ZMP

ENSDARG00000068422

Ensembl ID:

ENSDARG00000068422

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35378	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38911	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35378

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098961	Nonsense	30	358	1	6

Genomic Location (Zv9):

Chromosome 12 (position 49152192)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	47925447
GRCz11	12	47899408

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAACTCCTGCAGTACTATAACCTCTCCCGGCAGGAATTCATCGACACCTA[C/A]AACATCCAGCCGCTGGTCTACATCCCTGAGCTCCCCGCCGGAGTCAAAAG

Long Flanking Sequence:

CAAATACGATTTGAAATGTGTTGAAGAAATCTGCTCTCCGTTAAACAGAAATTGGGGGGGTGGGGGGGGGGGAATAATTCAGCTGTAAATACTAATAGCTCAAAAACACTGAAGTATTATTCATGTCGGCACATTTTGGTAACTAAAAACGTGACTAGGATTATAAATAAAAGCACCCTCTTCTGCTAATAAACCAGTTTTAAACCTTTTTGTGTACACACTTGCGAACGCGCAATGACGCACGCTCCCTCATAATCGCGCGCGCGGGAAGCAGACGGCGGGAAACATCCCGAGAGGTGCAGCGCTGACGGATTTTATCACACTTCTCTAAAGTCACATCTGGATCTACTTTTTCCTTCTGTATGTGATCGATATAAACAACTCCTCGACATGTCTTCTTCCTCCACGGAGATGACAGCGACCACCAAAATCACTCCTGAGGTTCTCCAGGAACTCCTGCAGTACTATAACCTCTCCCGGCAGGAATTCATCGACACCTA[C/A]AACATCCAGCCGCTGGTCTACATCCCTGAGCTCCCCGCCGGAGTCAAAAGCACGTTTGTGGTGATGTACGTGATTATTTTCGTGCTGGCGCTGGTGGGGAACAGTTTGGTGGTGTATGTGGTGGTTCGGAAGCGCGCCATCAGGACCGCCACCAACATCTTCATCTGCTCGCTGGCTGTCAGCGACCTGCTCATCACCTTCTTCTGCATCCCCTTCACTCTGCTGCAGAACATCTCGTCCGAGTGGCTGGGAGGTCAGAGAATCTTCCATAACACTTTGATTAGTCGATAATTAACACGACAGGACAGTTTGACGGCTGGCAGAAGGAAACTAAATACGATAGCAACCAATACTGTATATAGTTTTGTTATGATAATTCTATGGTAATGCGGCAACTTTAACGTTAGTAATATAAACAAATGACTCATCACTGTCGTTTTATACAACTATATATTTTATATTAAGGTTTTATTGTAGTTTACTGTAGTAAAAACTAAAGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38911

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000098961	Essential Splice Site	270	358	5	6

Genomic Location (Zv9):

Chromosome 12 (position 49128124)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	47809787
GRCz11	12	47875340

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGAATGACCTGTGGTGATTGAACAGAATCATACCTGTGTGGTTCAAACA[G/T]GAAGAAGAAACGAGCTGTAAAAATGATGATCACCATCGTCCTGCTGTTCA

Long Flanking Sequence:

AAACATGAAGAAAAAGTGCACTATAATATTTGCAGATTTGATCTAGACTTGCTTGTTTAACTGCATTTTACTTTCAAAAGGTTGATTTATTTCATCTTTCAGTAGTATAACTGTGGTTGCAATTATTCATAAAATGAAAGCATTAGAATACCCATTAAAACACTCTAATGCAAAGCTTCAAGTGCTACTGATATCTTGAAATCAGAAACGTTAGATAATCAGAATGCACTGTGTGAACGCTGTGGAGCAAAGATCTCAAACTCAATTCCTTGAGGACTGCAGCTCCGCACAGTTTAGCTCCAACCACATCCCACCCACACATGCTTAATAGTCTACAGTAGTATTGAACACCATGATTATTTGGATTAGCTGTGTTTGATTTGGGTTGGAGCAAAACTGTGCAGAGCAGCGGCCCTCCAGTAATCGAGTTTGGGACCTACACTATAGAGTGAGAATGACCTGTGGTGATTGAACAGAATCATACCTGTGTGGTTCAAACA[G/T]GAAGAAGAAACGAGCTGTAAAAATGATGATCACCATCGTCCTGCTGTTCACCGTCTGCTGGGCTCCGTTTCATATCGTCCACATGCTCTTTGAGTACAGTAAGTGCAGTTGCTGGACAATATGACCTCAATTAACTGGAAACCTGACATCAGTTTTGATTATTAAACAATTGTGTTGTTTTAAAAATAATTTCCACCCTAATAGTTCATTCAGAGTTTGTAAATACAGTCAAATATTTAAGGTAGGACACCGTTTCCTATTTGAATAGTGGATTTATCTTTGTTAAATTACACAAATTGAAGGACTATATAGGTTTTTTTGTTGAATATTTTACAGAACTGAAATCACAGCACACGTTGCTTGCCACGAACACTTCTTTTGAAAGAATATCTGTTTTATACAAAAAAATTGTAACTATAAAACAACTATAAAATAAGAACTAGCATTTTTTACAAATGAAAATACATTACACTACCCGACAAAAGTCTTGTGGCCTATCC

Associated Phenotype:

Not determined