ZMP

gpr89b

Ensembl ID:

Human Orthologues:

GPR89A, GPR89B, GPR89C

Human Descriptions:

G protein-coupled receptor 89A [Source:HGNC Symbol;Acc:31984]
G protein-coupled receptor 89B [Source:HGNC Symbol;Acc:13840]
G protein-coupled receptor 89C [Source:HGNC Symbol;Acc:31985]

Mouse Orthologue:

Gpr89

Mouse Description:

G protein-coupled receptor 89 Gene [Source:MGI Symbol;Acc:MGI:1914799]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa34549	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa27337	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa34549

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115404	Essential Splice Site	105	455	4	14

Genomic Location (Zv9):

Chromosome 9 (position 5954847)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	5936143
GRCz11	9	5914128

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGTGCCTTTCTACATTGGCTACTTTGTGGTCAGTAATATACGTTTATG[T/C]AAGTATATTTGTCTTTTTATATTCTGTAAGCTTTTCTACTAGTTTGCTCA

Long Flanking Sequence:

ATGTTTGGTTGTGATGGTGTAAGAGACACTCCAACTAACATGTTTTATTTATTTTTTCTGTACACAGGTGCTGTTTTTTGGATTTGGGTGGCTGTTTTTCATGCGTCAGTTGTTTAAAGATTATGAGGTATGATGCACAAGATTGCAGATTTGGAGCAGTTTGTTACTTTACAGGTGCAGCGTCAGTGATGTGTCTCTTTCTTCATCAGGTTCGGCAGTATGTGGTGCAGGTGGTGTTCTCCATCACGTTCGCCTTCTCTTGCACAATGTTTGAGCTCATTATCTTTGAGATCCTCGGTGCATTGAGCAGCTCGTAAGTGTTTTGTGAAAATTTTGGGGGGCTCCATTTATGAGATACGTAGATCAAATATTGACATTCTTTTTGTAAACAGGTCCAGGTATTTCCACTGGAAGCTGAATTTGTATGTAATATTGCTGGTTCTGATATTTGTGGTGCCTTTCTACATTGGCTACTTTGTGGTCAGTAATATACGTTTATG[T/C]AAGTATATTTGTCTTTTTATATTCTGTAAGCTTTTCTACTAGTTTGCTCACAGCTTTCTCCTATATATTTCTCATATTTGTTTTCTTCGCTCTTACAGTGCAGAGACAGAGGTTGCTTTTTTCATGTGTGGTCTGGTTTACATTCATGTATTTCTTTTGGAAACTGGGCGATCCTTTTCCTATACTCAGTCCCAAACATGGTAGGCTATTTTTGTTTTTTAATACAAAACCTTTTAAAACTCTGGTTACTTTTTTTTCTATTTTTTATGCATATATGAATAATACAGATGTTTTTGAGTAACTAAATTGAAATTACACATTATTGCTCCTTTGCTAATTTTGATAGCTAATGAAATCTCCATGTTAATTTCTGCTTAAATTGCTCTTGGGTGCGTTTCTCAAAACCATCGTTAGCCAACTAAGGTCGCAAGTTCCGTCATTACAAACATAGTTTGTTGATTTGCCGTTTCCCCAAATCCGTCGCTCCAACAAACATTCGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27337

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
ENSDART00000115404	Nonsense	329	455	11	14

Genomic Location (Zv9):

Chromosome 9 (position 5945524)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	5926820
GRCz11	9	5904805

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGGGAAGACTGACCCGGTGACGAGGGGAATCGAGATCACCGTCAACTA[T/A]CTTGGAATTCAGTTTGATGTATGTATATGTATATTTGGCTGAATATTTTA

Long Flanking Sequence:

TGTATAGTATCATATACAAAATATTAATTTGAGAGAGATGTTAGCGAGGGGTGTACTCATGTACGCTGAGCCCTGTATGTAGTTTTTTATTCCAGCCAAATCAAAATAATTTATACTTACTCCAATGTAAAAAAGACAATAGGAAAAAAAATTAATAATGCCTTTGCTCTGTTAAATATAATTTGGGAAGTATTTGAAAAAGAGTTCAATTCAATACTGAATTTTAATATATAAATATCTTATGTTGTTGCATTCCCAGGAGCGGATAGAATACTCAAAAACATTTCAAGGGAAATACTTTAACTTCTTAGGGTATTTCTTCTCCATCTACTGTGTGTGGAAAATATTCATGGTAAGTGTCAATATTTTTGGCATACACTTTAACATTATTAGAATGCCCTTTAATTGTTTTGTTTTTAATAGGCCACTATAAACATAGTGTTTGACCGTGTGGGGAAGACTGACCCGGTGACGAGGGGAATCGAGATCACCGTCAACTA[T/A]CTTGGAATTCAGTTTGATGTATGTATATGTATATTTGGCTGAATATTTTAAGCTTTTGCATATTACATTATATTGCATGCATATATTACATTGTTAGTTCTGATTTGTTGTTTTTCTTTTTTTATATTGGTTCACATTTTTACAAAATAAATATTTGTATATTATTATTATTAAGTCATATTAACAATAACTAATAATAACAAAGCTGGATTAATAAATTAAAAGAGATGTTGGGCTTCTCAAAGCAATAGTAATGTAACTAGTAAAATTATACTAACAAATCACATTTTTTTTACTGTTATTTAATTCAGACTAAAACACAATTTGAAAATATCAAATAAGCAAACCAGTTTTGTTCCGTTTTAATTAATTAGACAACAATTGTGAAGTCTAGGGGTCTGTTCTTCATACGTACGTGGATTACTCAATTATCTGGATTTGGTTATTGAGGATTTGACATGATCCAGCATTGTTCGTTCTTCACAGCTCATCCGGTCTGG

Associated Phenotype:

Not determined