ZMP

grina

Ensembl ID:

ENSDARG00000052746

ZFIN IDs:

ZDB-GENE-040426-1367, ZDB-GENE-040426-1367

Description:

glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1 (glutamate binding) [Sour

Human Orthologue:

GRINA

Human Description:

glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1 (glutamate binding) [Sourc

Mouse Orthologue:

Grina

Mouse Description:

glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1 (glutamate binding) Gene [

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa28759	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa36273	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa28759

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074653	Essential Splice Site	93	337	2	7
ENSDART00000074655	Essential Splice Site	93	328	2	9
ENSDART00000074653	Essential Splice Site	93	337	2	7
ENSDART00000074655	Essential Splice Site	93	328	2	9

Genomic Location (Zv9):

Chromosome 16 (position 57026270)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	53608835
GRCz11	16	53495662

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGCCGCTCCATACAGCACAGATCCATACTCACAGCCGTTTCCCAACGG[T/C]AAGAGTACTGCTTCACACAGGTGGGCCTGACAAACCACCTGTAGACACAC

Long Flanking Sequence:

GAAAACCAACAACAATCAAAAATGCATGATTATATGCTGTCATGGCATTGCAATCAAAATGTGATTATAATGGAAGTCAATGGGGCAAAAATAGACACCAACTTAACCAAAAGAGGGTCAATTTAAACAACACACAGGAAATATAATTGTCCTCTGCTAAGTTGCTTTCATGTAACTCAAAGTGCTTCATATGTTCAGCTGTGTTTTCAGTCTGCTCCAGTGATGTCTCAGAATAAGGGATACAGCCGTTTTGACAATGCTGTGGATGGGGATGATCCTTCACCGCCACCACCGCCGGGTTTCGTGATGCCTCCTGCTTATGAAGCCGCTGTTCAGTACGGGCATGCAGATGCTACAGTCCCCGTGGCTGTTCCAGTCGGACCACCGTACGCTTTTGAAAGTCCTGCGTACGGACAGGGAGTATCCGGATACCCACAGCAGCCGTATCCAGTGGCCGCTCCATACAGCACAGATCCATACTCACAGCCGTTTCCCAACGG[T/G]AAGAGTACTGCTTCACACAGGTGGGCCTGACAAACCACCTGTAGACACACTCTGCTATCTCACTTCTATTCTAGCACCTAATTCTCTGAGCACTAATAATTCCTCTGTATAATCAGCTCTTATTGTGTGTATTGCCAATCGCTGAATGCCTTGTAAGTCACATTGGATTACGTTTAGAAGATAAAAAACTGATGTAAACATCTAAAACTTACAGTTTGTCACCTAAATGCAGGGTTCTTACGGATGCTGGAAATTCTGGACAATGCTTGATTTATAACATAGTGTTTTCACAGTTAGAAAAGTGCTTGGATTTTGGACCGAGTGCTTGAACCTGCTCGAATTTGAAATTGCAGGGCTCAAAATTGCGACCGTTTTGGTTGCATATGCAACTGTGACTTAATCTGTGCGCTGAAAATATATTTGGGAGCATTTCTGTGATTGCATAAATACTTGTTATGCGACCAGTTTTCATTGCAAAATGTTCACCGTATGTATATTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36273

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074653	Essential Splice Site	93	337	2	7
ENSDART00000074655	Essential Splice Site	93	328	2	9
ENSDART00000074653	Essential Splice Site	93	337	2	7
ENSDART00000074655	Essential Splice Site	93	328	2	9

Genomic Location (Zv9):

Chromosome 16 (position 57026270)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	53608835
GRCz11	16	53495662

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGCCGCTCCATACAGCACAGATCCATACTCACAGCCGTTTCCCAACGG[T/C]AAGAGTACTGCTTCACACAGGTGGGCCTGACAAACCACCTGTAGACACAC

Long Flanking Sequence:

GAAAACCAACAACAATCAAAAATGCATGATTATATGCTGTCATGGCATTGCAATCAAAATGTGATTATAATGGAAGTCAATGGGGCAAAAATAGACACCAACTTAACCAAAAGAGGGTCAATTTAAACAACACACAGGAAATATAATTGTCCTCTGCTAAGTTGCTTTCATGTAACTCAAAGTGCTTCATATGTTCAGCTGTGTTTTCAGTCTGCTCCAGTGATGTCTCAGAATAAGGGATACAGCCGTTTTGACAATGCTGTGGATGGGGATGATCCTTCACCGCCACCACCGCCGGGTTTCGTGATGCCTCCTGCTTATGAAGCCGCTGTTCAGTACGGGCATGCAGATGCTACAGTCCCCGTGGCTGTTCCAGTCGGACCACCGTACGCTTTTGAAAGTCCTGCGTACGGACAGGGAGTATCCGGATACCCACAGCAGCCGTATCCAGTGGCCGCTCCATACAGCACAGATCCATACTCACAGCCGTTTCCCAACGG[T/C]AAGAGTACTGCTTCACACAGGTGGGCCTGACAAACCACCTGTAGACACACTCTGCTATCTCACTTCTATTCTAGCACCTAATTCTCTGAGCACTAATAATTCCTCTGTATAATCAGCTCTTATTGTGTGTATTGCCAATCGCTGAATGCCTTGTAAGTCACATTGGATTACGTTTAGAAGATAAAAAACTGATGTAAACATCTAAAACTTACAGTTTGTCACCTAAATGCAGGGTTCTTACGGATGCTGGAAATTCTGGACAATGCTTGATTTATAACATAGTGTTTTCACAGTTAGAAAAGTGCTTGGATTTTGGACCGAGTGCTTGAACCTGCTCGAATTTGAAATTGCAGGGCTCAAAATTGCGACCGTTTTGGTTGCATATGCAACTGTGACTTAATCTGTGCGCTGAAAATATATTTGGGAGCATTTCTGTGATTGCATAAATACTTGTTATGCGACCAGTTTTCATTGCAAAATGTTCACCGTATGTATATTTA

Associated Phenotype:

Not determined