Busch Lab

ZMP

taar18a

Ensembl ID:
ENSDARG00000054254
ZFIN ID:
ZDB-GENE-100514-5
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
sa41723 Nonsense Mutation detected in F1 DNA Not yet available
sa41722 Nonsense Mutation detected in F1 DNA Not yet available
sa21802 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa41723
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
ENSDART00000030565 Nonsense 114 345 1 1
Genomic Location (Zv9):
Chromosome 10 (position 41890505)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40603214
GRCz11 10 40524400
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCCGTCAAGTTGATTGAGACATGTTGGTATTTTGGAGACATTTTGTG[T/A]GACCTGTATATGATTATCATGGGACTTCTCCTCTCAGCATCTCTTAGTAA
Long Flanking Sequence:
GTTTTCATTTCTGGCTTATTTTCTCTGGAATTTGTCTACCATTTTTAAATTTATTATGAAAATGAAAATGATTTATTATGCATCATCAGAGTGGGCGGTAGATGGGTTGGTCAGTCTGATCCAGACACTGTATAAATGAAAGGACAGAAAGGAGAGCAGAACAAACTCCTAACAGGAGGAGACTCACTCATGGCCTACGAGACAGAGGATCAGGAGACTCAATACTGCTTTCCTGACATCAACTCATCGTGTGTGAAGGAAAATCGCTCCAAACATGAATACAATATCATGTATGTGTTCTTTTCATTGCTGTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGGCAGTAAATGATCTGCTTCTTGGACTTATAGTGATGCCTGTTGATGCCGTCAAGTTGATTGAGACATGTTGGTATTTTGGAGACATTTTGTG[T/A]GACCTGTATATGATTATCATGGGACTTCTCCTCTCAGCATCTCTTAGTAATTTAATTTTAATTGCTGTTGATCGTTATGTGGCTATTTGTCACCCTTTATTGTACCCACAGAAAATAACAATGACTAGAACTTTAATTAGCATCTTTGTCTGCTGGTTTGTCTGCTTGACTAACAATATTGCTTTTCTAGTTAGTAGCAGACATTTTGACATTTTGCAAAAAACAAACATGTGCCATGGACAATGCACTTTGATTGTAAGTTTTTCATGGACTTTTACTGACCTCTTCCTTTCCTTCCTAGTACCCTGTACTCTGATTATAACTTTGTATTTGAGAATATTTTATGTTGCTTATCAGCAAGTAAAAGTTATCAATGCTATTATAAAGGGTGGTAAATGTGCAGTGGAGGGTTCAGTGAAGCGGAAATCTGAGCGCAAAGCTGCTCTCACATTAGGAATTGTTGTGACAGTTTATCTACTTTGCTATATTCCCTACTATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41722
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
ENSDART00000030565 Nonsense 306 345 1 1
Genomic Location (Zv9):
Chromosome 10 (position 41889929)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40602638
GRCz11 10 40523824
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCTTCCACGATGAAAATTCTGATTTGGTCTTTGTACATTAACTCCTG[T/A]CTAAATCCTCTGATCTATGCTTTATTTTATCGCTGGTTTAAAATATCAGT
Long Flanking Sequence:
TATGTGGCTATTTGTCACCCTTTATTGTACCCACAGAAAATAACAATGACTAGAACTTTAATTAGCATCTTTGTCTGCTGGTTTGTCTGCTTGACTAACAATATTGCTTTTCTAGTTAGTAGCAGACATTTTGACATTTTGCAAAAAACAAACATGTGCCATGGACAATGCACTTTGATTGTAAGTTTTTCATGGACTTTTACTGACCTCTTCCTTTCCTTCCTAGTACCCTGTACTCTGATTATAACTTTGTATTTGAGAATATTTTATGTTGCTTATCAGCAAGTAAAAGTTATCAATGCTATTATAAAGGGTGGTAAATGTGCAGTGGAGGGTTCAGTGAAGCGGAAATCTGAGCGCAAAGCTGCTCTCACATTAGGAATTGTTGTGACAGTTTATCTACTTTGCTATATTCCCTACTATATATTGTCTGTTATAGGGACCACAGTAATATCTTCCACGATGAAAATTCTGATTTGGTCTTTGTACATTAACTCCTG[T/A]CTAAATCCTCTGATCTATGCTTTATTTTATCGCTGGTTTAAAATATCAGTTAAATGCGTCTTAACTCTTAAAATATTAGAGCCAGCTTCCTCACTCTTAGATATTTTTAAAGATAATTCATGAATAGGGCTTTCTTTTTCTTTCTTTCTTTCTTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTATATATTTATCTAAAACATATGTTTATTCATTCATTATTTGATTTACATTTTGAAAAGGGCCAAGTTGAAACTAATCAAACTTGTATTTGTAAGGAATTTAATACTTGTGGTTTCTTCTGGACTCCATTTCCAAATGTCTTTTACATTGGGTACCAATAACTCACAAACATGTACATATTGTAGGCCCACACAAATTCTTTTTATTTACTTGTGTGAATATGTGTAAACTTAAATTGTAAACTTTTAGTTTTTAAATGTATTTTTGTAATATTATTTATTAATATGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21802
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
ENSDART00000030565 Nonsense 312 345 1 1
Genomic Location (Zv9):
Chromosome 10 (position 41889911)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40602620
GRCz11 10 40523806
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTGATTTGGTCTTTGTACATTAACTCCTGTCTAAATCCTCTGATCTA[T/A]GCTTTATTTTATCGCTGGTTTAAAATATCAGTTAAATGCGTCTTAACTCT
Long Flanking Sequence:
CCTTTATTGTACCCACAGAAAATAACAATGACTAGAACTTTAATTAGCATCTTTGTCTGCTGGTTTGTCTGCTTGACTAACAATATTGCTTTTCTAGTTAGTAGCAGACATTTTGACATTTTGCAAAAAACAAACATGTGCCATGGACAATGCACTTTGATTGTAAGTTTTTCATGGACTTTTACTGACCTCTTCCTTTCCTTCCTAGTACCCTGTACTCTGATTATAACTTTGTATTTGAGAATATTTTATGTTGCTTATCAGCAAGTAAAAGTTATCAATGCTATTATAAAGGGTGGTAAATGTGCAGTGGAGGGTTCAGTGAAGCGGAAATCTGAGCGCAAAGCTGCTCTCACATTAGGAATTGTTGTGACAGTTTATCTACTTTGCTATATTCCCTACTATATATTGTCTGTTATAGGGACCACAGTAATATCTTCCACGATGAAAATTCTGATTTGGTCTTTGTACATTAACTCCTGTCTAAATCCTCTGATCTA[T/A]GCTTTATTTTATCGCTGGTTTAAAATATCAGTTAAATGCGTCTTAACTCTTAAAATATTAGAGCCAGCTTCCTCACTCTTAGATATTTTTAAAGATAATTCATGAATAGGGCTTTCTTTTTCTTTCTTTCTTTCTTTTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTATATATTTATCTAAAACATATGTTTATTCATTCATTATTTGATTTACATTTTGAAAAGGGCCAAGTTGAAACTAATCAAACTTGTATTTGTAAGGAATTTAATACTTGTGGTTTCTTCTGGACTCCATTTCCAAATGTCTTTTACATTGGGTACCAATAACTCACAAACATGTACATATTGTAGGCCCACACAAATTCTTTTTATTTACTTGTGTGAATATGTGTAAACTTAAATTGTAAACTTTTAGTTTTTAAATGTATTTTTGTAATATTATTTATTAATATGAAAATATGTATATGATTTATGC
Associated Phenotype:
Not determined