ZMP

drd3

Ensembl ID:

ENSDARG00000032131

ZFIN ID:

ZDB-GENE-021119-1

Description:

D(3) dopamine receptor [Source:RefSeq peptide;Acc:NP_898890]

Human Orthologue:

DRD3

Human Description:

dopamine receptor D3 [Source:HGNC Symbol;Acc:3024]

Mouse Orthologue:

Drd3

Mouse Description:

dopamine receptor D3 Gene [Source:MGI Symbol;Acc:MGI:94925]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15862	Essential Splice Site	Available for shipment	Available now
sa6765	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15862

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
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Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039851	Essential Splice Site	268	454	6	8
ENSDART00000129675	Essential Splice Site	280	466	5	7
ENSDART00000130568	Essential Splice Site	286	472	6	8

Genomic Location (Zv9):

Chromosome 24 (position 21593421)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20840550
GRCz11	24	20984969

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CACACAAAGAGAAAAGAGACCTTTCCCCCATCAGGATCAATGTGATAACT[G/A]TGCGTATGCCATTGGGCGTCTGCATGCGTGTATAGAAATGCRTGTGACTA

Long Flanking Sequence:

TCAAAGTCACTTAAATCACCTTTCTTCCCCATACTGATGCTCGGTTTGAACTGCAGCAGATCGCCTTGACCATGTCTACATGCCTAAATGCATTAAGTTGGCATGGCAGATGTGATTGGCTGATTAGAAATTTGTGTTAACAAGCAATTGGACAGTAGTACCTAATAAAGTGGCCGGTGAGGGTATTTTATGTTTGTGAAATGCAAATATGAACTTGAATGTCATATATGTAATTTCCTTATATCAGATTTCTATATGCAATGCCAGTGAGCATGAGTGAAACTTCTTTTCCTTGTCTTGATTTCCCTGTCTTTTACATTTTAAAAGGCTGTGCTCCCCTCCCGTTTTTCTGGCTACAGAAATTTGCTTTACATGCTTCTGCATTGCTTTTGTTTTCCACCCTTTGACTCTTTAAGATCTCTCCACAGGAGATGTGTTTACAAGACGACGCACACAAAGAGAAAAGAGACCTTTCCCCCATCAGGATCAATGTGATAACT[G/A]TGCGTATGCCATTGGGCGTCTGCATGCGTGTATAGAAATGCGTGTGACTACTCTAATCTTGCATGAAATTAGTCTTCTCGGAGGAACAGACTCTGTAAAGAAATCTTACAAGGTATTTTGAGATAGCTGGCAGCTTTCTATTTTAGCATAGCGGGTGTGTTTCTTATCCCTGTGGCTGTATATGTGGCTCTGACGCACGGCTCTGGCTGGTACTCCACTTCTCTCACTGGTGATCTCTCTTTCCACGACAGTCACTTCAAACGTAACTTTGGAGTAACAAGCTTCAGTACTAAGGAGCCGTAGGACATGTCTATAGTGTAGCTGTTGGATGAGGCTTTGGATCAGAGCTGTGATTTAAAGAGAAGCGATATGGATTAATTGAAGATTTAGGGAAAAGGCTAAAGGCTCCTTTTACAAGCCGCCTAAACAGTTTAGCTTTGGCATTTTTTAATTCATTCATCCGGTCTCTGGGTCTGGGGGAAGCACTGTTAGCTTAGCTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6765

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000039851	Nonsense	396	454	8	8
ENSDART00000129675	Nonsense	408	466	7	7
ENSDART00000130568	Nonsense	414	472	8	8

Genomic Location (Zv9):

Chromosome 24 (position 21613980)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	20861109
GRCz11	24	21005528

KASP Assay ID:

554-4290.1 (used for ordering genotyping assays)

KASP Sequence:

TCMTGTCTATTTGTGTGTGTTNNTGTTTTGCAGGTGTTTTTCTTATTTGCTG[G/A]CTGCCTTTCTTTGTGACYCACATCCTCAACACTCATTGCAGAGCTTGTCA

Long Flanking Sequence:

TAAATGTACTTAAATATGGGATATGTGACAAATAAAGGCTTCTTTATCATCATCATCATATATACTTTGAAGACATTTCTTTAACAAAAGGTTATAAACAAACAAAAATATTTTGAATGCTCTCTTTTTTGGAATAAGAACTGTTAGCTCTTCATAATTGCTCTTTGTATTCTGGCATTTCAGTGTAACATTCAGGATTTTTTCAGGTTAAATTTAACTTTGCTAATAAAATGAATCATTTTTAAGATGGCAGTACTGTCATACTGTCAGCATTGAAACTCAAATTCTGGTTAAAATGTAAAGTTGGAGAGATATGTTCGTGCAGCTGAAGAAATAGAAAAAAAGGTTGGAAAATTACTTTGGAATATAACTTCCAGAATCAGAATTGGATGGTGAATCTCTATAGAATCCCACTATTGTACTCGGCAACTTTTATCATTTTAAAATCATTCATGTCTATTTGTGTGTGTTTGTTTTGCAGGTGTTTTTCTTATTTGCTG[G/A]CTGCCTTTCTTTGTGACCCACATCCTCAACACTCATTGCAGAGCTTGTCACATTCCTCCTGAGGTCTACAGCGCCTTCACTTGGCTCGGCTACGTCAACAGCGCTCTCAATCCCGTCATCTACACCACGTTCAACATCGAGTTTCGCAGAGCCTTCATTAAAATCCTGAGCTGCTAAACCATGGGCTATATTCCCATAAAACGTTTAATGCGGCTTTCAGACACTGTGGATGCCATTTTGGGATGCAATATGCCATACACAGAGGATATTAAAAGACTGTCTGAATGTGTTCAGGGGGATTTCACAGTCACTATAAAGCACACTACGCTTGCAATCGGTGGATAAGAATTGATTGCAATCTTCTTCAAGTTCACAGGAGAACCAGTTTGTGCTTCACATCCAACGTCAAAGCCTAGAAGATCTTTTTGTGTTCTCCATCTCAGCACCTTGTCGCATGTGGGCAAATCCAGAGTTCATTGTGTGTATGCATGTGTCTCACC

Associated Phenotype:

Not determined