ZMP
LOC564832
Ensembl ID:
Human Orthologue:
GRIN3A
Human Description:
glutamate receptor, ionotropic, N-methyl-D-aspartate 3A [Source:HGNC Symbol;Acc:16767]
Mouse Orthologue:
Grin3a
Mouse Description:
glutamate receptor ionotropic, NMDA3A Gene [Source:MGI Symbol;Acc:MGI:1933206]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34817 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21642 | Nonsense | Available for shipment | Available now |
sa34818 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30931 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41580 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10612 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34817
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 |
---|---|---|---|---|---|
ENSDART00000109916 | Nonsense | 119 | 1114 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4511938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4291949 |
GRCz11 | 10 | 4315316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCTCAGTGAATAACCTCAACAAGGCCTCCAAAAGTAAAACCGTACTC[A/T]AACAAGTGGCTCCGGATGTTGTGTTTCTGCCACGAGACTCTGTATTACTC
Long Flanking Sequence:
CCTGTTGGAGAGGAGCGCAACTTTGCTGCGTCTAGGAGATTCACCGGTGATCCATCATCTATCCAGCGCTGTGCAGGAGCCACCGGGCGCGCAGGTGGACGTGGATCCCGTCGTTTCCAGAGATTAACCGAGCCTTGTTTGGAGTAATGCCGGGCTCTTGGATCTGGGGTGCGCTGGGAAGGTTGATGTGGCTTTCATTTCTTGCGCCAAGCGCTTTGATAATGATCCTCGTTCCTCCGGCGTCTCTGGCGCATCCACAACCATGTCAGATTCTGAAGAGAATCGGACATACGGTGAGAGTCGGAGCTCTGCATCTTCAGCCTCGAGTATTCAGGCAGGATTCCTTCAGTGGGAGAGATCTGGACTGGGATGCGGACAGAGAAATGTGGGAAGAGTGGGATGTGATATTTCAAAGTGACCACGAAGAAGACTGGAGGGGTATCAGGACTAAAAGCTCAGTGAATAACCTCAACAAGGCCTCCAAAAGTAAAACCGTACTC[A/T]AACAAGTGGCTCCGGATGTTGTGTTTCTGCCACGAGACTCTGTATTACTCGCTTCAGAGAGCCTCAATCGAGTGGCGGGGCTTTTACCTTACAACCTCACGCTCGAGATTGTCATGGCTGTGGAAGCAGGGCTTGGAGAATTACCTGCTTTCTCCTTTTCCTCTTCATCTACACCTGCCTGTGCGGATCCTGTGTCGTTCCTGCAAAGTGTTTGCCACACTGTCATTGTTCAAGGAGTTTCTGCCATCATTTCGTTTCCTCAAAACAGGGACGAACTGGTGAAGTTGGAATTTATTGCCTCAACGCTGCAGATTCCAGTCATCAGCGTCGTCCAGAGTGAATTCCAACGACAGACTCAGGTGTGTTGATTTCGAAAATAAATCTTTTTTACACTCTAAACTCTGTAAAATATGCTAAAAAAAATTTATTTTTGTCTAAACGACGGTTCTATATTCATAAGTTTTTGGTTTGTAAACTTGTAACAGTCAAACATTTTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21642
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 |
---|---|---|---|---|---|
ENSDART00000109916 | Nonsense | 149 | 1114 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4512030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4291857 |
GRCz11 | 10 | 4315224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTACTCGCTTCAGAGAGCCTCAATCGAGTGGCGGGGCTTTTACCTTA[C/A]AACCTCACGCTCGAGATTGTCATGGCTGTGGAAGCAGGGCTTGGAGAATT
Long Flanking Sequence:
AGGTGGACGTGGATCCCGTCGTTTCCAGAGATTAACCGAGCCTTGTTTGGAGTAATGCCGGGCTCTTGGATCTGGGGTGCGCTGGGAAGGTTGATGTGGCTTTCATTTCTTGCGCCAAGCGCTTTGATAATGATCCTCGTTCCTCCGGCGTCTCTGGCGCATCCACAACCATGTCAGATTCTGAAGAGAATCGGACATACGGTGAGAGTCGGAGCTCTGCATCTTCAGCCTCGAGTATTCAGGCAGGATTCCTTCAGTGGGAGAGATCTGGACTGGGATGCGGACAGAGAAATGTGGGAAGAGTGGGATGTGATATTTCAAAGTGACCACGAAGAAGACTGGAGGGGTATCAGGACTAAAAGCTCAGTGAATAACCTCAACAAGGCCTCCAAAAGTAAAACCGTACTCAAACAAGTGGCTCCGGATGTTGTGTTTCTGCCACGAGACTCTGTATTACTCGCTTCAGAGAGCCTCAATCGAGTGGCGGGGCTTTTACCTTA[C/A]AACCTCACGCTCGAGATTGTCATGGCTGTGGAAGCAGGGCTTGGAGAATTACCTGCTTTCTCCTTTTCCTCTTCATCTACACCTGCCTGTGCGGATCCTGTGTCGTTCCTGCAAAGTGTTTGCCACACTGTCATTGTTCAAGGAGTTTCTGCCATCATTTCGTTTCCTCAAAACAGGGACGAACTGGTGAAGTTGGAATTTATTGCCTCAACGCTGCAGATTCCAGTCATCAGCGTCGTCCAGAGTGAATTCCAACGACAGACTCAGGTGTGTTGATTTCGAAAATAAATCTTTTTTACACTCTAAACTCTGTAAAATATGCTAAAAAAAATTTATTTTTGTCTAAACGACGGTTCTATATTCATAAGTTTTTGGTTTGTAAACTTGTAACAGTCAAACATTTTTCAACGCCATCTTATTATAGATGTAATTAATATCAAGTAGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34818
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 |
---|---|---|---|---|---|
ENSDART00000109916 | Nonsense | 394 | 1114 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4527871)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4276016 |
GRCz11 | 10 | 4299383 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCTTGCACACGGGCGTATGGGCGAGCCTTCGCTGGATCACTATGTC[C/T]AGGATGCTTTGGAGCTGGTGGCGCGAGCGGTGGGATCTGCCGCCACTGTC
Long Flanking Sequence:
CTGCAATGATATCCTCGTTTCTTTCTTCCCAACAGAACTTACTTCATTTCCAGATGGCCATGCAAAATCCCCAAACCTCTCAAGCCAATCTCATCTTCTCCCTGCTGTCCATGAATAACTGGTTCGATGTCAGTCTGGTGATGTGTCAACAGATGAACATATCAGACTTTGTTTTCTTGCTCCACAACAACTCCAAATTTCACCTGGGAACCGTCCTAAAGATTTCCACCAACAGCAGCTCCAAAAACGACTTTCACATATTCCTGCAAGCCCAGCTGGAGTCCATCAAGGACTCGACGTCTACCTTAGTGACCTTCGGATGTGACATCAGGGATATTAGGAGAATCTTCACCACTATTGCAAAGTTTGGTTTGATTCTTCCTGATTACCACTGGATTATAGGAGACTCTCAAAATGTGGAGGAATTACGGACCGAGGGGCTCCCCATGGGACTTCTTGCACACGGGCGTATGGGCGAGCCTTCGCTGGATCACTATGTC[C/T]AGGATGCTTTGGAGCTGGTGGCGCGAGCGGTGGGATCTGCCGCCACTGTCTCTCCACAGCTGGCACTGATTCCTGGCACCACAAACTGCCTGGCAAGGCTTGAGGCTAAAAATCTCACATCAGGAACCTTCCTGTCCAGGTAAATTATTTGATTCACTGTTTGATGCTTTGTAAGGTTTGTGTTGTGAAAATGCCATCATTGACAGGTTGTACAAGAGCGAGGCAGAATAATGATGGTGTCTCTAAGGCCCTGTTTACACCTAGTAATAAAATGTGCTTTTGTCAATCTGTTTGTCTAGTAGACAATGCTAAAGGTGTAAATAAGGTTGATATTGTAAAAAAAGAGCCATAGCGCACATTAATACATCTCTGATATCTATATAATAGGCAATGTTGGACAGTAGCGTCGCTACAAGTAGTGACGCTACTAGTTTAACTACATTTCTCAGTAGCTTGGCAGTAGCGTTGCTACTTTCTAAATCACATGGCTTTTCAGTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30931
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109916 | Splice Site, Nonsense | 440 | 1114 | 2 | 10 |
ENSDART00000109916 | Splice Site, Nonsense | 440 | 1114 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4528009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4275878 |
GRCz11 | 10 | 4299245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGGCAAGGCTTGAGGCTAAAAATCTCACATCAGGAACCTTCCTGTCC[A/T]GGTAAATTATTTGATTCACTGTTTGATGCTTTGTAAGGTTTGTGTTGTGA
Long Flanking Sequence:
TGATGTGTCAACAGATGAACATATCAGACTTTGTTTTCTTGCTCCACAACAACTCCAAATTTCACCTGGGAACCGTCCTAAAGATTTCCACCAACAGCAGCTCCAAAAACGACTTTCACATATTCCTGCAAGCCCAGCTGGAGTCCATCAAGGACTCGACGTCTACCTTAGTGACCTTCGGATGTGACATCAGGGATATTAGGAGAATCTTCACCACTATTGCAAAGTTTGGTTTGATTCTTCCTGATTACCACTGGATTATAGGAGACTCTCAAAATGTGGAGGAATTACGGACCGAGGGGCTCCCCATGGGACTTCTTGCACACGGGCGTATGGGCGAGCCTTCGCTGGATCACTATGTCCAGGATGCTTTGGAGCTGGTGGCGCGAGCGGTGGGATCTGCCGCCACTGTCTCTCCACAGCTGGCACTGATTCCTGGCACCACAAACTGCCTGGCAAGGCTTGAGGCTAAAAATCTCACATCAGGAACCTTCCTGTCC[A/T]GGTAAATTATTTGATTCACTGTTTGATGCTTTGTAAGGTTTGTGTTGTGAAAATGCCATCATTGACAGGTTGTACAAGAGCGAGGCAGAATAATGATGGTGTCTCTAAGGCCCTGTTTACACCTAGTAATAAAATGTGCTTTTGTCAATCTGTTTGTCTAGTAGACAATGCTAAAGGTGTAAATAAGGTTGATATTGTAAAAAAAGAGCCATAGCGCACATTAATACATCTCTGATATCTATATAATAGGCAATGTTGGACAGTAGCGTCGCTACAAGTAGTGACGCTACTAGTTTAACTACATTTCTCAGTAGCTTGGCAGTAGCGTTGCTACTTTCTAAATCACATGGCTTTTCAGTAGCGAAGCTATTTTATTAGTCAAGTAGCGCAGTAGCTTCCACACAAGCTACATTTACAGATCGCGGATCAATAAGTGATGTCACCGACATTCACATAGCCGGTGTGTAGCCGGTGATAGTAAATCTATATGATGGCTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41580
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109916 | Splice Site, Nonsense | 440 | 1114 | 2 | 10 |
ENSDART00000109916 | Splice Site, Nonsense | 440 | 1114 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4528009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4275878 |
GRCz11 | 10 | 4299245 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGGCAAGGCTTGAGGCTAAAAATCTCACATCAGGAACCTTCCTGTCC[A/T]GGTAAATTATTTGATTCACTGTTTGATGCTTTGTAAGGTTTGTGTTGTGA
Long Flanking Sequence:
TGATGTGTCAACAGATGAACATATCAGACTTTGTTTTCTTGCTCCACAACAACTCCAAATTTCACCTGGGAACCGTCCTAAAGATTTCCACCAACAGCAGCTCCAAAAACGACTTTCACATATTCCTGCAAGCCCAGCTGGAGTCCATCAAGGACTCGACGTCTACCTTAGTGACCTTCGGATGTGACATCAGGGATATTAGGAGAATCTTCACCACTATTGCAAAGTTTGGTTTGATTCTTCCTGATTACCACTGGATTATAGGAGACTCTCAAAATGTGGAGGAATTACGGACCGAGGGGCTCCCCATGGGACTTCTTGCACACGGGCGTATGGGCGAGCCTTCGCTGGATCACTATGTCCAGGATGCTTTGGAGCTGGTGGCGCGAGCGGTGGGATCTGCCGCCACTGTCTCTCCACAGCTGGCACTGATTCCTGGCACCACAAACTGCCTGGCAAGGCTTGAGGCTAAAAATCTCACATCAGGAACCTTCCTGTCC[A/T]GGTAAATTATTTGATTCACTGTTTGATGCTTTGTAAGGTTTGTGTTGTGAAAATGCCATCATTGACAGGTTGTACAAGAGCGAGGCAGAATAATGATGGTGTCTCTAAGGCCCTGTTTACACCTAGTAATAAAATGTGCTTTTGTCAATCTGTTTGTCTAGTAGACAATGCTAAAGGTGTAAATAAGGTTGATATTGTAAAAAAAGAGCCATAGCGCACATTAATACATCTCTGATATCTATATAATAGGCAATGTTGGACAGTAGCGTCGCTACAAGTAGTGACGCTACTAGTTTAACTACATTTCTCAGTAGCTTGGCAGTAGCGTTGCTACTTTCTAAATCACATGGCTTTTCAGTAGCGAAGCTATTTTATTAGTCAAGTAGCGCAGTAGCTTCCACACAAGCTACATTTACAGATCGCGGATCAATAAGTGATGTCACCGACATTCACATAGCCGGTGTGTAGCCGGTGATAGTAAATCTATATGATGGCTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10612
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109916 | Essential Splice Site | 1004 | 1114 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 10 (position 4543224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 4260663 |
GRCz11 | 10 | 4284030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCRACATTCAAAGAAGACAAATTGCAGACAGTTGCAAAACCGGAGAAAAG[G/A]TAAACCRCTTTCATATCAAAATACATTCAGGCAACCCTGAATTAMTGTTC
Long Flanking Sequence:
CAATAGCCTAAATAATAATCAAAGTTCTACGTGAGGGAGGCTAAATACTGACCACATTTTATTCACAATGAACCATCGCTCTCTTCTAAACTCGACTTTCTGTTGTCACTGGCAGACTTTACAGATGGGGATAAAGCACTTCTCAGGGTTATTTGTCATGCTATGCGTTGGAGTGGCCCTGTCTCTCCTCACCACCCTGGGTGAACACATCGTCCATCGCTGGGTGATTCCCAGAATGCAGGAGTCAACAGAGCATAAGTACTGGCTCCACACCAGTCAAGTAAGTTCACTCCTTGCGTTTTATTGCGCATAATTACATGTCATCTCGGCGACACGTTGTAACACTGAGGGAAAACATGCTTTGCTTATTATTCACTTTGCAATTCGCAGTGCTTGGCTTTAATAACGCCTAATTTAATTGTTTTCCAGAGATTACATCGAGCACTTAATCCGACATTCAAAGAAGACAAATTGCAGACAGTTGCAAAACCGGAGAAAAG[G/A]TAAACCACTTTCATATCAAAATACATTCAGGCAACCCTGAATTAATGTTCTGTGCTGTTTTGTTTATAGAAATGACATTTAATTAGTTTGATCTTTTGACATCATCTTGTTTTACAAGAGGAAATTTCCTCTTACAGGATTTAATAGGATTTCAGTTTTTGCACTTTTGTTGGTCTTAAGTTCTACAATTAAATATTTTAATGATATATTCTACAAAGGAATAAACACATCTGACTGAATAGTATGCGAGAAATAGTTGATGATAGGTGGTTGAATTATTATTATTACTAATAATTTAACAGATCAAAGTCAATTATTTTGCTTCTACTGTTACTTAAAGAGCCCCTATTATACATATATATATATATATATATGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACAGTTCTGTCTGGATCTTGAATCTGATTGGCAGATAGCCG
Associated Phenotype:
Not determined