ZMP
narg2
Ensembl ID:
ZFIN ID:
Human Orthologue:
NARG2
Human Description:
NMDA receptor regulated 2 [Source:HGNC Symbol;Acc:29885]
Mouse Orthologue:
Narg2
Mouse Description:
NMDA receptor-regulated gene 2 Gene [Source:MGI Symbol;Acc:MGI:2135947]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38122 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38123 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24715 | Nonsense | Available for shipment | Available now |
sa38124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25236
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121498 | Nonsense | 81 | 929 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 35020982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 33488745 |
GRCz11 | 25 | 33974172 |
KASP Assay ID:
554-7726.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAGTTTCAGATGTTAGTAACGCCTTGGCTGCAGACGAGCCCACGGCT[G/T]AATGCAAACCAACTCAAAAAGCCAAATCTACACCTGAGAAGAACTCTGTT
Long Flanking Sequence:
AAAATTGAGTTGTTGATATTCTTATTTAATGACAACTTATTTACATTATGGAATGTTTTTTATAAGTTGTGTACATTAAGACTTTTTATTAAAGAAAAAACAAATGGCACACACATATTATTTGCTATATGGAATGCAAAAACTTTGAAGGTCATTACCTCAAAATCATTCAGAACTCAGATAGAATCTTATAACTCCATGGTGACGATATGTTAAATATGGATGAATCATAAATAGGAACATAATTTCTTCCATAAATATCCAATGCCATCAAAGTCACTGGGTTTCATTCTACTTTATCTGAATACAAAAATGAAAAGTTGAAATGCAAAACTATTAAATATTATTGAGCTGTATTTTTTTCTTTGTTTTTTTTGTAAAGCTCTGGTGTAAAACCAGAGGACGCTGGTCAGAAAGAGGCCGATGCAGGATCACAGCCAGCGAAGTGTGACGAAGTTTCAGATGTTAGTAACGCCTTGGCTGCAGACGAGCCCACGGCT[G/T]AATGCAAACCAACTCAAAAAGCCAAATCTACACCTGAGAAGAACTCTGTTGTTTCAGCTTTTCCTGAACCCTTAGTCCCGTACCCCTGCTTCACCAAGATCAATGCAAAAGAACGCAGATCATACATCAGCATGCTCAAATCCAAGAATTATAAGAAAGCTTCAAAGGTAAACGCTCAACTTTTAGGGGTGATAATCAGCTTTGCAGACACACAGTGTGGTTTTAATGTATTATAGTTATACACTCACTGGCCACTTTATTAGGTACACCTTACTAGTACTGGGTTGGACCCCTTTTTTCCTTCAGAACTGCCTTAATCCTGACATAATAGCGTCTCCCAGTTGCTGCAGATTTGTCGGCTGCACATCCATGAGGCCAATCTCCCGTTAATATAAAATATGCTCTATTGGATTGAGATCCGGTGACTGTTGAGGTCATTTGAGTACAGTGAGCTCATTGTCATGTTCAACGTAGTTGGACAGGTGTACCTAATAAAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38122
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 |
---|---|---|---|---|---|
ENSDART00000121498 | Nonsense | 217 | 929 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 35022080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 33489843 |
GRCz11 | 25 | 33975270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGACCAGTCTAAAATTTGTGTGTACAATATCGCTCAACTTTGAGAAA[C/T]AGATTCTGGCGATGGTACTTATATTCTATATTTTGTTTTCAGCTTGTGTG
Long Flanking Sequence:
TTTCGAAGCGTTTGATCGAGCTGGTGAGGAATGAAACGACAGAGTTTATGAAATACCTGCAAGAGGTTTCCAGATTGCATGCTGATGGGTACAACTACATGCCAGCAGATGCCATCCGCTACACTGAGGTATTCTTTATTAATTTTTTTTTTTATATATATATATTTTTTTTTTTATTAAATTTTTGTGCAAAAATGTGTAATTTTTTTGTATTTTTATGTTATAATTTTATCATTTATTTTATAATAATTGTAATAATAATAATAATAATAAACAATAATTTTATAAAAATAATATATTCATTATTTAATTTATTTAAGAATATTATTTACTTATTTATTTATTTATTTATTTGCTTATTTATTTATTTTCTTCTGCAGGAATATTTTACCGCCTGCTTGGATCATGTGAAGAGTTACCCACAGGTTTACGGTATTCAGGAGATTACAAGTCTGACCAGTCTAAAATTTGTGTGTACAATATCGCTCAACTTTGAGAAA[C/T]AGATTCTGGCGATGGTACTTATATTCTATATTTTGTTTTCAGCTTGTGTGAAACATACTGGTGTTTGTGTCATATCTTTTCTGTTTTTCTTCTCAGGGTAAAACAGACATGGTAAAAGAAAATGCGATACCGGCAAACACTCCACTTGCTGTAGATTATGAGAGTGTGGCCAAAGTGGTTCCTCCAGCTAAAAAAGCACATTCAGTACACAATGTAAGTACCAGTCTGTCATTGTGTGAGTAAAGAAAGAAACAGATTAATAAATAAAATATTTACATATTAAATATTCAATATATGTAATTAAATTTAAATGATTATTGTGTTTGTTTTTTTTTGCATTGTTATTATTTTGCATTGTTTAATAAAATATGGAAATTTTACAAAGAAAAATTTAAAAGAAATTCCTTTAAGTTCAGTAGAAACATTTATTTATATATGATTATATTTGATATATTATCGTCCTATATATTATGGATCATAAATACTATTTAAATGTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38123
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 |
---|---|---|---|---|---|
ENSDART00000121498 | Nonsense | 693 | 929 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 35035815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 33503578 |
GRCz11 | 25 | 33989005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTAATGGTGCGCAGCAGTGTGGACATCGCTCACCCGAAACACGACAGA[A/T]AGACCTTCAGGGTAACCCATGCACATACACATATGTTTGTATTGGTGGTT
Long Flanking Sequence:
CTGTGAGTTAACATGAACTAATAATGCACAACTGTTTTCGTTAACTAACATGAACAAATACTAATAATATGTGTATAATAATAACTGTGGTGTTTGTTGTTTGTTCATGTTAGTAAACGCATTAACATTAACTCATACAACCTTATTGTAAAGTGTTACCAATATACTATATAATGTTTATAATTGTATAATTATATATTTATGATATAATATTTACCATTTTTGTGCCTGTTTAGTTTTATTATTATTATTATTTTAATTTAAATATTGTTGTCAGATTCAGTGTGACGTTGATGTGTACAGAATATTCGTTTTATTATAAATATCGCTCGCTGTGTCTGTCAGGTCTTCTGCGGGAGTATCTTCAGGCCAGTGCTGAGGATGAGCTGGACTATGATCCTCCAGCAGAGGGCAGTGTTTTCTACAAACTCTACAGTCTGCTGGACGTCCTGCTAATGGTGCGCAGCAGTGTGGACATCGCTCACCCGAAACACGACAGA[A/T]AGACCTTCAGGGTAACCCATGCACATACACATATGTTTGTATTGGTGGTTTACGAGGACTCTCCATAGGCATAATGTATTTTATATGCTAAAAATGTGTATTATATAGCCTTACTCCACCCCTATTCCTAAATCCCACAAATTTGAATGGCAAAAGACCCTGTTTAGTATGATTTCTAACCATTATTAGGGTATGTCCTCATAACCCAGCTTAATAGTGTACAACTAGGTCATACCCATGTCGTTATACAAATTTTCTTGTAAACCACCAAAACCAATACACAGTTTCAGAAACACAAGTCTGCTTCTGGCCATGTAACCATCAGTCACATATTAGAGAATTCAAACCTCACCTACAATTGATTGTATTATTATTATTATTATTATTATTGTTGTTATTATTATTATTATTATTATTAGGTATAATATTATATGATAAAATTAATAAATGTATAGTTTGTCAGTGATTTTAAGCAACGTTTTGTTAACTTGATATCTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24715
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121498 | Nonsense | 853 | 929 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 35049676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 33517439 |
GRCz11 | 25 | 34002866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTTCCTTTGGACCCTACGCACGTCCTGCCATTTCATCAGAAACACAAC[A/T]GACCACCCTGCACCTTCCCTCCACGTCCACCCCCTCAGGTATGACCAGAT
Long Flanking Sequence:
TTATATTATACTATTCTACACTATATTATACTAAATTATACTTTATTATATTAAATTGTATTATATTATATTATTAGATTTTATTATATTATATTTTATTATATTATACTATATAATACTATTCTATACTATATTTTTATATATATTGTTTTTTACATTTTCATGTTGTGACCTCCTCAAGCTAAATGTTGTGTGTGTTTGACAGCTTGTCATCATCTGCAAATTATCCGTTCAGCTCTCACAGGTCTGTCAATAACACAATCTCTATCATCCTTGTGTCCTTTAACACCCACCCCAGGTTGCAGGAAGGTCGATACATGCTGGTCCACAAACCTCGTGAGGGATTTGTAACCATCTATAAAGCTAGCGATGAAGCAAAGGCTGTGCGCGGCGTGTTGAACTTACAGGCCACACACTGTGGAACCCCACCTGTACCTCCAGGAGTCCCTTGGGTTCCTTTGGACCCTACGCACGTCCTGCCATTTCATCAGAAACACAAC[A/T]GACCACCCTGCACCTTCCCTCCACGTCCACCCCCTCAGGTATGACCAGATTTTCTCGTAAAAAATACAGACTTGCTGTAGATATTGTGTACTCTGTGGTGCTTATTTGGGAAAATTGGGATCGAATTAAGCTTGCAACATAGTTTTAGTCTAGCATTTTCAGAGGTTGTGTGATGAAGATGTTATAACTTAGAGTTGGTCATTTTGATTTGAATGTTGCAGGTGTAACATTTCTAAATGTTAAGCCTTGGTGCTTATGTTAGAAAATTGGGATCGATTTAAGCTTGCAACGCATATTTCAGTCTGAAATATATCAAATGTGTTGAAGAGTGGTGCTTGTGTTGGAAACATTGGTTTGGTAATTGCTCATTTTAGTGGTTGTTGGGTTGCTCGTCTTCTCAAGACGTTGAATTGTGGTGCTTATGTGGGAAATTTAGGTTTGAGTTTAGCCTGTATCTTGTTTCTTTATCTAGTATTTCTAGGGAAGGTGTGATGTAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38124
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 |
---|---|---|---|---|---|
ENSDART00000121498 | Nonsense | 874 | 929 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 25 (position 35054985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 33522748 |
GRCz11 | 25 | 34008175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCTCCTTTTCTATTCTCATACAGCCAAAAGTTAAGGCGGGACCAAAG[C/T]AAAGACAGAGAAAAAAAGCTTGCAGACAACCACAAAAAAGCAACGCATCA
Long Flanking Sequence:
CAGGGCATTAAATCACTGTTCATTTCTTTGCATTTTAACTTTGTAAACTATAAACTCATGCGTCTCCTCACGGTTTGTCTCATTTTGTGAGCTAGCTTCGTTCGCTCACGTTCTCCCCTGCTGGCCACGCCCACTCCTGCCCGATGCCCGCGGAGCTCCACGCCCATTAATCATGCATCTTTTGAAAAAATTCTGAAGTAGACTTTAACCGAAAGTGGGGGGTGTCATGGCCCTTTAATTGTGGTGCTTATGTGGGAAATTTGGGTTCAAACTTTTTTTGGGATCTTGTGTCCATTCCTGTAAAAAAAAAAATGCATCTTCCGCATATTTTGACAGTATTCTGTTACAATATCGTGCAGCCCCTAACGTTCACTATTAAGATTTGAACCTACAATCTTAACCACTGCCATATATAGTAGTGATATTATGTTACCCCTTATCAAAAGTAACTTTTCTCCTTTTCTATTCTCATACAGCCAAAAGTTAAGGCGGGACCAAAG[C/T]AAAGACAGAGAAAAAAAGCTTGCAGACAACCACAAAAAAGCAACGCATCAGCCAACCCCAATGACTCGCCAAAGACGAAGAAGAAACAAGCTGCTCGTATGAAGCTATCATTGCTGGACAACATGAGGGACAAGCTGCTGAAGGACCTGCAGACCAGTGAAGATGAATAGACCCTCGTCTTGATGTGTTGTTGTTTTGGTTTGTTCTTAAGCACTTAGCATAAATTGATATGCTTTACAGCAAACATAATAATAGTGTGTAGACAGTAAATGTGTGACCAAGTTTTGTATTATTTTTGGCAGAAGAAGATAAAAGTATTTTTTAAATAAAAAAAATGTTATTATTAATATTAGCGCCATGTTTTGGGTTTATATCCTGGTGTGTTTTCGAAGGATTTGTGTTTGCAATTAGTTTTCTAAAAAAATATGTTTAGAATTGACCCTTTGCTAAGCCACACCCAAAAACCGCCACCCACTAATCGTGGCTTAGCAACTGTAGCT
Associated Phenotype:
Not determined