ZMP

taar12b

Ensembl ID:

ENSDARG00000041454

ZFIN ID:

ZDB-GENE-041014-69

Description:

trace amine associated receptor 12b [Source:RefSeq peptide;Acc:NP_001076573]

Human Orthologue:

TAAR2

Human Description:

trace amine associated receptor 2 [Source:HGNC Symbol;Acc:4514]

Mouse Orthologues:

Taar2, Taar3

Mouse Descriptions:

trace amine-associated receptor 2 Gene [Source:MGI Symbol;Acc:MGI:2685071]
trace amine-associated receptor 3 Gene [Source:MGI Symbol;Acc:MGI:3527427]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37150	Nonsense	Available for shipment	Available now
sa37151	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37150

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
ENSDART00000060773	Nonsense	201	337	1	1

Genomic Location (Zv9):

Chromosome 20 (position 46224648)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	46197325
GRCz11	20	46101045

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACTGTGTGGGAAGTTGTATTGTGCTTTTTAACAAAGAGTGGGCTGTATA[T/A]CCATTCCTTACATTCTTTATTACCGGGGCCATCATGAGCTCTCTGTATAT

Long Flanking Sequence:

TTGTATGTTTGCCTGTTGCTGATGATCCTCACCACAGTGTTTGGGAACCTGCTGATCATCATCTCCATCTCTCACTTCAAACATCTGCAGTCTCCAACTCATCTGATCGTTCAGTCTCTTGCAGCCTGTGATTGTCTCATGGGCTCTTTGGTCATGCCGTACAGCATGGTGCGATCTGTTGAAGGCTGCTGGTATCTGGGAGATGTTGTGTGTAAAGTTCATTCTAGTTTGGACATGACTTTCTGTATGTCATCTTTACTACATCTCGGTTTAATATCTGTGGACAGGTACTGGGCCATTTGTGACCCTCTGAGATACAGATTAAGGGTCACAAACACCACAGTGACTGTATTTATCATCGTCATATGGCTGTTTTCATTTATCTACAACTTTTCAATTGTGTTTTCAGGAATAACTGCAGTTGGACTTGAGATGCTCATATTGCAGACTTACTGTGTGGGAAGTTGTATTGTGCTTTTTAACAAAGAGTGGGCTGTATA[T/A]CCATTCCTTACATTCTTTATTACCGGGGCCATCATGAGCTCTCTGTATATGAAAATCTTCCATGTTGCACAAAAACATGCAAAGGTTATGTCAGAAAGAGTGACTGGAGGGTTGAAGAGCCAAAGCTCTGCTCAGAGAGAGAGAAAAGCTGCTAAAACTCTGGCCATTGTCATGGGGGTCTTCATGTTCTGCTGGCTGCCGTATTGTGCTTTTACTGCTCTCTACCCTTTTTTCACCTTTTTAAATTCTGCTGAAGTTTTTGATGTTTTATTTTGGTTTGCGTATTTTAACTCCAGTTGTAATCCTGTGATCTATGGATTTTTCTATCCTTGTTTTCAGAAAGCCTTCAAGATTCTTATATCTACTTATATATTTGGAATCAGAAATGCAAACACATCAACATATGAATGAATACAACTGCTCCGCTTATGGCTGGATCACCATAAATATTTATTTCTATGTATGTATTTGTGTTTCATATGATGTATTTTATTATGAGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37151

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
ENSDART00000060773	Nonsense	296	337	1	1

Genomic Location (Zv9):

Chromosome 20 (position 46224933)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	46197040
GRCz11	20	46100760

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCTTTTTAAATTCTGCTGAAGTTTTTGATGTTTTATTTTGGTTTGCGTA[T/A]TTTAACTCCAGTTGTAATCCTGTGATCTATGGATTTTTCTATCCTTGTTT

Long Flanking Sequence:

AGGTACTGGGCCATTTGTGACCCTCTGAGATACAGATTAAGGGTCACAAACACCACAGTGACTGTATTTATCATCGTCATATGGCTGTTTTCATTTATCTACAACTTTTCAATTGTGTTTTCAGGAATAACTGCAGTTGGACTTGAGATGCTCATATTGCAGACTTACTGTGTGGGAAGTTGTATTGTGCTTTTTAACAAAGAGTGGGCTGTATATCCATTCCTTACATTCTTTATTACCGGGGCCATCATGAGCTCTCTGTATATGAAAATCTTCCATGTTGCACAAAAACATGCAAAGGTTATGTCAGAAAGAGTGACTGGAGGGTTGAAGAGCCAAAGCTCTGCTCAGAGAGAGAGAAAAGCTGCTAAAACTCTGGCCATTGTCATGGGGGTCTTCATGTTCTGCTGGCTGCCGTATTGTGCTTTTACTGCTCTCTACCCTTTTTTCACCTTTTTAAATTCTGCTGAAGTTTTTGATGTTTTATTTTGGTTTGCGTA[T/A]TTTAACTCCAGTTGTAATCCTGTGATCTATGGATTTTTCTATCCTTGTTTTCAGAAAGCCTTCAAGATTCTTATATCTACTTATATATTTGGAATCAGAAATGCAAACACATCAACATATGAATGAATACAACTGCTCCGCTTATGGCTGGATCACCATAAATATTTATTTCTATGTATGTATTTGTGTTTCATATGATGTATTTTATTATGAGCTGTTTGCATTTGAATGAACTGTAAATATCCTACAATCATGGGATTTTGTTAGCATTTTTAAATTCCCTTAATACGTTAAACTTAAACTGGATCATACTTTAATAGGTTTGCATTTATATGTGCTTCTTTTAGAGAAACATTGACATTTTAGCAGTTTGTTTGAGATAATTTTTTTAATTTTAATTTTGAAAAATGTTTTTCTGATTTAGGATCTGGGTGATTAAGTGAAGTCTGACTACATTTACATGTACTCAAATATTACATTTATTTCCAATAATCAGAGTA

Associated Phenotype:

Not determined