ZMP
gria2b
Ensembl ID:
ZFIN ID:
Description:
glutamate receptor, ionotropic, AMPA 2b [Source:RefSeq peptide;Acc:NP_571970]
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 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22520 | Nonsense | Available for shipment | Available now |
sa1498 | Splice Site, Nonsense | Available for shipment | Available now |
sa10318 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22520
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064617 | Nonsense | 250 | 879 | 6 | 16 |
ENSDART00000074671 | Nonsense | 250 | 897 | 6 | 16 |
The following transcripts of ENSDARG00000052765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 37016425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35455752 |
GRCz11 | 14 | 35796066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATTTCATGTTTTTAGGGTTTTGTGGATGGAGATCTTTCTAAAATC[C/T]AGTATGGTGGAGCGAATGTGTCAGGCTTTCAGATTGTGGATTTTGATGAC
Long Flanking Sequence:
GGAGTCAAATCGAAACCGCTATATCTGTCTAAAAAAAAAAAAAAATAAAAAAAAAAAATAATAATAATAATTCACAATCAGATATTTTCCCCAAATCATCAAGCCCTACTTTGGATGTTTATTTGCAACTATGAGAAATAAAAATACAATTCCAAGAAGAAAAGTCCCAATTGTGAGACTCATGATTGCATGAAAAAACTGTATTCTGAGGTTATTCAAAATCCAAAAAAAAACTAAAAAAAACTTTAAATATTAGCTTTTAGTATTTCTAGTGTGTTTATTTTGTAATGCATTGATTAAATGAGATCTTTTATTCTCTTCCCAGGTCATTACTATTGGCAGGCATGTGAAGGGATATCACTACATCATAGCAAACCTGGTAAACTCAAATACAGCACTAACAACAAAAAAAAAAACATCACATTTTTAAAATAGTAGCAATCAAAACAAAAGCCATTTCATGTTTTTAGGGTTTTGTGGATGGAGATCTTTCTAAAATC[C/T]AGTATGGTGGAGCGAATGTGTCAGGCTTTCAGATTGTGGATTTTGATGACCCTCTGGTGTCCAAATTTGACCAGCGCTGGGAAGCTCTGGAGGAAAAAGAATATCCTGGAGCAGACAGCAAGATACGGGTGAGACCTCTGTCTGTGTGTGTGTGTGTGTCCATTTCAGACATCTTTCCTAAGTATGATTAAAAGAGATGTTCAGGTAATTGCTACATGAATGTATAACCTCTTCATTTAAAAGCCCGTATACTTCAGGCCATTTGCAGGAAAAGCTTGTTAGTTATTTTCTACTCCAGATTAAATGTGGTCTCATCTGTCTCGAAGACTAAGCAGGTGCTTCATTTCTGCAGACTGAAATCAAATGTTTCATTTTTTAAATTAGCAAATAAGTCCTGTATAAGTGACATTTAAAACTGAGAATTCCCTTTAAATTCTTTCCTAAATTTGATTTGAATGTAGAATATGATTTATGTTAGTAAAATTCAAATGTATCGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1498
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064617 | Splice Site, Nonsense | 489 | 879 | 11 | 16 |
ENSDART00000074671 | Splice Site, Nonsense | 489 | 897 | 11 | 16 |
The following transcripts of ENSDARG00000052765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 37020387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35459714 |
GRCz11 | 14 | 35800028 |
KASP Assay ID:
554-1423.1 (used for ordering genotyping assays)
KASP Sequence:
GTTAAAAATATAATTTAAGAATTAAACCGAAATTAAATCTCTCGTTTCAG[A/T]AAGCTGACATCGCAGTGGCTCCACTGACTATCACTTTAGTCCGAGAAGAA
Long Flanking Sequence:
GTCACAAAATCAGATCTCTTCCCAAATGACACAATGGGGCTTGAAAACAAGACTGTGATCGTCACCACCATTCTAGTAGGTTTTACTTGTGGTCGTCCAACATATTATTAAGTATTTTTTAGTAAAGCACTACTCTCTGACAAGGTGTTTCCTGGTGTCTTTTTCAGGAAGCCCCATATGTAATGTTAAAGAAGAATGCTGACCTTTTTATGGATAATGAAAGATATGAGGGGTATTGTGTGGACCTGGCAGCTGAAATAGCAAAGCACTGTGGATTTAAATATCAGCTGAAAATAGTAGGCGATGGCAAATATGGAGCTAGAGATGCAGAGACGAAGATCTGGAATGGAATGGTTGGAGAATTGGTTTATGGGGTAAGAAAGATTTTTTAGATGTGATTGAAAATGAGTCGAAAAAATAGCTTCAAGCACTAAGCTCAAGGATATATTGGTTAAAAATATAATTTAAGAATTAAACCGAAATTAAATCTCTCGTTTCAG[A/T]AAGCTGACATCGCAGTGGCTCCACTGACTATCACTTTAGTCCGAGAAGAAGTTATCGACTTCTCAAAGCCGTTCATGAGTTTGGGCATCTCCATCATGATCAAGAAGCCTCAGAAGTCCAAGCCTGGTGTTTTCTCATTCCTGGATCCACTGGCTTATGAGATCTGGATGTGTATTGTGTTCGCTTACATCGGTGTAAGTGTGGTGCTTTTCCTGGTCAGTCGTTTCAGTCCATATGAGTGGCACACAGAGGAATATGAGGATGGACAGATCCAGACCAACGAGTCGACCAATGAGTTTGGGATCTTCAACAGTCTTTGGTTCTCTCTTGGAGCTTTTATGAGACAAGGATGTGATATTTCACCCAGGTTTGTTTGTGATCTTGATTTCTTCAAGAAATGTTGAATTTGTAAAAGTTTTGAATGATTTCGTATGTAAAACAAAGGTTAGATTTGCAGTCATTTCATCATTAGATTGCTAAGGGTAACCTTAGATAAAGTT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa10318
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064617 | Nonsense | 838 | 879 | 15 | 16 |
ENSDART00000074671 | Nonsense | 838 | 897 | 15 | 16 |
The following transcripts of ENSDARG00000052765 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 37030569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35469896 |
GRCz11 | 14 | 35810210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTGGCCATGCTGGTGGCCCTGGTCGAGTTCTGTTACAAGTCCCGAGCC[G/T]AGGCCAAGCGCATGAAGGTGGCAAAGAATGCACAGAATATTAATCCCACT
Long Flanking Sequence:
ATTAACCCCTGCTATAAATGTGAATTCAACAAAGAGAATATTTACTACAGCCATTAGCACGAGGAAATGTAAGAAGTGTGATTTAAAAGCGCTTTGTTGCTTTGGTAGCCATCTCTCAAGAGAATGTTAAAGGCTTTAGTAAATCCATCCCATTCGAGCAGAATTGCTCAATGCCCCCCCATTGCATTGCTTCAAGGGCACATTAACCAGCAGCTGCAGCAGCACAGTTATTGTTTAAACATTACTGTCCTGAGCTGTGCATTTGTATCCACATAGACGTAAAATTGCCACTTAAATATTCTGTTATTTCTACATTTGAATGTTTAATACTGAGATGGTGTGCTTTCCCCGAGCGCTGACCCGTGTCTCGTGTGCATTTTCAGGAGAAGACCAGCGCGCTCAGCCTGAGCAATGTGGCTGGCGTCTTCTACATCCTTGTGGGCGGCCTGGGCTTGGCCATGCTGGTGGCCCTGGTCGAGTTCTGTTACAAGTCCCGAGCC[G/T]AGGCCAAGCGCATGAAGGTGGCAAAGAATGCACAGAATATTAATCCCACTTCCTCGCAGAATTCACAGAATTTTGCCACTTATAAGGAAGGGTACAACGTATATGGGATCGAAAGTGTAAAAATTTAAGGGGGTAGGATACGCGGCCGTCATTTCAGTCTGTCCCGTGCACGCTTCTTTTGGCTTCCCATCTGTTCCATTCCCTGAATGTTCTAGTGAATGAGGAGATTTGGACCGTAAACTGGATCGTATGTACTGGTGTTCTTATAGTGATAAAAAAGAAAAAAAAACTTCCTTTCTCCGCCTCTGCTGCACATATATACAGGAGAAAAGTTTTTTTTTTGTATACCAAGTGACTTTGTTCGTCCACCTCATTGTCATGTATGACTGTTGTTATATCCTACATCACTATGGGAAGCTTAAATCCGCCATCGAATTTAAAAAAAGATTTCAGTGCGACTGTATCTCACAAATAATACTTTTTTTCACCTACAATATATA
Associated Phenotype:
Not determined