ZMP

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
sa45154	Nonsense	Mutation detected in F1 DNA	Not yet available
sa20110	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa45154

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 > A

Consequence:

Nonsense

Transcripts:

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)

KASP Sequence:

None

Flanking Sequence:

ATCATCTTCTGCGTGCCTTTCCAAGCAACCATCTACTCCCTGGAGGGTTG[G/A]GTTTTCGGGTCCTTCATGTGCAAGGTGGTTCACTTCTTCATCAACCTCAC

Long Flanking Sequence:

TCGAGTCTGATCCTCCTGATATTTACTCTCAGCACGGGCCTAGCTTTCATAAGAGCTTTTAAATCTCATCATGCTGCTGTTCAGATTCCGAAAAGATGGGGCAGATTTGCTATCATAGACTTTTACATCAAATCCTCACGTTTTTTTTTTTCAAAAGAGCAAATCCCTGATTTATTTCTTTTTTATTTTTATATATAGGGCTGTGGAACTTCATATCTTAAAATGTCTGATCACGAGGACCTGAATAAAGCCATGGGACACTGGAATGCCTCAGAGAGCTATCAGCTCAACCCAGCCAGTGTCATCGTGTCAGTGGTCTTCTCGCTCATCTTCCTCTTGGGGACCATCGGGAACAGTCTGGTGCTGGCTGTGCTCCTTAGAAGTGGGCAGGTTGGGTACAACACCACCAATCTGTTCATCCTCAACCTCAGCGTAGCCGATTTCTTCTTCATCATCTTCTGCGTGCCTTTCCAAGCAACCATCTACTCCCTGGAGGGTTG[G/A]GTTTTCGGGTCCTTCATGTGCAAGGTGGTTCACTTCTTCATCAACCTCACCATGTATGCTAGCAGTTTCACACTGGCAGCGGTGTCGGTGGACAGGTGGGTGTTTGCTATAGCCATGTTTATTAACATACTCTTATTTCTTTCATACTCTTAGCGGTTCATTTACTTTTACCTAATAACATGTACAACAGTAAATGCATACATTACATCAGATTAAACATCCTCATTGTTTCAATCAGACCCTCCCCCCTTGACCCTAAATTTCATTTCAATTAAATTCATCTTTTTTTCTTTAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGATTAACATAGAAGTTCTAGTAAATTGAAACTGTGTCAGTCCAGTTCAGTTTAGTTCAGTTCAGTGCGGTTTAATTGATCTTCCAATCATATGAGCCCTAAGCTACTTTAAATAACCAGTTTCCAGCTCATTTTATCTTCGTTTGGAAGAAACCCCCCTCCCCTATTCTCCTCCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20110

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

Transcripts:

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)

KASP Sequence:

None

Flanking Sequence:

AGTACCTCTGGACAGCAGTCGACCCGCTTGATGGGATGTCGGAGTCGAAA[C/T]GAGCAAAGCGCAAGGTCACCAAGATGATCATTATAGTCACGGTGCTCTTT

Long Flanking Sequence:

GCAAGTGTTGTAGTGCTGTCCCATTTCTAAGGGGTAAATTTTGAAGGCCTTCCTCTATACAATCTCTTTTTCAAGGGCCAAGGGGAAGCAGAAGGGGTAGTTCGCTCTCGGTGTGATGGGCCCTTTACAGTGTTAAAAAGCAACGAAAATCTCTGATGGTGATGGTGCATTTCTTCTGTTGCAGATATCTGGCCATTCGTTACCCGTTGCGCTCCAGAGAATTGAGAACGCCGTGTAATGCTGTTGTAGCAATGGTGGTCATCTGGGGCCTGTCGCTGGTTTTCGCTGGGCCTTACCTGAGTTACTACGACCTCATCGATTTCGAGAACAGCAATGTGTGCGTGCCTGGATGGGAAGAGCATAACCGTAAGGTTCTGGACACATGCACCTTTGTTTTTGGCTACGTTATTCCAGTGCTGATCGTGAGCCTGTCCTACACCCGCACCATCAAGTACCTCTGGACAGCAGTCGACCCGCTTGATGGGATGTCGGAGTCGAAA[C/T]GAGCAAAGCGCAAGGTCACCAAGATGATCATTATAGTCACGGTGCTCTTTTGCATCTGCTGGCTGCCGTACCATGTAGTGATTTTGTGCTACCTCTATGGAGACTTTCCCTTCAATCAGACCACCTATGCCTTCAGGCTGCTGTCCCACTGCATGGCCTACGCCAACTCCTGCCTCAACCCCATCGTTTACGCCCTGGTGTCCAAACACTTTCGCAAGGGCTTCAAGAAGGTTTTCAGCTGCATCCTCAGCAAGAAGGGACGGAATAAGGTGCATGTGGTCAATGTGGCCAACACCGTTCCCGGATTCGAAGCGGGATCCACTGAAGTGTCTCAAATGAACGAAGAGAACGCCAGACAGAATGAAAGTGAAATGGTCAATCGCCCACTCGCGCAGCCCCAGGACACCACAATGACTATAACGCTGCCATTTCAGAATCAGCCATGAAAATAAAGTGCACGGCTAATGATGCCTTACAGAAGCCTTATTAAAAGAAAACAC

Associated Phenotype:

Not determined