Busch Lab

ZMP

gria2a

Ensembl ID:
ENSDARG00000070173
ZFIN ID:
ZDB-GENE-020125-3
Description:
glutamate receptor, ionotropic, AMPA 2a [Source:RefSeq peptide;Acc:NP_571969]
Human Orthologue:
GRIA2
Human Description:
glutamate receptor, ionotropic, AMPA 2 [Source:HGNC Symbol;Acc:4572]
Mouse Orthologue:
Gria2
Mouse Description:
glutamate receptor, ionotropic, AMPA2 (alpha 2) Gene [Source:MGI Symbol;Acc:MGI:95809]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa12891 Nonsense Available for shipment Available now
sa8383 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12891
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077805 None None 250 None 5
ENSDART00000102782 Nonsense 768 875 14 16
ENSDART00000138791 Nonsense 697 804 12 14
Genomic Location (Zv9):
Chromosome 1 (position 20120583)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 20645000
GRCz11 1 21337937
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATCGTTTGTTTAAGAAACGCGGTAAACCTTGCAGTGCTAAAACTGAAY[G/T]AGCAGGGGCTTCTGGWTAAATTGAAAAACAAATGGTGGTAMGACAAAGGA
Long Flanking Sequence:
CCATAAGCATTACAGAATGTCTAAGCTGATGATTCAGAGGCTGAACAGTAACTTGATTATGAATGCATTTGATGATGCACCGTTTGAACTATGCATGCTGTCTTTCTTGATACTTCTAACCAGGTTTGTTTGCTTCAACGCTTAAAATGTTCTCTGCTAACTGATTTGAGGATCTGGATGTGCATTTGAGCAATAACTGATACTATCACTGATCCTCCTCTGTTCTAGCCTCCTGCCTCAAGAGTTTGAGTTTACAAAAAAAGAACTCTTAAAGCTCGACCACCTTACATTTTGATGGGTCGTTGAATACAATTTTGATTGGTTGATTGATTTGACTGACTTACTGATTGATGGATTGTCTAACCCAATGTTCCATTCATTCTATGCGACTTTTGGGGGGCGTGGCCCGCTGCAGCCCCGCCCCCCTCCATGCTGTCTGACAAGTATGTTTTATCGTTTGTTTAAGAAACGCGGTAAACCTTGCAGTGCTAAAACTGAAC[G/T]AGCAGGGGCTTCTGGATAAATTGAAAAACAAATGGTGGTACGACAAAGGAGAGTGCGGCAGCGGAGGCGGGGAGTCAAAGGTCAGACCCGTGCTCGGGATTGTGGGTTCAAAATGAAATGAACAAAATGCAAATGAGCAGGAAGCACTACCAGAGAACCCAGAAAGACAAGCCTAATGCCTACAAAGCTGCTATCAATTGGCCAGTTTGTCGACAACATCTGGTCCAGAATGAAATGCAGACAACCTAAAAAACAGATTCTCAGAGGTATACGGCTCGTTGGCGGGCGCTGTTTCTGCTTCCTGCTCGCGGCGATGAGTCTGTGCACATCTGGCACGGCAAAGCCGCGTTTGCCGACTGCCAAATGGAGCGCAGACTGTCGATCGCCACCACGCTCAGGGCTGAATCATGACCAGCGCTGTTAGCGAGTGCAAATGTTACTGACAATAACATAAAATAACATTGGTAATGTTATTTATGTTATTTCCCATACGCGAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8383
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
ENSDART00000077805 None None 250 None 5
ENSDART00000102782 Nonsense 781 875 14 16
ENSDART00000138791 Nonsense 710 804 12 14
Genomic Location (Zv9):
Chromosome 1 (position 20120542)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 20644959
GRCz11 1 21337896
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACTGAAYGAGCAGGGGCTTCTGGWTAAATTGAAAAACAAATGGTGGTA[C/A]GACAAAGGAGAGTGCGGCAGCGGAGGCGGGGAGTCAAAGGTCAGACCCGT
Long Flanking Sequence:
TGAACAGTAACTTGATTATGAATGCATTTGATGATGCACCGTTTGAACTATGCATGCTGTCTTTCTTGATACTTCTAACCAGGTTTGTTTGCTTCAACGCTTAAAATGTTCTCTGCTAACTGATTTGAGGATCTGGATGTGCATTTGAGCAATAACTGATACTATCACTGATCCTCCTCTGTTCTAGCCTCCTGCCTCAAGAGTTTGAGTTTACAAAAAAAGAACTCTTAAAGCTCGACCACCTTACATTTTGATGGGTCGTTGAATACAATTTTGATTGGTTGATTGATTTGACTGACTTACTGATTGATGGATTGTCTAACCCAATGTTCCATTCATTCTATGCGACTTTTGGGGGGCGTGGCCCGCTGCAGCCCCGCCCCCCTCCATGCTGTCTGACAAGTATGTTTTATCGTTTGTTTAAGAAACGCGGTAAACCTTGCAGTGCTAAAACTGAACGAGCAGGGGCTTCTGGATAAATTGAAAAACAAATGGTGGTA[C/A]GACAAAGGAGAGTGCGGCAGCGGAGGCGGGGAGTCAAAGGTCAGACCCGTGCTCGGGATTGTGGGTTCAAAATGAAATGAACAAAATGCAAATGAGCAGGAAGCACTACCAGAGAACCCAGAAAGACAAGCCTAATGCCTACAAAGCTGCTATCAATTGGCCAGTTTGTCGACAACATCTGGTCCAGAATGAAATGCAGACAACCTAAAAAACAGATTCTCAGAGGTATACGGCTCGTTGGCGGGCGCTGTTTCTGCTTCCTGCTCGCGGCGATGAGTCTGTGCACATCTGGCACGGCAAAGCCGCGTTTGCCGACTGCCAAATGGAGCGCAGACTGTCGATCGCCACCACGCTCAGGGCTGAATCATGACCAGCGCTGTTAGCGAGTGCAAATGTTACTGACAATAACATAAAATAACATTGGTAATGTTATTTATGTTATTTCCCATACGCGAAGAACGCCAGTAAACCTTGCAGTATTGAAACTCAGTGAGCAAGGC
Associated Phenotype:
Not determined