Busch Lab

ZMP

taar20m

Ensembl ID:
ENSDARG00000092891
ZFIN ID:
ZDB-GENE-060413-8
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa18369 Nonsense Available for shipment Available now
sa27669 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa18369
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
Order Allele From EZRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000133729 Nonsense 117 343 1 1
Genomic Location (Zv9):
Chromosome 10 (position 41874313)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40587022
GRCz11 10 40508208
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTAAATGACAAGTGTTGGTACTTTGGACAAATATTCTGTGGACTCTATT[T/G]ATTATTTGTGTCATTACTCCTCTCAACATCTCTTGGTAATTTRGTTTTAA
Long Flanking Sequence:
GACTGGATTTTAGGTTAGCGTTCAGCAAACCAACAGGAGAAACTTAAAAAAAATAAAAAACATTTTGATAGATTACATCAGAGTGGGCGGTAGATGGGTTGGTCAGTCTATTCCAGACTCTGTATAAATAAAAGGACAGAAAGGAGAGCAGAACAAACTCCTAACAGGAGGAGACTCACTCATGGCCTACGAGACAGAGGATCAGGAGACTCAATACTGCTTTCCTGACATCAACTCATCATGTGTCAAGGAACAACGCTTAAGAAATAGATTTAAAATAACATATTTGCTGGTGTCATTGCTGTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGGCTGTAACTGATCTGCTCATTGGATTCATCATGCCTATAGAGGCCATCAGACTAAATGACAAGTGTTGGTACTTTGGACAAATATTCTGTGGACTCTATT[T/G]ATTATTTGTGTCATTACTCCTCTCAACATCTCTTGGTAATTTGGTTTTAATTGCTGTTGATCGTTATGTGGCTGTGTGTCACCCTTTACTGTACCCACAGAAAATAACCACGGCTAAAATGTTAATGAGTATCTGTCTGAACTGGATTTGCATATCAGCTTATAACACTACCCTTGTAGTTAATAATGGACATTTTGACACTTCACACAGAATAGATGAGTGTCACGGGGAATGTTTATTCATGATAAGTTTTAGTTGGATAGTCATTGATCTGTGCATTTCTTTAATTTTTCCTTGCACTCTGATCATGGTGTTATATTTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGGTGATAAGTGTGTAACAGAGGGTTCAGTGAAAAAGAAATCTGAAATTAAAGCTGCTCTGACATTAGGAGTTATGGTGTCAGTTTATCTGCTTTGCTATATCCCGTACTATATCTGCTCTCTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27669
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
ENSDART00000133729 Nonsense 246 343 1 1
Genomic Location (Zv9):
Chromosome 10 (position 41873925)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40586634
GRCz11 10 40507820
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGGTGATAAGTG[T/A]GTAACAGAGGGTTCAGTGAAAAAGAAATCTGAAATTAAAGCTGCTCTGAC
Long Flanking Sequence:
ATTCTCTCTCTGGCTGTAACTGATCTGCTCATTGGATTCATCATGCCTATAGAGGCCATCAGACTAAATGACAAGTGTTGGTACTTTGGACAAATATTCTGTGGACTCTATTTATTATTTGTGTCATTACTCCTCTCAACATCTCTTGGTAATTTGGTTTTAATTGCTGTTGATCGTTATGTGGCTGTGTGTCACCCTTTACTGTACCCACAGAAAATAACCACGGCTAAAATGTTAATGAGTATCTGTCTGAACTGGATTTGCATATCAGCTTATAACACTACCCTTGTAGTTAATAATGGACATTTTGACACTTCACACAGAATAGATGAGTGTCACGGGGAATGTTTATTCATGATAAGTTTTAGTTGGATAGTCATTGATCTGTGCATTTCTTTAATTTTTCCTTGCACTCTGATCATGGTGTTATATTTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGGTGATAAGTG[T/A]GTAACAGAGGGTTCAGTGAAAAAGAAATCTGAAATTAAAGCTGCTCTGACATTAGGAGTTATGGTGTCAGTTTATCTGCTTTGCTATATCCCGTACTATATCTGCTCTCTAACTGTAACCTCTTCCACAACTCTAAATGTTTTGATTTGGACCTTGCATGCTAACTCAGGTCTGAATCCTCTAGTTTATGCTTTATTTTATCGCTGGTTTAAAAAGACAGCTAAACTCATTTTAAATTTGAAAATATTTCTGCCAGCATCCTCTCTGATCAATATTTTTTCACAACATGAATGATCAATACTTGCAAAGCTGTCACAAATAAAGGCAGATAAAACAGTTTTTAGTTTTTATTTGTAGTTTTCACTGCTCATGTTATATCGCACATACTGTAGTATAAAGTAACATGCATAAAAAGATGCTTAAGTAACTTATAATGTACTGCTGCAAATGCAAAAAGAAAGATATGTGACTGACAGCAATATGCACTGCACAGTAATATC
Associated Phenotype:
Not determined