ZMP
gria3b
Ensembl ID:
ZFIN ID:
Description:
glutamate receptor, ionotrophic, AMPA 3 precursor [Source:RefSeq peptide;Acc:NP_938174]
Human Orthologue:
GRIA3
Human Description:
glutamate receptor, ionotrophic, AMPA 3 [Source:HGNC Symbol;Acc:4573]
Mouse Orthologue:
Gria3
Mouse Description:
glutamate receptor, ionotropic, AMPA3 (alpha 3) Gene [Source:MGI Symbol;Acc:MGI:95810]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6340 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35652 | Nonsense | Available for shipment | Available now |
sa42362 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22436 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6340
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043180 | Nonsense | 11 | 883 | 1 | 15 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 13095178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12530951 |
GRCz11 | 14 | 12836965 |
KASP Assay ID:
554-4458.1 (used for ordering genotyping assays)
KASP Sequence:
TTGAGAGAAGCTGAAAAAAANTGACTCAAAGCGCGTTGATTTTTTTATTAT[G/A]GCTTTTCGGCACGTCTCTCGCTGGCTTCCCCAATCAGATAAATATCGGTG
Long Flanking Sequence:
CAGCAACCTTCTCGCTGTGAGGCTATTCTGCCACCCATTGCACCACAGTACTGCCCCGAAATGTATTTTCTTTACCCTAAAATATATTTAGAAATATATTTTATATATCTATATCTTCTATAATGCATGCATTGAATATTAATACCTAATGTAAAGTATTACCTAATCTCGTTCTTTAACGTCAGTCAGATTGATCAATATCGCCTTGCTGGTCCAATTGGAGGAGCGGCTCGCTCTCCCTCTGAATGCGATGCTCTCCGTCGCTTCGACCATCTTCAGCACCAGTCCCACACCCCCACTCTCTCTCCCTCTCTCTGCATCTTTCAGACTGTCTCTCTCTCTCTCCGCACATGCAGAAGAATTGTTCTCCATGAGTCGCAGCGCTTTACTCACGGTTGGATTTCTGCGTTTTTGATTCTCCACAAAGACTTCGTTTGATAAGCCTTGATTTTGAGAGAAGCTGAAAAAAATGACTCAAAGCGCGTTGATTTTTTTATTAT[G/A]GCTTTTCGGCACGTCTCTCGCTGGCTTCCCCAATCAGATAAATATCGGTGAGTCCGCCTGGATATATTTGACTTTTTATCACTAGGCTTTGCATGTCGATGTCTGACTGTTCGCATATTAACGTAGGTAACGTTATAGGAAGACGCTGCATCGCATGCTAAGTAGACAAAATGCGATCTAAGAATCCATTGCAAATCATAAAAGAATTGGTACAAATTATAAAACGCTTACGATTAGGATTCCATTACTCTGCATGCATGTCCGCAATCATTTGCTTTTAATAAACTTAAGAGAAAGTTATATACATATAAATTAAAGCGTCAACCAAAATGGTCACGTATGACTGTTGGAACACGTCCATGAATGTGCTTAAAAGAATTTGACGCGACTGCTGAATTAAGTCAGATTTTAATTTTCATATGTATTAAATATGTGCATCATCTTTGATTCGTGTTGTTTGCTCTTGATAAAGGTGGACTCTTCATGCGTTCCACCGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35652
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 |
---|---|---|---|---|---|
ENSDART00000043180 | Nonsense | 126 | 883 | 3 | 15 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 13035948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12471721 |
GRCz11 | 14 | 12777735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCCACACCTCCTTTGTCACACCCAGTTACCCCATCGACTCAGATGTG[C/T]AGTTTGTCATCCAGATGCGCCCTCCATTGAAGGGTGCTGTCTTAAGTCTT
Long Flanking Sequence:
GCATAATTCTATAGCCAGCTCTTCCTGTTAGCTTATAATTATGTAATTTTGAAAATATGAAAAAAGTTACTAAATGTCTTATTGTTCAAACAAAGCCTCTAACAAGCCCCTGATATACTGGATGTGCAGTAAACTTATTAAAGTATTTTTTATAACAGCCTGTCATTTTAGTACAATAATTTTAGTAAAAGAATTGAGAATCACTTACTTTAACCTTCATGTTCCCACTTCATTAACACCTCAATTATTTTATTTACATTGTCATAATTACAAAATGTGCAATTGCTCCAAGCGTTTTGAGAGAGTAAGCAGCAGTCAACATGGTTTGATTTCGTTGTGTGTCTTGCTTTTCTCTGATTACAGTTTGTTCGCAGTTCTCCAGAGGGGTGTATGCCATCTTTGGCTTTTATGACAAGAAGTCTATGAACACACTGACCTCCTTCTGTGGAGCCCTCCACACCTCCTTTGTCACACCCAGTTACCCCATCGACTCAGATGTG[C/T]AGTTTGTCATCCAGATGCGCCCTCCATTGAAGGGTGCTGTCTTAAGTCTTCTTTCTCACTACAAGTGGGACAAGTTTGTCTACCTCTATGACACAGACAGAGGTAAGTCCTCCAAGCTGTCTATTAAACTCTAGCTGAAATATGAGTGGATGAAATTGTTGATGTGCTGACTTGTATTGTGTTTTTTCAGTTTGTAGCACATACTGGGCAGAATATGATGGAGGATAGATGCCCCATTTGAGTCCTTAGGGTTTGGATAAGTGCCTGAAGTACTGGTGCAAAGGTCCAGATATCTCTGGATACATGATGAATTTAGAACTGATGTGCCCCAGTTTTGTGCAGCGTAGAAAAATTTGGGGCTCTAAAATGTTTCATGTATCAAATAGCTCAACTTTCTTTACTAGTACAATTTATTTGTATTAGGCAATCACAGTGAAATTTATTCTGAGCAGTTTTTAAAAATTTATCTTTTATTACTAATAAGGTAAATATGAAAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42362
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043180 | Nonsense | 249 | 883 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 12912403)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12348176 |
GRCz11 | 14 | 12654190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTTCATAATCTCTTTTCACAGGGCTTCACCAACATTAGCCTGGAC[A/T]AGGTCTTCCTTGGTGGAGCAAACATTAGTGGATTTCAGATAATTAATCCT
Long Flanking Sequence:
TCATGTACATTTGTTAACTGATTGTTTCTTTATTTCAATTGTGTTTATTGTTATTATTATTACTATTAGTTATACTAGTAGTAGTAGTAGTAGTAGTAGTATAAATGTTAATAACTATAGTTTTACATTTATTGTCACATAAACTATGCTTTAGTTCCTCCTTTAATTCAAATGTCACTTCAATTACAATTCTCTATTATGTGTTGATACTTACTGTCAAGTGGGCTACCATATGCATTTCTAAATGCTAATGACAGCAATATATGTAAAGTTTTACTTTAACCCCCGTGTTATCTTAGGATTCTGTATACAACATTTGCCCATAGGGTCAAAAATTACCCCTTCACTAAACCTTTAAAACAAAAATAAAGCAGCTAAATGTAAATTTAATGTGTGTGTGTGTGTGTCTGTCTATGAGTGTGTGTAAATGAAAATACTTATATTTAAAGCTTTTTTTTCATAATCTCTTTTCACAGGGCTTCACCAACATTAGCCTGGAC[A/T]AGGTCTTCCTTGGTGGAGCAAACATTAGTGGATTTCAGATAATTAATCCTGAAAACTTAGTTGTACAGCAGTTTCTCCAAAGATGGGACCGTCTTGATGAAAGAGAATTTCCTGAAGCCAAAAACACACCTCTGAAGGTCTGAAACAACAATTTAAAAAAATCAAATCAACTATAGCATGTCATTGTCACTTATTCCTGTAACATTTCTTTCTTTCTTTCTTTCTTTCTTTTTTTCTGTCTTTCTTTCTTTCTTTCTTTCTTTCTGTCTTTATTTTGTTCTTTCTTTCTTTATTTCTTTCTTCATTAAAACTGGAGATCATTTTACATCTAATTAAACAATAATTATGAGATGAATGAACATATTTTAAAGGGCACCAATTTTATTTCTTTTTCAAAATCTTCAGGTCTTCGGTGTCTCTAGTATGTGTCTGTAAAGTTTCTGTTTAAAATACCCATCATATTATTTATTACTTTTCTATATATGGGAATTTTGAGGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22436
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000043180 | Nonsense | 739 | 883 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 12813098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 12248871 |
GRCz11 | 14 | 12554885 |
KASP Assay ID:
2260-7344.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTTCTTGAATCCACCATGAATGAATACATTGAGCAGAGGAAGCCCTG[C/A]GACACGATGAAAGTGGGCGGCAATCTGGACTCTAAGGGCTATGGTGTGGC
Long Flanking Sequence:
AAAAGCACATTTATAATGTGTTTTATGATTGTACTTTTATACTTTGTTACTGATGAATTTAGTATTGCATTACAAACCATTTGTGTTTAATAGTAGTTTGTGGTTTATAAGATTATTCAGAACGAGTTGATTAATAAACTATTTAAATCAGTTATTATTTAGGCATATAGTAATGGTTACTATGTGTAATACATACTTTATTAACACGTTTATGCAGTTTTGTGACCTAGTCTTTAGGTCTCATATAAAATTGTGTTATTTTTCACTTTCTCTACAATGTAATATAAGGCTGCTTGTGTTTTTTCTCTCCTTGTCTTTCTTTTACAGAGATCAAAAATAGCAGTGTATGAAAAAATGTGGTCATACATGAAATCGGCTGAGCCATCTGTCTTTGCCAAGACCACACCGGACGGCGTGGCACGGGTACGAAAGTCGAAGGGAAAGTTCGCATTTCTTCTTGAATCCACCATGAATGAATACATTGAGCAGAGGAAGCCCTG[C/A]GACACGATGAAAGTGGGCGGCAATCTGGACTCTAAGGGCTATGGTGTGGCGACCCCCAAAGGCTCAGCATTAAGGTGGGTGGAATAATATAACAATATTGTCCATGTTGTTATAGTATTCCACCTACCCTGATGTCCTGTGTTGTCATTTCCTCCCCTCCTCCCCTTCCCAAACCCCCTTTATTAAGAAAAGAGGTAAAGGTATTATGCATTTTGAATGATATTTGATGCTTTCACAATGATGCTTTTGATCAGTTTTTTCTTCTTTAAATGTTTGTCTTCTTTTCCATTTTCTCAAACAGATTTTTATCATTTCGAGACTTAGTCAGTGGTTAATTTAAGCAGTCATTTCACATTTGTGTGTGCGAGTGTGTGCGTGTGTGTGCGCGTGCGTGTATGTGTGTCCCTTCTCGTCTTTTTTGTCCTTCGATCTTTCTCTTGCTGTCTCATGTGGCTGTCCTTCCTGACAGTTGTGTTGTCACTTTTAATTTAACAGTTCAA
Associated Phenotype:
Not determined