ZMP

NP_001161371.1

Ensembl ID:

ENSDARG00000075012

Description:

glycine receptor alpha 2 [Source:RefSeq peptide;Acc:NP_001161371]

Human Orthologue:

GLRA2

Human Description:

glycine receptor, alpha 2 [Source:HGNC Symbol;Acc:4327]

Mouse Orthologue:

Glra2

Mouse Description:

glycine receptor, alpha 2 subunit Gene [Source:MGI Symbol;Acc:MGI:95748]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21617	Nonsense	Available for shipment	Available now
sa7286	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21617

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
ENSDART00000066192	Nonsense	39	427	2	10
ENSDART00000105620	Nonsense	39	384	2	8

Genomic Location (Zv9):

Chromosome 9 (position 56947384)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	55355108
GRCz11	9	54920229

KASP Assay ID:

2260-2638.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCAGGACTACAGGGTGAACATTTTCCTCCGGCAGAAGTGGAACGACCCT[C/T]GACTGGCCTACAGCGAGTATCCGGACTCGTCTCTGGATCTGGACCCGTCC

Long Flanking Sequence:

TTGCTCTTCAGTGTTTGGACTCTCAGTAATGATTTCAAACCACACTGAACTGAGCTAAACTGAACTGAACTTAAACACTAAAAACTGAATTACCCTGATCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTTTAAAAGCGCTGGTAACACTTTATAATAACTAATGAACCAATGATCCAAAACACAGCCAAGGAGACTCTTGGATTCTTTCAGAGAAAGACAATCAAGCTGTAGAATGGCCCAGCCAGTTACCTGACCCGAATCTAATAGAGAATACAGAATAAAGCTCAGATTTGACAGACGAGACCCACAGAATCATCAAGATATTGACACTCTGTTGAAGTCTGAGAAACTCACACTTGAGCAATGCATGAGGCTTCATTCTCCATATGAGAGGCAATAAATGGAGTAAATAGAGTAAACGCATCTATCTTTCAGGACTACAGGGTGAACATTTTCCTCCGGCAGAAGTGGAACGACCCT[C/T]GACTGGCCTACAGCGAGTATCCGGACTCGTCTCTGGATCTGGACCCGTCCATGCTGGACTCCATCTGGAAGCCTGACCTGTTCTTCGCCAACGAGAAAGGAGCAAATTTTCACGACGTCACGACAGACAACAAACTCCTGAGGATCTTCAAGGACGGAACCGTTCTGTACAGCATCAGGTATGACCGTTTGTTCATGAAGGATCTTACACTGGGTTTACATTAAACACATTGAGAATGCCTGCACTGCTTCACTAGCTCTCCATTACTCAGGGGATGTTTTGCAAAAGGCACAGCTAAAGTAGTTCCGGCAGGTTTGAGCGCATTACAGCTTCATATCACTCCGCTGAATGATTAGAGATATTTCACAGCGACAACAGTCAGAAATCAAATCAGAACACAACAGAAGGAGGAGGAAGAGAAGTGGAGGACACTAGAGATGCACACAGGAGACGCTTGAGGAGGACACACAAGCACAATAGTGCACTCCAGGCTGCTGAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7286

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000066192	Essential Splice Site	422	427	9	10
ENSDART00000105620	None	382	384	8	8

Genomic Location (Zv9):

Chromosome 9 (position 56926741)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	55334465
GRCz11	9	54940872

KASP Assay ID:

554-4472.1 (used for ordering genotyping assays)

KASP Sequence:

AAYGTTTTTTACTGGATCACGTATAAGATCATCAGACACGAGAGCGCAAG[G/A]AAAGACTAGAGATTACRTCATTTATYTGCTGACTTTCACCTGGATTAKTT

Long Flanking Sequence:

GTCAGAATCATGAAACGTTAAACTCAGAATTACTACATTAAAATGTGAATTGTGAAACGTTAAACTCACAATTGCTAAAGATAAAAAATTTAGAATTGTGTGATTGCTAATAACTTTGCAATTTGCTAAATAAAAATGTTTCATTAAAATCCTTTCAATTCAGAGCTTAAATGTGTATTGTATCCTAAAACTGTAAGATTGTAAACTTTCGCCGTCTTCATTTGTGTTGACACACAGGAGGATTTACAGGACGGACGTTTGCATTTTTCCAGCTACAACACAACGACCTGTGTAAAAGATGGCGCCGTGGTCAAAAACACACAGGTGAACCAAATCCAGCAGCCGTCCATCCTGAAAAACACAGAAACAAACCGAAAGAAGTTTGTGGATCGAGCCAAACGAATCGACACCATATCACGCGCCGCATTCCCACTGGCGTTCTTAATCTTCAATGTTTTTTACTGGATCACGTATAAGATCATCAGACACGAGAGCGCAAG[G/A]AAAGACTAGAGATTACATCATTTATCTGCTGACTTTCACCTGGATTATTTTCAGTCAGGGATAAACTGCGCACACTGTGGACGGAAACGGCATCGGCTCGATTTAACGTGGCTGTATTTTAATATTTGATGGTGTAGCTATTTTTTGTGAAAGGTTTCATATGAAAGATGCTGTTTTTTTTACGATTGTCTTTCGAAACTTGATTGTTTTTATTGAATGGAGTAGATTTTCTTCTCTTTATAGACACAACAGCACATTTTACAGCACAAACACACTGAATGGATTATATTGTAGATCTATACTAGTGAATCTCACCAAACTCTGTTACATTTCACCTACAAATCAAATCAAGTGTTATATTATTTGACCAATGTAATATGTTAAATAAAGTTGGTATATATAATTGAAATGTATTATTTGTATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACA

Associated Phenotype:

Not determined