ZMP
gria4b
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]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13954 | Essential Splice Site | Available for shipment | Available now |
sa23921 | Essential Splice Site | Available for shipment | Available now |
sa23922 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13954
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:
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:
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:
GACCACTATGACTGGAATCGCTTTGTCTTTCTCTAMGACACCGACAGGGG[T/A]AAGACAATTAAACACCMACTCATAATAATGCACAGTTCACTTTGCTGGGT
Long Flanking Sequence:
ACTACGGTGCAGAAATGAGCTGAACTGGTAATCGAATCCATGTAGAAAATATATGCGCTTGTTCAGGTGGTGGATGGGTCTCCCAGGCTGTTTCATTAATGTTTCAAACACCTACGGAAAAGCCCTACACAGGATCACTAACGTAAGCTAGGTCCTAATGCTCTAAAGTGAAGTAAATGTTCAGCGCTCCCTCAGGAATTATGTAATTAATGTTTTAAGCATCTAACTCTCTCTTCCTCTTTGTTGTTGTGCTTTGCAGTCTGTTCCCAGTACTCACGGGGCGTCTTCGCCATTTTCGGCCTGTACGACAAGAGGTCGGTTCACACGCTAACATCATTCTGCGGCGCGCTGCACATCTCCCTCATCACACCCAGTTTCCCCACCGAGGGCGAGAGCCAGTTCGTCTTACAGCTGCGGCCCTCCATACGAGGGGCCCTGCTCAGCCTGCTGGACCACTATGACTGGAATCGCTTTGTCTTTCTCTACGACACCGACAGGGG[T/A]AAGACAATTAAACACCCACTCATAATAATGCACAGTTCACTTTGCTGGGTAGATCAGAGAAATGCCCGTGAAAATGATTAACAGGTATGCATACTGGCTTTGAATATTAAAGGGATAGATCACCCAAAAATTAACATTTCCTGTTAATGTACTCATCCTCAAATCATCCAACATTTAGATGTATTTCTTTCCTTCTTCAGTAGAGCATTGAAGAAGATTTTTTAGCTGAATATGTGGTCCTTGGTTATTTATATAATGGCAGATAAGGACTTAAGTTTTCACTTTAGTGTGAAAACACTCATTGTCCATATGTATTGGCATTTTTACTGTGTTTTAGAAAAATTTTCCCACTATATATACTAAAACTTATGATATGTGACCATTCATGCTCAGTGGGCATGTGCAATGTTTGCCTGCATCAGTTCTTGCCATCTACCAGTTGTGTAATGGTTATATGAGAGTGACATGACGAATCAGGGAATGATATTTAATTCTTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23921
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:
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:
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:
None
Flanking Sequence:
GAACAAGCTGGACCAGCGCGAGTACCCCGGCTCTGACGCACCTCCCAAGG[T/G]AACGTTGCATGGCTTGGTCCAGCGCACAACCGCTTTGAAGCCTGATATAT
Long Flanking Sequence:
TTCCATCTCTTTAGTTGTCTTGTCCTCTCTGTTTCCTGCCCTCCCTCGTTCTTTTTCTTTCTTAATCCTCGCTTTTCTTTAAGCAAGATACGTCAATTTGAGAGACTAATTCGTATTCCAGTGTGAGCGCTGGTGACAGTGTTTTAATGATGCTGGGAGCTGCAGAGCGTGCTCTCTCTCCCTGCTCTCTGGCTGTGCACAGAATTGGCTCAGAGAGGCAAGCTGGATATGAATGTTTGTGGAATTTCTCTTATCATAGCGCTGCATTGCCGACGACGTTTTAATAATCTCTCTCCCTCTCGCTGTATTTCTTACTCTTTCCCCTTCTTTGCTCTGGCAGGGTTTTAAGGACATCAATCTGGAGCGTTTCATGCATGGGGGAGCCAATGTGACAGGCTTTCAGCTGGTGGACTTCAGCAATCCCATGGTTATTAAACTCATGCAGCGCTGGAACAAGCTGGACCAGCGCGAGTACCCCGGCTCTGACGCACCTCCCAAGG[T/G]AACGTTGCATGGCTTGGTCCAGCGCACAACCGCTTTGAAGCCTGATATATTAGCATAAATGCATAAGCGTCCTACTTGAGTCCCTCCAGCCACATTGAGAAAACTTGCAAATTACAACAAGACTGTTGATCACACCCACTGGCTTTATAAATGTGTTTAAACTATGCAGAAAGTATGGATGGAAGTAAGTAAGTAAGTAAGTAAGTAAGTAAGTAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAAGAAAGAAAAAAATGAAAGAATTGAAGAATGGATTGATAAGTGGTTGGGTTAGTTAATGGATGGAAACATAGAAAGCAGTAGAGGATGAGGGGATGAAAGGAATGAAAGAGAAAAATAGATGGAAAAGGGTATATATATATATATAATATATATATATACTGTATGTATATATATATATTAGCGCTGTCAAAATTAACGCGTTAACGCATGCGATTAATTTTAAATAATTAACCCGTTAAAAAAAATTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23922
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 |
---|---|---|---|---|---|
ENSDART00000016916 | Nonsense | 438 | 904 | 10 | 16 |
The following transcripts of ENSDARG00000059368 do not overlap with this mutation:
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:
None
Flanking Sequence:
TCATTTAGGAAGGGCCGTATGTAATGCTGAAGAAAAACTGGGAAATGTAC[G/T]AGGGGAATGAGCAATATGAGGGATACTGTGTGGATTTGGCATCTGAAATT
Long Flanking Sequence:
GACTTTTATGTAAAAAAACTATATTTATTTTCATTGTTTTCTTATGGCTAGCATTTGATAAGCACACGCAAACCTATAATGACTGTAATTATCTTTATATGCCTTATGTGATATTTCAATACTTGTATGAACCCTTTGTTATGGTTTCATAAAGCCTTTGGGATATTTTAAAAGTGTTTGATAATACTTTATTAGGGAATGTGAGGACATATTGACTTATGTTAAAGAAAAAACTATATTTTCATTGTTTCTTTATGGCTAACATTTGATTAGTACATGAGAACATAAAGACTGTAATTTATGTTCATTAAGATCTAAAAAGCAGCTTTGTTCGTCTATACCTTCACAATAAGTCATATTTGAAATGTATAGCAGGTTTACAACCACTTTGAACATGTTTGTTTTGTTTAGAAGTGTGACATGCTGCCCATTGAAAGTGCTCTGTTTTGTTCATTTAGGAAGGGCCGTATGTAATGCTGAAGAAAAACTGGGAAATGTAC[G/T]AGGGGAATGAGCAATATGAGGGATACTGTGTGGATTTGGCATCTGAAATTGCCAAACACATCGGTTTCAAGTATAAGATCTCCATCGTGCCTGATGGAAAGTACGGAGCTCGAGACCCAGAGACTAAGATCTGGAACGGGATGGTCGGGGAGCTGGTGTACGGGGTAAAGCATTTTCCTTTTTTGCAATTGTCTGACATTAGCATTAGATTTATAAATGACATTTGATTGTTTGATGGACATGCTTAATATTGGCTGTTTTGCCATTCATTTCTTGTTTTAATGCTTTCCTAAAATTTTTCCTAAAATCTCCCGTAATTTAAAATGTTTGAGGTCAGTGTGATTGATTGATTGATTGATTAAGATATTTATACGATAATTCAGCAATAATTATTTGTTTTATTTTAACAAAAGTAAAGCCACCTTTCCAATGCACATGACAAACGACAAGCGTTAGACCGGAAGTCATTCATTTCCAATGCAGAGGAGTCCGGGAGCTGC
Associated Phenotype:
Not determined