grin2db

Ensembl ID:

ENSDARG00000070620

ZFIN ID:

ZDB-GENE-100920-7

Human Orthologue:

GRIN2D

Human Description:

glutamate receptor, ionotropic, N-methyl D-aspartate 2D [Source:HGNC Symbol;Acc:4588]

Mouse Orthologue:

Grin2d

Mouse Description:

glutamate receptor, ionotropic, NMDA2D (epsilon 4) Gene [Source:MGI Symbol;Acc:MGI:95823]

Alleles

There are 5 alleles of this gene:

Mutation Details

Allele Name:

sa25008

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 2015.

Mutation:

C > T

Consequence:

Nonsense

Genomic Location:

Chromosome 16 (position 15055693)

KASP Assay ID:

None (used for ordering genotyping assays from LGC Genomics)

KASP Sequence:

None

Flanking Sequence:

GCCTCCCCATTGTTGCTGTGGGAGGGGGAGCAGCTCTGGGCAGGGTACCA[C/T]AGGTAATGCCGTTTACTGAATTGAAATGTGGTCATGTTTTTGTTGCTCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15765

Current Status:

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

Availability:

Mutation:

T > A

Consequence:

Nonsense

Genomic Location:

Chromosome 16 (position 15048749)

KASP Assay ID:

None (used for ordering genotyping assays from LGC Genomics)

KASP Sequence:

TCTTCCACCGCACTCCAATTGGAGGTGATCTTTGAGGWACTGGAGGAGTA[T/A]GATTGGACGGCCTTCTCGGTGGTGTCCACCCGTCACCATGGCTACCAGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9877

Current Status:

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

Availability:

Mutation:

C > A

Consequence:

Nonsense

Genomic Location:

Chromosome 16 (position 14952536)

KASP Assay ID:

None (used for ordering genotyping assays from LGC Genomics)

KASP Sequence:

AAAAACATCCGCAGTAACTATCCAGACATGCACCAATACATGGTCAAGTA[C/A]AACCAGAAGAGTGTGGAGGACGCCATCTCYCACCTCAAGACTGGGTCTGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa19134

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 2015.

Mutation:

A > T

Consequence:

Nonsense

Genomic Location:

Chromosome 16 (position 14946227)

KASP Assay ID:

None (used for ordering genotyping assays from LGC Genomics)

KASP Sequence:

None

Flanking Sequence:

ACATGGCTCGTAAAGATGAAGGCTGTAAAGTAATGACCATCGGCTCAGGG[A/T]AAGTATTCGCCACGACTGGATATGGGATCGCCCTGATCAAGAACTCTCGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22781

Current Status:

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

Availability:

Mutation:

C > T

Consequence:

Nonsense

Genomic Location:

Chromosome 16 (position 14933224)

KASP Assay ID:

None (used for ordering genotyping assays from LGC Genomics)

KASP Sequence:

None

Flanking Sequence:

GCTACTATGGACCTATTGATCCAGAGGGACTTGGGCCATGTGTGGACCAA[C/T]AGACAGGTTCTCAAACCCCTAAAACAATCCCCAGAGTCCATCAACAACCC

Associated Phenotype:

Not determined

OMIM

OMIM information for GRIN2D

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