ZMP

Ensembl ID:

ZFIN ID:

Description:

glutamate receptor, ionotropic, AMPA 4b [Source:RefSeq peptide;Acc:NP_997917]

Human Orthologue:

GRIA4

Human Description:

glutamate receptor, ionotrophic, AMPA 4 [Source:HGNC Symbol;Acc:4574]

Mouse Orthologue:

Gria4

Mouse Description:

glutamate receptor, ionotropic, AMPA4 (alpha 4) Gene [Source:MGI Symbol;Acc:MGI:95811]

Allele Name:

sa3112

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016916	Nonsense	158	904	3	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 20948715)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	21960208
GRCz11	21	21996844

KASP Assay ID:

554-2544.1 (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa13954

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016916	Essential Splice Site	163	904	3	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 20948730)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	21960223
GRCz11	21	21996859

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43634

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
ENSDART00000016916	Essential Splice Site	242	904	5	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 20967103)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	21978596
GRCz11	21	22015232

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa23921

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016916	Essential Splice Site	295	904	6	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 20967718)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	21979211
GRCz11	21	22015847

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa23922

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016916	Nonsense	438	904	10	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 20996511)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	22008004
GRCz11	21	22044640

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa8999

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000016916	Nonsense	612	904	11	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 21000251)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	22011744
GRCz11	21	22048380

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Long Flanking Sequence:

Associated Phenotype:

Allele Name:

sa43635

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
ENSDART00000016916	Essential Splice Site	617	904	11	16

The following transcripts of ENSDARG00000059368 do not overlap with this mutation:

• ENSDART00000139525

Genomic Location (Zv9):

Chromosome 21 (position 21000266)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	22011759
GRCz11	21	22048395

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: