ZMP

LOC564832

Ensembl ID:

ENSDARG00000075802

Human Orthologue:

GRIN3A

Human Description:

glutamate receptor, ionotropic, N-methyl-D-aspartate 3A [Source:HGNC Symbol;Acc:16767]

Mouse Orthologue:

Grin3a

Mouse Description:

glutamate receptor ionotropic, NMDA3A Gene [Source:MGI Symbol;Acc:MGI:1933206]

Alleles

There are 7 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21642	Nonsense	Available for shipment	Available now
sa10612	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa21642

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109916	Nonsense	149	1114	1	10

Genomic Location (Zv9):

Chromosome 10 (position 4512030)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	4291857
GRCz11	10	4315224

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTATTACTCGCTTCAGAGAGCCTCAATCGAGTGGCGGGGCTTTTACCTTA[C/A]AACCTCACGCTCGAGATTGTCATGGCTGTGGAAGCAGGGCTTGGAGAATT

Long Flanking Sequence:

AGGTGGACGTGGATCCCGTCGTTTCCAGAGATTAACCGAGCCTTGTTTGGAGTAATGCCGGGCTCTTGGATCTGGGGTGCGCTGGGAAGGTTGATGTGGCTTTCATTTCTTGCGCCAAGCGCTTTGATAATGATCCTCGTTCCTCCGGCGTCTCTGGCGCATCCACAACCATGTCAGATTCTGAAGAGAATCGGACATACGGTGAGAGTCGGAGCTCTGCATCTTCAGCCTCGAGTATTCAGGCAGGATTCCTTCAGTGGGAGAGATCTGGACTGGGATGCGGACAGAGAAATGTGGGAAGAGTGGGATGTGATATTTCAAAGTGACCACGAAGAAGACTGGAGGGGTATCAGGACTAAAAGCTCAGTGAATAACCTCAACAAGGCCTCCAAAAGTAAAACCGTACTCAAACAAGTGGCTCCGGATGTTGTGTTTCTGCCACGAGACTCTGTATTACTCGCTTCAGAGAGCCTCAATCGAGTGGCGGGGCTTTTACCTTA[C/A]AACCTCACGCTCGAGATTGTCATGGCTGTGGAAGCAGGGCTTGGAGAATTACCTGCTTTCTCCTTTTCCTCTTCATCTACACCTGCCTGTGCGGATCCTGTGTCGTTCCTGCAAAGTGTTTGCCACACTGTCATTGTTCAAGGAGTTTCTGCCATCATTTCGTTTCCTCAAAACAGGGACGAACTGGTGAAGTTGGAATTTATTGCCTCAACGCTGCAGATTCCAGTCATCAGCGTCGTCCAGAGTGAATTCCAACGACAGACTCAGGTGTGTTGATTTCGAAAATAAATCTTTTTTACACTCTAAACTCTGTAAAATATGCTAAAAAAAATTTATTTTTGTCTAAACGACGGTTCTATATTCATAAGTTTTTGGTTTGTAAACTTGTAACAGTCAAACATTTTTCAACGCCATCTTATTATAGATGTAATTAATATCAAGTAGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa10612

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
Order Allele From EZRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109916	Essential Splice Site	1004	1114	9	10

Genomic Location (Zv9):

Chromosome 10 (position 4543224)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	4260663
GRCz11	10	4284030

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCRACATTCAAAGAAGACAAATTGCAGACAGTTGCAAAACCGGAGAAAAG[G/A]TAAACCRCTTTCATATCAAAATACATTCAGGCAACCCTGAATTAMTGTTC

Long Flanking Sequence:

CAATAGCCTAAATAATAATCAAAGTTCTACGTGAGGGAGGCTAAATACTGACCACATTTTATTCACAATGAACCATCGCTCTCTTCTAAACTCGACTTTCTGTTGTCACTGGCAGACTTTACAGATGGGGATAAAGCACTTCTCAGGGTTATTTGTCATGCTATGCGTTGGAGTGGCCCTGTCTCTCCTCACCACCCTGGGTGAACACATCGTCCATCGCTGGGTGATTCCCAGAATGCAGGAGTCAACAGAGCATAAGTACTGGCTCCACACCAGTCAAGTAAGTTCACTCCTTGCGTTTTATTGCGCATAATTACATGTCATCTCGGCGACACGTTGTAACACTGAGGGAAAACATGCTTTGCTTATTATTCACTTTGCAATTCGCAGTGCTTGGCTTTAATAACGCCTAATTTAATTGTTTTCCAGAGATTACATCGAGCACTTAATCCGACATTCAAAGAAGACAAATTGCAGACAGTTGCAAAACCGGAGAAAAG[G/A]TAAACCACTTTCATATCAAAATACATTCAGGCAACCCTGAATTAATGTTCTGTGCTGTTTTGTTTATAGAAATGACATTTAATTAGTTTGATCTTTTGACATCATCTTGTTTTACAAGAGGAAATTTCCTCTTACAGGATTTAATAGGATTTCAGTTTTTGCACTTTTGTTGGTCTTAAGTTCTACAATTAAATATTTTAATGATATATTCTACAAAGGAATAAACACATCTGACTGAATAGTATGCGAGAAATAGTTGATGATAGGTGGTTGAATTATTATTATTACTAATAATTTAACAGATCAAAGTCAATTATTTTGCTTCTACTGTTACTTAAAGAGCCCCTATTATACATATATATATATATATATATGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACAGTTCTGTCTGGATCTTGAATCTGATTGGCAGATAGCCG

Associated Phenotype:

Not determined