACACGTTTATAAGCAACTCTGGCATTTGTCTGGCCTATCAAGAGGCTTTGAGCCAAAAGACAAACTACAGTCTAACGTTTGAAATGATTGATATGCTTAACGTCAATGTCATCGTTGTTTTTGCTGAACAGCAGTATGCCAGCAACATTATCAAAGCAGCGATAGCAAACGACGTTCGTGACAAAGTATGGATTGCGAGTGAAACATGGTCAATGAATCAGCAGCTACCAAGGGAGCCAGGGATTGAGAAAATCGGTACAGTCATTGGCATTACAGAG[C/T]GATTCTTGTCGTTACCTGGATTCAATGAATTCATCTATAAAGAAAGGCGATCAGTTGATGATGCTGGTCATAATCATGGTATGGGTGAAGTCAAAAGCCAGACATGTAATCAAGACTGCGATTGCTGCACATTGTTGACTGCAGAGGAGATTATAACTGAAAATCCAACATTCACTTTCGGTATCTATTCGGCCATATATACCATAGCTCACGCACTGCATAAAGTCCTGCAGTGTGACGTGAATGTTTGTGACAAAAACACAACAGCTAAGCCTTACATGGTGAGTGAATTAATCATAAGATTTCATTATCATCATAATGTTACTTCAACCTGGGCTCATTTTGAAAACGTACCACTATATACATTTCTGGAGAGCGCCAAATATGTCCCAGAAGCTACGTTTTTTTTTGTTTTTTTTTGCAGTTTTAGTTTTTCGCGAATTTACAAGAGGCTGGTGGATACGATTTCAAATTTCTCTCGCTAGTGCCAGTCGCACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21378
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082509 | Essential Splice Site | 473 | 823 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 48818553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46624396 |
GRCz11 | 8 | 46614627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTATCCGACTTGTTTTGATGTTAACCTCATATTTTTTCATTCCACAA[A/C]GGTTCCTTTCTCAAACTGTTCTGCTGAGTGCAAGGAAGGATTTGCAAGGG
Long Flanking Sequence:
ACTGGACAAACTGGTAGCAGCGGGAAAGCTGTCCATACGGAGGTTAGCGGTCAGCTGATAGCACGAATAGGAACAGCATCATACCGCCTGTTGTGTTCATTTTAAAGACGAAATGCAGCCATATGTACTTCAGGCTACATATTCATGATCTCCAGAAATGTATATGCTTTCAGATTTGAGCCTATGTTGCTCTAATTTGTATTTTTTTTTGGCCATTTTAGCTTCTTGAACAAATAAAGAAGCTGGATTTCCCACTCAATGGCCGTCAGGTGAAATATGACGCAAACGGTGATCCAACTATCAGCTTTGCGATCATACTCTGGCATACTGAAACAGATCCTCCACATTTTGATAAAGTGGGCATGTTTGATACATATCCTGAAGTAACTTTTACCATCAACAACACTCTCTTGCCCTGGCATAACAATGTAAGTTTTCTTTTGGGAAAAACAGTTATCCGACTTGTTTTGATGTTAACCTCATATTTTTTCATTCCACAA[A/C]GGTTCCTTTCTCAAACTGTTCTGCTGAGTGCAAGGAAGGATTTGCAAGGGAACACGATAGATTTCATACTTGCTGTTTTCTGTGCAAAAAATGTCCACGGAACAGCTATGTGGATTATACTCGTGAGTACTTCAAGCGATAAAATTGTGTAACATGTTAGCTTCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATATATATACACACACACACACACTCACAAGCCACTTTATTAGATACACCTGTCCAACTGCTTGTTAGCGCAAATTTTTATTCAGCCAATCACATGGCAGCAACTCAATGCATTTAAGCATGTAGACATGGTCAAGACGATCTGCTGCAGTTCAAACTGAGCATCAGAATGAGGAAGAAAGATAATTTAAGTGACTTTAAATGTGGCATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34487
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 |
---|---|---|---|---|---|
ENSDART00000082509 | Nonsense | 800 | 823 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 48813634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 46629315 |
GRCz11 | 8 | 46619546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAATTCTCTTCAGCTACTTCATACCAAAGTCTTACATAATAATATTC[C/T]AACCACATAAGAACACTCCGGCATACTTTCAGACATCTATTCAGAGTTAC
Long Flanking Sequence:
TGCGCTCCTTTCAAATTGTTTGCATTTTCAAAATGGCTGCCAAGTTTCCTAGCATGCACAGCCTTTGGGTCAAGCACAATGGGCAGTGGCTCTTTGTCGGGTTTTTTTCAATCATTAATATAGTTTCTTGCATGCTGTATATGACTGTCTCACCTCCCAAGCCCTTCAGAGACTCGGTAACCTTTAAAGATCAGCTCATTCTCAGCTGTGAGATTGGGAACACTGTAACTATTAGCATGGTTATGTTTATAGCATGGTTTCTCGGTTTCCTTTGTCTCGTATTTTCGTACATGGGAAGAGATCTGCCTAAGAATTACAATGAGGCAAAATCGATAACCTTCAGTCTCATCCTGTACTACCTGAGCTGGATTGTGTACTTCACAACATACCTCATGCTTAAAAGCAAATACATTCAGCTTGTTAATGCGATGACAGAGTTATCCAGCATTTATGGAATTCTCTTCAGCTACTTCATACCAAAGTCTTACATAATAATATTC[C/T]AACCACATAAGAACACTCCGGCATACTTTCAGACATCTATTCAGAGTTACACCCAAACCATTAGTAGAACTTAAACCACAAAACAGCGTTTATTTCCTGTCCAAATTATACATGTGTTTGCTATACCTAGAGGTTGTGTTTGGATTTAGAAACAATGTTGTGAACACTCAGTCTGGGAGTAAGCTTAATAATGTCATTAAGTTAGATTCTTCACTGTCATGTTACCTTTAAAAAAGTGTCTAGGTTTCATTGTGCATTAAAATGTTGTTTGTTTTAAATAGATTTATGTTAAAGGGCGCCAATTTTACCCATTTCACAAGATGTAAAATAAGACTTCAGTGTCTCCAGAATGTGTCTGTAAAGTTTCAGCTCAAAATACCTGTCAGAATTTATTATATAATGTAGAATCTGCACATTTCGGTGTCTGATCACAATGTAGCTGTTAATATAGGCTTTAAATGCAAATGAGTGGTTTCACCCCGCCCACTGCTCTGACGTGC
Associated Phenotype:
Not determined