ghrhr

Ensembl ID:
ENSDARG00000037341
ZFIN ID:
ZDB-GENE-050315-2
Description:
growth hormone releasing hormone receptor [Source:RefSeq peptide;Acc:NP_001124524]
Human Orthologue:
GHRHR
Human Description:
growth hormone releasing hormone receptor [Source:HGNC Symbol;Acc:4266]
Mouse Orthologue:
Ghrhr
Mouse Description:
growth hormone releasing hormone receptor Gene [Source:MGI Symbol;Acc:MGI:95710]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa19901 Nonsense Available for shipment Available now
sa38360 Essential Splice Site Mutation detected in F1 DNA During 2018
sa44550 Nonsense Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa19901
Current 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:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054331 Nonsense 126 432 5 13
Genomic Location (Zv9):
Chromosome 2 (position 52483482)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 51200379
GRCz11 2 50934599
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATTAAGTCTTTTTTGCTCTTTGCATTTATTTTTTCAGACAACCTACTTAT[C/A]GACTTTAAAACAGCTTTACACCGCAGGATACGCAACATCGCTAATATCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38360
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054331 Essential Splice Site 250 432 7 13
Genomic Location (Zv9):
Chromosome 2 (position 52491386)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 51192475
GRCz11 2 50926695
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTCGTCTCGCAGAGGAAATACTTCTGGTGGTACATTCTCATCGGATGGGG[T/A]TCGTAAAACCTGAAAAACAGCACAGAAAAAAAACACAAGCTTCCAGGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44550
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000054331 Nonsense 391 432 13 13
Genomic Location (Zv9):
Chromosome 2 (position 52511594)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 51172267
GRCz11 2 50906487
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TATGGGTTTCTTTCTCTTTCAGGTCCAGGCTGAGCTAAAGCGCAGGTTAT[G/A]GACGTGGCAAACACAAACACACCTGAGCCCGTGTAAAAAGCGTCGTGTCA
Associated Phenotype:
Not determined

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