Busch Lab

ZMP

taar20z

Ensembl ID:
ENSDARG00000094065
ZFIN ID:
ZDB-GENE-060414-14
Human Orthologues:
TAAR5, TAAR6, TAAR8
Human Descriptions:
trace amine associated receptor 5 [Source:HGNC Symbol;Acc:30236]
trace amine associated receptor 6 [Source:HGNC Symbol;Acc:20978]
trace amine associated receptor 8 [Source:HGNC Symbol;Acc:14964]
Mouse Orthologues:
Taar5, Taar6, Taar7a, Taar7b, Taar7d, Taar7e, Taar7f, Taar8a, Taar8b, Taar8c, Taar9
Mouse Descriptions:
trace amine-associated receptor 5 Gene [Source:MGI Symbol;Acc:MGI:2685073]
trace amine-associated receptor 6 Gene [Source:MGI Symbol;Acc:MGI:2685074]
trace amine-associated receptor 7A Gene [Source:MGI Symbol;Acc:MGI:2685075]
trace amine-associated receptor 7B Gene [Source:MGI Symbol;Acc:MGI:3527438]
trace amine-associated receptor 7D Gene [Source:MGI Symbol;Acc:MGI:3527443]
trace amine-associated receptor 7E Gene [Source:MGI Symbol;Acc:MGI:3527445]
trace amine-associated receptor 7F Gene [Source:MGI Symbol;Acc:MGI:3527447]
trace amine-associated receptor 8A Gene [Source:MGI Symbol;Acc:MGI:2685076]
trace amine-associated receptor 8B Gene [Source:MGI Symbol;Acc:MGI:2685995]
trace amine-associated receptor 8C Gene [Source:MGI Symbol;Acc:MGI:3527452]
trace amine-associated receptor 9 Gene [Source:MGI Symbol;Acc:MGI:3527454]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa24884 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa21801 Nonsense Available for shipment Available now
sa34976 Nonsense Mutation detected in F1 DNA Not yet available
sa7340 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24884
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000142464 Nonsense 50 340 1 1
ENSDART00000144014 Splice Site None 295 None 2
Genomic Location (Zv9):
Chromosome 10 (position 41850488)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40563197
GRCz11 10 40484383
KASP Assay ID:
554-7486.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAGCGCAAGTCATGGATATATCATCATCTATGTGTTTGTGTCATTGT[T/A]GTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTC
Long Flanking Sequence:
TTCTTTGGTTATTTAATTTATATAGGTTTTAATTGAATTTTTGCTCAAAAGATAACCCTGTCTGACTCCACGCTTCTAGTTTGTCTCCTATTTTTACAGCACCTTTAATGAACATTAAACTGAAGGTCTGCTCAGGTTTTTTATTACATCACTGTGAACGAATGGCTATTTTAACAGTAGACACAGACCAGACATGTGTTATGGCTGCAAGATTTGACGGCATATCAAACTTAATGTGTATAAAAGATGGAAAAAAACAAAATGAATGCATTACATCAGAGTGGGCGGTAGGTGGGCTGGTCAGTCTGATCCAGACACTGTATAAATGAAAAGACAGAAAGGAGAACAGAACAAACTCCTAACAGGAGGAGACTCACTCATGGCCTACGAGACAGAGGATCAGGAGACTCAATACTGCTTTCCTGACATCAACTCATCATGTGTCAAGGGGAGAAGCGCAAGTCATGGATATATCATCATCTATGTGTTTGTGTCATTGT[T/A]GTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGTCTGTGGCTGATCTGCTTGTTGGATTCATCATGCCTGTAGAGGCCATCAGACTGACAGAGACATGTTGGTACTTTGGAGACACTTTCTGTTCACTCTATTTATTATATATTGCGGTACTTCTTTCTGCATCTCTTAGTAATTTTGTTTTAATTGCTCTTGATCGATATGTGGCTGTGTGTCACCCTTTACTGTACCCACAAAAAATAACCATCACTAAAACATTAATGAGTATCTGTCTGAGCTGGGCTTGCTTCTCAGCATATAACATTACCTTTGTTATTTATAATGGATATTTTGACACTTTATACAAAACAGATGTGTGTTATGGACAGTGTTCATTCATTATGAGCTTTCATTGGATAGTCACTGATCTGTTCATGTCTTTTATTTTTCCCTGTTTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21801
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000142464 Nonsense 194 340 1 1
ENSDART00000144014 Nonsense 166 295 2 2
Genomic Location (Zv9):
Chromosome 10 (position 41850055)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40562764
GRCz11 10 40483950
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGATATTTTGACACTTTATACAAAACAGATGTGTGTTATGGACAGTG[T/A]TCATTCATTATGAGCTTTCATTGGATAGTCACTGATCTGTTCATGTCTTT
Long Flanking Sequence:
TCATCATGTGTCAAGGGGAGAAGCGCAAGTCATGGATATATCATCATCTATGTGTTTGTGTCATTGTTGTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGTCTGTGGCTGATCTGCTTGTTGGATTCATCATGCCTGTAGAGGCCATCAGACTGACAGAGACATGTTGGTACTTTGGAGACACTTTCTGTTCACTCTATTTATTATATATTGCGGTACTTCTTTCTGCATCTCTTAGTAATTTTGTTTTAATTGCTCTTGATCGATATGTGGCTGTGTGTCACCCTTTACTGTACCCACAAAAAATAACCATCACTAAAACATTAATGAGTATCTGTCTGAGCTGGGCTTGCTTCTCAGCATATAACATTACCTTTGTTATTTATAATGGATATTTTGACACTTTATACAAAACAGATGTGTGTTATGGACAGTG[T/A]TCATTCATTATGAGCTTTCATTGGATAGTCACTGATCTGTTCATGTCTTTTATTTTTCCCTGTTTTCTGATCATCACTTTATATTTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGCTGGTAAATGTGTAACGGAGGGTTCAGTGAAGAGGAAATCTGAGAGTAAAGCTGCTCTGACTTTAGGAATCATTGTGTCTGTGTATCTGCTTTGCTGGATTCCATACTATATCTGTACATTAACTGTAAGCTCCTCCACAATTATAAATGTTTTGACATGGGTTGTCTATGCTAACTCAGGTCTGAATCCTCTGGTTTATGCTTTATTTTACCCCTCGTTTAAGAAGACATTTAAACACATTTTAACTCTGAAAATACTTCATTCTGCATCCTCTCTTATAAATATCTTTACAGAAAGTTAATTGTAATAATGTCATAATGTACTAAGTAATGTGCCAAGTCCTAAAAAAAGTCATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34976
Status:
Mutation detected in F1 DNA
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
ENSDART00000142464 Nonsense 222 340 1 1
ENSDART00000144014 Nonsense 194 295 2 2
Genomic Location (Zv9):
Chromosome 10 (position 41849971)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40562680
GRCz11 10 40483866
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCTGTTCATGTCTTTTATTTTTCCCTGTTTTCTGATCATCACTTTATA[T/A]TTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCT
Long Flanking Sequence:
TTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGTCTGTGGCTGATCTGCTTGTTGGATTCATCATGCCTGTAGAGGCCATCAGACTGACAGAGACATGTTGGTACTTTGGAGACACTTTCTGTTCACTCTATTTATTATATATTGCGGTACTTCTTTCTGCATCTCTTAGTAATTTTGTTTTAATTGCTCTTGATCGATATGTGGCTGTGTGTCACCCTTTACTGTACCCACAAAAAATAACCATCACTAAAACATTAATGAGTATCTGTCTGAGCTGGGCTTGCTTCTCAGCATATAACATTACCTTTGTTATTTATAATGGATATTTTGACACTTTATACAAAACAGATGTGTGTTATGGACAGTGTTCATTCATTATGAGCTTTCATTGGATAGTCACTGATCTGTTCATGTCTTTTATTTTTCCCTGTTTTCTGATCATCACTTTATA[T/A]TTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGCTGGTAAATGTGTAACGGAGGGTTCAGTGAAGAGGAAATCTGAGAGTAAAGCTGCTCTGACTTTAGGAATCATTGTGTCTGTGTATCTGCTTTGCTGGATTCCATACTATATCTGTACATTAACTGTAAGCTCCTCCACAATTATAAATGTTTTGACATGGGTTGTCTATGCTAACTCAGGTCTGAATCCTCTGGTTTATGCTTTATTTTACCCCTCGTTTAAGAAGACATTTAAACACATTTTAACTCTGAAAATACTTCATTCTGCATCCTCTCTTATAAATATCTTTACAGAAAGTTAATTGTAATAATGTCATAATGTACTAAGTAATGTGCCAAGTCCTAAAAAAAGTCATAATGTACAACCCGCCATTCTGGTATCATTCACAACTTCTGGCAGTGGAAACAATTACATACTGTACTGTACCAAATCGTACCGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7340
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000142464 Missense 303 340 1 1
ENSDART00000144014 Missense 275 295 2 2
Genomic Location (Zv9):
Chromosome 10 (position 41849729)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40562438
GRCz11 10 40483624
KASP Assay ID:
554-4311.1 (used for ordering genotyping assays)
KASP Sequence:
CTCCACAATTMTAAATGTTTTGACWTGGGTTGTCTATGCTAACTCAGGTC[T/A]GAATCCTCTGGTTTATGCTTTATTTTACCCCTCGTTTAAGAAGACATTTA
Long Flanking Sequence:
TCGATATGTGGCTGTGTGTCACCCTTTACTGTACCCACAAAAAATAACCATCACTAAAACATTAATGAGTATCTGTCTGAGCTGGGCTTGCTTCTCAGCATATAACATTACCTTTGTTATTTATAATGGATATTTTGACACTTTATACAAAACAGATGTGTGTTATGGACAGTGTTCATTCATTATGAGCTTTCATTGGATAGTCACTGATCTGTTCATGTCTTTTATTTTTCCCTGTTTTCTGATCATCACTTTATATTTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGCTGGTAAATGTGTAACGGAGGGTTCAGTGAAGAGGAAATCTGAGAGTAAAGCTGCTCTGACTTTAGGAATCATTGTGTCTGTGTATCTGCTTTGCTGGATTCCATACTATATCTGTACATTAACTGTAAGCTCCTCCACAATTATAAATGTTTTGACATGGGTTGTCTATGCTAACTCAGGTC[T/A]GAATCCTCTGGTTTATGCTTTATTTTACCCCTCGTTTAAGAAGACATTTAAACACATTTTAACTCTGAAAATACTTCATTCTGCATCCTCTCTTATAAATATCTTTACAGAAAGTTAATTGTAATAATGTCATAATGTACTAAGTAATGTGCCAAGTCCTAAAAAAAGTCATAATGTACAACCCGCCATTCTGGTATCATTCACAACTTCTGGCAGTGGAAACAATTACATACTGTACTGTACCAAATCGTACCGCTCAGTGGAAATGAACTGTTAAAGTAGTGTGGGGTAGCTGTAGCTGAAGTGGAGCACTCTGAAATAAAAGCAGCATATTAAATTTGGATGCTTTTCATGGACCTTTTACTTTGCCAGTTAGAGAGACACTTGCATTGAAGACAGGTGAATTCTTACAAGTACAGATGTGCTGATAAGACCTGGGCCTATAGGTTAAAATGTGTATACATCAGGAATCTGCAATGTTGTCATACAGCGGGGGAAGA
Associated Phenotype:
Not determined