ZMP

si:ch211-26a17.7

Ensembl ID:

ENSDARG00000039349

ZFIN ID:

ZDB-GENE-090313-105

Description:

Novel protein similar to H.sapiens GPR103, G protein-coupled receptor 103 (GPR103) [Source:UniProtKB

Human Orthologue:

QRFPR

Human Description:

pyroglutamylated RFamide peptide receptor [Source:HGNC Symbol;Acc:15565]

Mouse Orthologues:

C130060K24Rik, Qrfpr

Mouse Descriptions:

RIKEN cDNA C130060K24 gene Gene [Source:MGI Symbol;Acc:MGI:2441881]
pyroglutamylated RFamide peptide receptor Gene [Source:MGI Symbol;Acc:MGI:2677633]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24937	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38948	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42220	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24937

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041026	Nonsense	16	355	1	6
ENSDART00000133049	Nonsense	16	295	1	5

Genomic Location (Zv9):

Chromosome 13 (position 30439613)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	30085561
GRCz11	13	30216011

KASP Assay ID:

554-7383.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATACATGGGGGATAAGAAGATTACTCCTGAAGTGCTGGAGCAACTACTG[C/T]AGTTTTACAATCTTACCCGTCAGGAGTTCATCGAGACGTACCAGATCGAG

Long Flanking Sequence:

TTAAATGAATTTAGCTGATTAAATTAAGGTTATTGTTTTTATTATTTCATTTTTATAGCAACTAACAGTTGTAATAATGACGACAATTATGTTATTAGTAGTTTACATTGTCATTGAATTATATTTATAGGCTTTATTCCGTATTTTCTTTACCTATTTAATTTCGTTTGTTTTTTATTAAATAAACAAATTGTAACCTGGGCTACATCTCATCCATTCTTGAAGTGTCGAATTCCAGTGATTCGTTTTCAAACTCAGTGTGTTGTACAGCGTGTTTAGACAGCGAGTGTGAAATACTCAAACAGGTGTAGAGACACAGCCGATGTGTCAGAAGAAATACTCCGCATACTCCTGCTGCTGATTCAGTGTGAAGAGGCGCGAAGAGCAGAACTGACTAACAACAGCTGTAAAACTTTGATTTCTTTCTGGTCCCATTTCAAAGACGAGCATTATACATGGGGGATAAGAAGATTACTCCTGAAGTGCTGGAGCAACTACTG[C/T]AGTTTTACAATCTTACCCGTCAGGAGTTCATCGAGACGTACCAGATCGAGCCGCTGGTTTACATCCCGGAGTTGCCCGCTGGCGCCAAAACTACGTTTGTTATCGTGTACACGGTGATTTTTCTGCTGGCTCTCGTCGGAAACAGTGTCGTTGTGTATATTGTGTTAAGAAAGCGAGGGATTCAGACCGCCACAAATATCTTCATCTGCTCTCTAGCCGTCAGCGACCTGCTCATCTCTTTCTTCTGCATCCCATTCACTCTCCTGCAGAACATCTCTTCTGAATGGTTCGGCGGTGAGTATCACTTAAAACGGTGCATCGCTGTGATGTTGTTGTCGTTGAAAACTTTTAGGGTTGATTTCATTCTAATTAATCTGTTAAATGATGATGATGAAATAATGACTGATTGATGAATTTGATAACTACTAGGCTATTCCAGTGTCTTAATGATAGGGTAGTTCATGGTATTGATCAAATAATAATAGCCATATCATAAAATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38948

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041026	Essential Splice Site	266	355	None	6
ENSDART00000133049	Essential Splice Site	266	295	None	5

Genomic Location (Zv9):

Chromosome 13 (position 30448825)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	30094773
GRCz11	13	30225223

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAATACACAACTGTACGTAAATGATGTACCTAATCCCTCTTTATGCTTC[A/T]GAAAGAAGCGAAGAGCAATCAAGATGATGGTCACCATTGTCGTGCTGTTT

Long Flanking Sequence:

GATATTATCTTGGCACTCTTTAGACCCATTAGTACCAATTGAGCATTGTGTCAATGCCACAGCCTAGCTGAGTATTGTTGCTGACCATGTCCATCCCTTTATAACCACAGTGTACCCATCGTCTGATGGCTAATGTAGCGCCATGTCATGAAGCACGAATCATCTCAGACTGGTTTCTTGAACATGACTGCTCAAATGGCTCAAATAGCTTTGATATCTGGTGGAGCGCGAGATTTGCATCATGGATGTGGAGCCAAAAAATGAGCAACTGCATGATGCTATCATGTCAATATGGATCAAAATCTCTAAGAAATATTTCCAGCGCCTTGTTGAATCTATGCCACAAAGGATTAAGGCAGTTCTGAAGGCAAAAGGGGCTCCAACCAGGTAATAGTAAGGTGTACCTAATAAAGTGGCCGGTAAGTGTAAGTGTTAGCATATATCAGATAGAAAATACACAACTGTACGTAAATGATGTACCTAATCCCTCTTTATGCTTC[A/T]GAAAGAAGCGAAGAGCAATCAAGATGATGGTCACCATTGTCGTGCTGTTTACTGTCTGCTGGGCTCCCTTTCATACAGTTCACATCCTGTTTGAGTACAGTAAGAACATTTCAGTGTTCAGTAAAATATCTGTGCATTTTACAGTCCTCTTAACTCTCCTGTTTACTTGTTTTTGTTTTCAGGTTACCTGAACAAGAAGTATGATGACGTCACAGTTAATATGATTATAGCTGTCGCACAGGCCATAGGCTTTTCAAATTCATTCAACAATCCCATTATCTATGCTTTTATGAATGAAAACTTCCAGAAGAACTGCATGTCCACGCTTTCTGTTTGCATTAGGAGGTCCAGCCACCGTGTGGACGTAAAGGACAAATCAAAAGTGCTTTTTTGTAAGTCTGCCAGGCAAGATGAAGAGATCTCCGTCATGCCTAGAATACATATAATCGATCAGGTGCAATACGCAAGATCAAACATGCGAACGTCTATGTCATTTCTAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42220

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041026	Nonsense	340	355	6	6
ENSDART00000133049	None	None	295	None	5

Genomic Location (Zv9):

Chromosome 13 (position 30449130)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	30095078
GRCz11	13	30225528

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAATTCATTCAACAATCCCATTATCTATGCTTTTATGAATGAAAACTTC[C/T]AGAAGAACTGCATGTCCACGCTTTCTGTTTGCATTAGGAGGTCCAGCCAC

Long Flanking Sequence:

CTAAGAAATATTTCCAGCGCCTTGTTGAATCTATGCCACAAAGGATTAAGGCAGTTCTGAAGGCAAAAGGGGCTCCAACCAGGTAATAGTAAGGTGTACCTAATAAAGTGGCCGGTAAGTGTAAGTGTTAGCATATATCAGATAGAAAATACACAACTGTACGTAAATGATGTACCTAATCCCTCTTTATGCTTCAGAAAGAAGCGAAGAGCAATCAAGATGATGGTCACCATTGTCGTGCTGTTTACTGTCTGCTGGGCTCCCTTTCATACAGTTCACATCCTGTTTGAGTACAGTAAGAACATTTCAGTGTTCAGTAAAATATCTGTGCATTTTACAGTCCTCTTAACTCTCCTGTTTACTTGTTTTTGTTTTCAGGTTACCTGAACAAGAAGTATGATGACGTCACAGTTAATATGATTATAGCTGTCGCACAGGCCATAGGCTTTTCAAATTCATTCAACAATCCCATTATCTATGCTTTTATGAATGAAAACTTC[C/T]AGAAGAACTGCATGTCCACGCTTTCTGTTTGCATTAGGAGGTCCAGCCACCGTGTGGACGTAAAGGACAAATCAAAAGTGCTTTTTTGTAAGTCTGCCAGGCAAGATGAAGAGATCTCCGTCATGCCTAGAATACATATAATCGATCAGGTGCAATACGCAAGATCAAACATGCGAACGTCTATGTCATTTCTAGAGGAGAGAATGTCTGTGGAGAACAATAGGATGCATGCAGGATGTATTAGAGACTGATCTATAATTATATACATCTATGTATATATCAAATGTTTTAAAAAGAAGTTTCTCATGATAACCAGGGCTGCATTTATTTCACTAAAAATACTGTAAAAACAACACAAATATTGAGAAATATTACTACACTAACAGTAACTCAAACTATTTTTATTATATTTTAAAAAAATAATGTATTCCTGTGAAAGCAAAGCTGAAAGATGAGCAGCCTTCATCAGAGTTTCAGTATCACGTGATCCTTCAGAAATC

Associated Phenotype:

Not determined