Busch Lab

ZMP

si:ch211-139n6.10

Ensembl ID:
ENSDARG00000095395
ZFIN ID:
ZDB-GENE-091116-16
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 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21808 Nonsense Available for shipment Available now
sa34978 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21808
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
ENSDART00000132871 Nonsense 45 344 1 1
Genomic Location (Zv9):
Chromosome 10 (position 42072339)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40785048
GRCz11 10 40706234
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCATGTGTCAAAGGAAAACGCTCCATTTATGAATATATAGTCATGTA[T/A]GTGTTCTTTTCACTGCTGTCAGCATGGACTGTGTTTCTGAACCTGCTGGT
Long Flanking Sequence:
CAAAGTAGAGTCGCACTAGTCACAATTCAGCTGAGTGCACATAAGCTTACTTTGGTGTGCTACAAGAGTATTGCAGTATGTAATGTGGGTGGAGTATCACTGCTTAACCCTTCAGTTTAAAGCTCTTTACACCTTAAAAATAACCCAATAAAATAATTAAGAATGAATAAAATATAAATGTAGTATTTAGCTTGAAAAATAGAGAAGAAAAAGTATTGAAGATCAAAACAAGCTTGCATTACTATAGCAACTATAAACAGTAGACTGGGAGGATTTCTTATTGTTTAATCATTTATTTCTTTAACATTTGATTGGGCGATGAGTGATGCAGACACTGTATAAATGAAAGGACAGAAAGGAGAACAGAACAAACTCCTAACAGGAGGAGACTCACTCATGGCCTACGAGACAGAGGATCAGGAGACTCAATACTGCTTTCCTAACATCAACTCATCATGTGTCAAAGGAAAACGCTCCATTTATGAATATATAGTCATGTA[T/A]GTGTTCTTTTCACTGCTGTCAGCATGGACTGTGTTTCTGAACCTGCTGGTGATCATCTCCATCTCTCACTTCAAGAAGCTTCACACTCCAACCAACATGATTATTCTCTCTCTGGCGGTGGCTGATCTGCTTATTGGACTTATTGTGATGCCCATACAGGCCATCAGACTGATTGAGACATGTTGGTACTTTGGAGAAACTTTCTGTGGACTCAATTCAATAATAATTGGGGTGATCTTCTCAGCATCTTTCAGTAATTTAGTTTTAATTGCTGTTGATCGTTATGTTGCTGTGTGTCACCCTTTACTGTACCCACAGAAAGTAACCATGGCCAAAATGTTAATGTGTCTGTGTCTGTGCTGGCTTTACTACTCTGCTTATAACACTGCCTTTGTAATTAATAATGGATATTTTGACTCCTCACAAAGAACAGACATGTGTTATGGAGACTGTTTAGTCATGATGAGTTTTAGTTGGATACTCACTGATCTGTGCATGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34978
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
ENSDART00000132871 Nonsense 310 344 1 1
Genomic Location (Zv9):
Chromosome 10 (position 42073134)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 40785843
GRCz11 10 40707029
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTGGAATGGACTGTGCTCACTAACTCAGGTCTGAATCCTCTGATTTA[T/A]GCTTTATTTTATCACTGGTTTAAAAAGACAGCTAAGCATATTTTGACTTT
Long Flanking Sequence:
TGTCACCCTTTACTGTACCCACAGAAAGTAACCATGGCCAAAATGTTAATGTGTCTGTGTCTGTGCTGGCTTTACTACTCTGCTTATAACACTGCCTTTGTAATTAATAATGGATATTTTGACTCCTCACAAAGAACAGACATGTGTTATGGAGACTGTTTAGTCATGATGAGTTTTAGTTGGATACTCACTGATCTGTGCATGTCTTTTATTTTTCCCTGTGTCATTATGATCACTTTATATTTGAGGATTTTCTATGTCGTTCATCAGCAAGTGAAGGTTATAAACTCTCTGATGAAGGGTGGTAAATGTGTAACGGAGGGTTCAGTAAAGAGGAAATCTGAGAGTAAAGCTGCTCTGACTTTAGGAATCATTGTGTTAGTTTATCTGCTTTGCTATATCCCATACTATATCTGTACATTAACTGTTAACTCCTCCACAACTATAACTGTTTTGGAATGGACTGTGCTCACTAACTCAGGTCTGAATCCTCTGATTTA[T/A]GCTTTATTTTATCACTGGTTTAAAAAGACAGCTAAGCATATTTTGACTTTGAAAATATTTTACCCGGGTTCCTCTCTGATCAATATTTTTACAGAACATGAACTGTAATTTAACTTATAATCCCTCATATAGTTTCTAAAGAAAAAAAAGAGACAACATGGTTCCTTTTCTTCCTAACGTCTCCCTTTATTACACTGTGGGTCATTAGAGATGTTGGGGTACATAATGATCACCCTAGAAAATCATTGATGTATTAGGCTACTCATAATTTTATTGATTATTTGTATTTAGTAGTCATGTTTATATTTCCAATCCACTGGTCACACATGATAGTTGAACTTATTGTATTTGAGGCAGTGTTGCATTAATTCAGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTACAGTATTTTACACCTTCAATTAACGATTCAG
Associated Phenotype:
Not determined