ZMP
GRID1 (2 of 2)
Ensembl ID:
Description:
glutamate receptor, ionotropic, delta 1 [Source:HGNC Symbol;Acc:4575]
Human Orthologue:
GRID1
Human Description:
glutamate receptor, ionotropic, delta 1 [Source:HGNC Symbol;Acc:4575]
Mouse Orthologue:
Grid1
Mouse Description:
glutamate receptor, ionotropic, delta 1 Gene [Source:MGI Symbol;Acc:MGI:95812]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41979 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45454 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15073 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41979
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064839 | Essential Splice Site | 92 | 966 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 13710270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 12565923 |
GRCz11 | 12 | 12604226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTGACATTCTCGAACAAAACCTTAATTGCTACCTTACTATGTCTTGC[A/G]GATATCCGCGGACTGCAGGTGTTTCTAGACCAGACATCAAGACAAGGTTT
Long Flanking Sequence:
AACCCGGTTGTGTGCTGTAGAAGTGTAAAAATTACTTTGTTTGCTCCACATCAGGTCAGGATGTGCGTTTACTACAGGCAATATGACATTATGAGTTGCGCCGATGACTCATTATAATCTCAATATTTCATACCTGATGACCTGATGTGGAGGAGAATACATTAGCATTTAAAGTTTTTGCAGTTTCAGGAAGGTTTTTATACTTACAGATAAACCACAGAAGTTACATAAGATGTTTTGACAAAGGTCTTTGATGCTTTATTAGATTTTGAGCATCTTGTGAGCATTTATTTTCATGGAATATGAGGTAGCTCTCAAATTTAATATATTATATCGAACTCTTTGTCCTGAAGATGAGTTTAAGTTTTGGAGGATTGGGGGTACATGAGGTTAAATAATTAATAAAATAATCTTCATTTTCTGGGTGAACTAAGTCTTGAAACATAACCTATTTTGACATTCTCGAACAAAACCTTAATTGCTACCTTACTATGTCTTGC[A/G]GATATCCGCGGACTGCAGGTGTTTCTAGACCAGACATCAAGACAAGGTTTGGATGTGTCTTTGCAACGAGTGGACAGGAACATTAGCGGCGTGTTTTCCAGTTTGTTTACCTCGATGCGCACAGAGGAGCTGAACCGCTACAGGGACACTCTCAGAAGAGCTATCCTGCTTTTGAGTCCTCGTGGAGCCCAGGTCTTCATCCATCAGGTTTGTGCTGCTATTAATGCATTATTGATTTGGTTGTTAGTCTTGTGACAATTTTGGTTTAGATTGGTTTTACTGGACTCCCAGTTAAGAAATACTCAGGGGGCAGTAGCAGAGCACATTGATCTGTCTTGGATCTGTCTCATTTTATTATGAACATTACACTGCATCAGAAGACTTTAAACATGCATATATGCTGTTAATGTATTGACACATTTCTAGGTTTATTCAGATGTTGTTTTTTTTCTGCAATTTGAGTGCATTTTACCGCTTTTAGACCATTTGTTATGACACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45454
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064839 | Nonsense | 540 | 966 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 13900974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 12756627 |
GRCz11 | 12 | 12794930 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACTCGTTGCATAGTGCTATATGGATTGTCTACGGCGCCTTCGTACAA[C/T]AAGGTACTTCAATAAATTCTCCTCCGACAAGTCCATTCAAAGGCACCTTA
Long Flanking Sequence:
TTTATGGATTGGATTTCTAGGCCTAGTTACTGAAAGAATTTTGAGTTTTTCCTAATACAATACAAAAAAAAAAATTCGTTTTTCCTGGTACAGTCCTGCATATTAGCAAACTTTTTAGTTTCCCCAAATGTAATGAATAAAATAAAGTTTAAATAATTTGTTTGTCTTTACAGAGAGCTGATTTAGCAGTGTCTGCCATAACAATAACACCAGAGCGAGAGAATGTTGTGGACTTCAGCAAGCGCTACATGGATTACTCCGTTGGGATCCTACATCGCAAGCCTGAGGAAAAGATCAACATTTTCTCCTTGTTTGCTCCATTTGATTTGGCCGTGTGGGCCTGTATCGCAGCTGCCATTCCTGTGGTGGGCGTTCTGATCTTCTTGCTGACACGGATGCAGATGCTCCGCTCCCAGAATCCTCCAGGAGCCCATCACGCTTCATCCATGTCTAACTCGTTGCATAGTGCTATATGGATTGTCTACGGCGCCTTCGTACAA[C/T]AAGGTACTTCAATAAATTCTCCTCCGACAAGTCCATTCAAAGGCACCTTAAGAAACGACTTATCAGCTTTGCATGTTTTTAAAAGCAGCCAAGGGATCCGCTGATGATTTGACTCTTAGAAAGGCTTAGAAAGATGACAAGAATTAAGCTGCCTTCTGTTGATACTAGGGTGTCAATACATCATTCCTTCTAAGACACAGATGCAAGCATTGTTTAGCAGCTTAAAATATTTAGCGTTTGTAAATATATATATAAAAGTTAAACTAAAAATTACAATTTATTCACCTCACGTTACTCCAAACCCACAGAGCACAAAAGATGTTTTCCTGAAAGTTTTGCAGTTTATTTGCTCTCCTGCTTTCTAACTTGTGTACAAAGGTGTGCTACCAAGCTTCAAAATTGACAACAAAGCACCATACAAAATATTACTAAGGCAGTTCAGTCACGATTACCCTCTGAGGAGTTTTAAAATGTGAATGGGTCTGACAATGTAAATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15073
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 |
---|---|---|---|---|---|
ENSDART00000064839 | Nonsense | 866 | 966 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 13938743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 12794396 |
GRCz11 | 12 | 12832699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGYCTTATGGACGAGGACATGGCACACAAGCAGATCCCCGCACCATCTAT[C/T]GAGATCTCTGCCCTGGACATCGGCAGCATGCCGYCCAGCCAGCAGCGGGA
Long Flanking Sequence:
AATATTAATATGGTTTAAAAAACAAAAACATAATCAATTGTCTAGAAATGTTAGCATATTTAACATCTTCTGTACATTTTAATGTGCATTGATGAAATGCAGACTGGCTCCAGAAATTACAGTGTCACTTGTCTCACTCAAACATTACTGAACTATACTATATTAAATTCCCACTGGCCAAATTTGATTTCAAGGTGCACATTCTATATATTTTTTTCTTCAAACACTCTTCTACTATCTTAAACTTTCCAATTGGACCTATGTAATGCATTTGCAACACAACCTGCATTAATTGAAGTAAGCGTTGCATGGAGCTTAAAAGCAAAAAAAAAAAAAAAAAAAAAAAGCATCCTGGAAGCAGCAGATCTCAGCCTATCTGTTCCTCCTTTCTTCTCTCACCCTCTCTAGGACAAGGAGGTGAACCTGGAACAGGTGCATCGGCGTTTGAACAGCCTTATGGACGAGGACATGGCACACAAGCAGATCCCCGCACCATCTAT[C/T]GAGATCTCTGCCCTGGACATCGGCAGCATGCCGCCCAGCCAGCAGCGGGAGGCTGTGCGAGACTACCCGGGCACGGGCCTGTCTGTGAGCACCTTCCTCCCGGAGCAAGCTCATGGGGTGGGTCGGACACTGATCCAGGGTCCTGGCAGCACCCTGCCCCTTCCTCTCAGCAGCTCCACCATCCCCTCCATCCAATGCAAACACAGGGCTCCCAACGGGGGCCTGTTCCGACAGAGTCCCGGCAAGACACCCATGCCAATGTCCTACCAATCAGTACCAGGAGGACCCATCCCAGAAGCTATTGAACATAGCACATCCATCTAATGCCATCGTCACCATGGGTTGCCTCATACTTGCTTTTCAAAGAAAGCTGAGGTGCGGTTTGAGCTTGAGAAACTGGAAAACTGTGGCGGTGTAAAAAGAGTTAAAAGGAAAAGAAGAGTAAAAAAAAATACGTAGTGATTTTTATTATGAAATCAAAAAAATAAAAACATGGAAAT
Associated Phenotype:
Not determined