LOC798737

Ensembl ID:
ENSDARG00000044969
Human Orthologues:
GALR2, GALR3
Human Descriptions:
galanin receptor 2 [Source:HGNC Symbol;Acc:4133]
galanin receptor 3 [Source:HGNC Symbol;Acc:4134]
Mouse Orthologue:
Galr2
Mouse Description:
galanin receptor 2 Gene [Source:MGI Symbol;Acc:MGI:1337018]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa45154 Nonsense Mutation detected in F1 DNA During 2018
sa20110 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa45154
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
ENSDART00000066104 Nonsense 93 378 1 2
Genomic Location (Zv9):
Chromosome 3 (position 43147622)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 42761858
GRCz11 3 43467873
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATCATCTTCTGCGTGCCTTTCCAAGCAACCATCTACTCCCTGGAGGGTTG[G/A]GTTTTCGGGTCCTTCATGTGCAAGGTGGTTCACTTCTTCATCAACCTCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20110
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 > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066104 Nonsense 231 378 2 2
Genomic Location (Zv9):
Chromosome 3 (position 43140487)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 42768993
GRCz11 3 43475008
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGTACCTCTGGACAGCAGTCGACCCGCTTGATGGGATGTCGGAGTCGAAA[C/T]GAGCAAAGCGCAAGGTCACCAAGATGATCATTATAGTCACGGTGCTCTTT
Associated Phenotype:
Not determined

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