ZMP
NPR1 (2 of 2)
Ensembl ID:
Description:
natriuretic peptide receptor A/guanylate cyclase A (atrionatriuretic peptide receptor A) [Source:HGN
Human Orthologue:
NPR1
Human Description:
natriuretic peptide receptor A/guanylate cyclase A (atrionatriuretic peptide receptor A) [Source:HGN
Mouse Orthologue:
Npr1
Mouse Description:
natriuretic peptide receptor 1 Gene [Source:MGI Symbol;Acc:MGI:97371]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36166 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12864 | Nonsense | Available for shipment | Available now |
sa16937 | Nonsense | Available for shipment | Available now |
sa42742 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44853 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36166
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 |
---|---|---|---|---|---|
ENSDART00000018213 | Nonsense | 383 | 1070 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 16 (position 31171408)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29008597 |
GRCz11 | 16 | 28943220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGCTGTACTGCCATGCTTTAAATGAGAGCCTTTCAGACAGCCATGAA[C/T]GACCTTCAGGAGAGTCTGTCAGCAAACGAATGTGGAACCGGACCTATTAT
Long Flanking Sequence:
AAATTAAATGTGATTTTACTCAAAACAAGAACAAACCTGCCAATGCAGTTAGAAAAATAATCTTCTTTACTTTTGAGTTTTCTGACCACATTGTCATGTTCTGTACTTGTTTTTGTTTTAAAACAAACTCATTTATATTTTAACCAGTTTTTTCAGACAGCAAGACTAAAATAAAAATATAAAATTATTAATTAACAATAAAGTAGTTTTGCTTCTCAAATAAATGTGTGTTGATTTCAGAATGTTTAGATATGTGTGTAGAATGAACAATCATTTTGCCGTCATTTTTATTTATTTTGCTTCTGTAATTATATCTTGATTTAAGAACATTTAGATTATTGTACTATAATACTGAGATAAAACATACATTTTCATTTTCCTGTGTTTTAACTTGTTTGTGTATTTGATTCTTTCAGATGAACATCATCTCTGGGGGTTTCTATGATGGTCTGATGCTGTACTGCCATGCTTTAAATGAGAGCCTTTCAGACAGCCATGAA[C/T]GACCTTCAGGAGAGTCTGTCAGCAAACGAATGTGGAACCGGACCTATTATGGTGAGTACATGATCCAAATGAAATGGATCATTGTCAAATGTGACATTACATTAATATGTTATACAGAGACTTTTTTTATCTTAAAACCTTGACTTAATGGCCCATTTTAACTACAGTATGTGCAAATTTATGGGAGGGATTGATTTAATGTTTGGACCCTCCTGTAGAAAGTCAAAACTACGTGTATGGTGGTCTGGAAAATGTTTTCAGTGATCTGTTAGTGAGATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAAGTTAATATAAATATGAATTTGTATTTTATTCACAATACTATTAAACAATACTATTATAGTTCACAATATTATTAAATATTACAATTGTAACAACATCAACAGCAGCGCACGTGCACAATATGCAGCTGATTCTGTGGTTGACGAGCGACATAAAAAGCGCAGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12864
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018213 | Nonsense | 398 | 1070 | 4 | 21 |
ENSDART00000018213 | Nonsense | 398 | 1070 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 16 (position 31171455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29008644 |
GRCz11 | 16 | 28943267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACGACCTTCAGGAGAGTCTRTCAGCAAACGAATGTGGAACCGGACCTA[T/G]TATGGTGAGTACATGATCCAAATRAAATRGATCATTGTCAAATGTGACWT
Long Flanking Sequence:
GTTAGAAAAATAATCTTCTTTACTTTTGAGTTTTCTGACCACATTGTCATGTTCTGTACTTGTTTTTGTTTTAAAACAAACTCATTTATATTTTAACCAGTTTTTTCAGACAGCAAGACTAAAATAAAAATATAAAATTATTAATTAACAATAAAGTAGTTTTGCTTCTCAAATAAATGTGTGTTGATTTCAGAATGTTTAGATATGTGTGTAGAATGAACAATCATTTTGCCGTCATTTTTATTTATTTTGCTTCTGTAATTATATCTTGATTTAAGAACATTTAGATTATTGTACTATAATACTGAGATAAAACATACATTTTCATTTTCCTGTGTTTTAACTTGTTTGTGTATTTGATTCTTTCAGATGAACATCATCTCTGGGGGTTTCTATGATGGTCTGATGCTGTACTGCCATGCTTTAAATGAGAGCCTTTCAGACAGCCATGAACGACCTTCAGGAGAGTCTGTCAGCAAACGAATGTGGAACCGGACCTA[T/G]TATGGTGAGTACATGATCCAAATGAAATGGATCATTGTCAAATGTGACATTACATTAATATGTTATACAGAGACTTTTTTTATCTTAAAACCTTGACTTAATGGCCCATTTTAACTACAGTATGTGCAAATTTATGGGAGGGATTGATTTAATGTTTGGACCCTCCTGTAGAAAGTCAAAACTACGTGTATGGTGGTCTGGAAAATGTTTTCAGTGATCTGTTAGTGAGATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAAGTTAATATAAATATGAATTTGTATTTTATTCACAATACTATTAAACAATACTATTATAGTTCACAATATTATTAAATATTACAATTGTAACAACATCAACAGCAGCGCACGTGCACAATATGCAGCTGATTCTGTGGTTGACGAGCGACATAAAAAGCGCAGCACCCTTCTTTTTTTTCTTGTTAGAAAAAAGGCAATGTGGCAAATGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16937
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018213 | Nonsense | 398 | 1070 | 4 | 21 |
ENSDART00000018213 | Nonsense | 398 | 1070 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 16 (position 31171455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29008644 |
GRCz11 | 16 | 28943267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACGACCTTCAGGAGAGTCTRTCAGCAAACGAATGTGGAACCGGACCTA[T/G]TATGGTGAGTACATGATCCAAATRAAATRGATCATTGTCAAATGTGACWT
Long Flanking Sequence:
GTTAGAAAAATAATCTTCTTTACTTTTGAGTTTTCTGACCACATTGTCATGTTCTGTACTTGTTTTTGTTTTAAAACAAACTCATTTATATTTTAACCAGTTTTTTCAGACAGCAAGACTAAAATAAAAATATAAAATTATTAATTAACAATAAAGTAGTTTTGCTTCTCAAATAAATGTGTGTTGATTTCAGAATGTTTAGATATGTGTGTAGAATGAACAATCATTTTGCCGTCATTTTTATTTATTTTGCTTCTGTAATTATATCTTGATTTAAGAACATTTAGATTATTGTACTATAATACTGAGATAAAACATACATTTTCATTTTCCTGTGTTTTAACTTGTTTGTGTATTTGATTCTTTCAGATGAACATCATCTCTGGGGGTTTCTATGATGGTCTGATGCTGTACTGCCATGCTTTAAATGAGAGCCTTTCAGACAGCCATGAACGACCTTCAGGAGAGTCTGTCAGCAAACGAATGTGGAACCGGACCTA[T/G]TATGGTGAGTACATGATCCAAATGAAATGGATCATTGTCAAATGTGACATTACATTAATATGTTATACAGAGACTTTTTTTATCTTAAAACCTTGACTTAATGGCCCATTTTAACTACAGTATGTGCAAATTTATGGGAGGGATTGATTTAATGTTTGGACCCTCCTGTAGAAAGTCAAAACTACGTGTATGGTGGTCTGGAAAATGTTTTCAGTGATCTGTTAGTGAGATGATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAAGTTAATATAAATATGAATTTGTATTTTATTCACAATACTATTAAACAATACTATTATAGTTCACAATATTATTAAATATTACAATTGTAACAACATCAACAGCAGCGCACGTGCACAATATGCAGCTGATTCTGTGGTTGACGAGCGACATAAAAAGCGCAGCACCCTTCTTTTTTTTCTTGTTAGAAAAAAGGCAATGTGGCAAATGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42742
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018213 | Essential Splice Site | 655 | 1070 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 16 (position 31199143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29036332 |
GRCz11 | 16 | 28970955 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACACTAGATTGGATGTTCAAATACTCATTAATCAGCGACATAGTAAAG[G/A]TAGAAACCCCTTTCTGTATTTTGTTAATGATGAAATTCACGTTAAAGGCA
Long Flanking Sequence:
TGTTGAAAGCTCAGGTATGTTTAAAGTCACAGTCACAATTGTAAGAAATGTGTTCAAATTGTAAGATGTAAACTTAGAATTGCAAAAAATGCATTCGAATATGTCTCAAATCTGAATTGTACAATTTATTTTGTAGGACTTTTTTCCATATGAACAACTTTGCCAAAGAACTTGCCTAGTGTGTGTTTGGCAGAAGTATTTAGACTGTTTACATTCATTTAGATGGAATCAGGCATTCTTGATATTTTGTAGAATAATATAGAAAGTACATTTTTATTTCTCAAAAAATGTGTCCCCAACTTAAGTTTAAATGTACAAAAAATACACAGACACACACAAAAAGAATTTAATATTTGCATGCTTTAAAAATCATTTAGCAATTTAGCACTGAAATTGTACATCTCCGAATTTCTGCATCTTTTTTACAGAATATTTTGGAGAACGACAGCATTACACTAGATTGGATGTTCAAATACTCATTAATCAGCGACATAGTAAAG[G/A]TAGAAACCCCTTTCTGTATTTTGTTAATGATGAAATTCACGTTAAAGGCATAGTTCACCCAAAATTTCAAAATCTGTCATCATTTTCTCACCCTCCACTTGCTCCAAACTTTCATGAATTTCTTTTTTCTATTCAACAAAAAAGGACAAAATATGAAGAACATAATATATCACATCAATTCTTTTTATTCTACCATGAATTTCAATGGCTGCCATTTTCAACATTCTTCAAAATCCTTTTTTGGATGACAGAAGAAAGAAGCTCATAAAGCTTTGGAATCACTTGAAATTGATTAGACGTTAAATAAATGTTTATTTTTGGGTGAACCATCTCTTTAAATGTTTATTTTCCATTCTCCCTCATTGCACTGCATCCTTATCCTCCTGCTTTCCTTCATACTGCCCAATCTGTCTCTCCCCTCAGGGCATGGCTTTCCTTCATAACAGTGTGATTGTATCCCATGGCAACCTGAAGTCTTCCAACTGTGTGGTTGACAATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44853
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018213 | Essential Splice Site | 989 | 1070 | 19 | 21 |
Genomic Location (Zv9):
Chromosome 16 (position 31215039)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 29052228 |
GRCz11 | 16 | 28986851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCACCGACCCGATGAGCAACTCAAATTACGAATCGGCATTCACAGTGG[T/C]GAGAATGAGCATTTTAAACAGTTTTTTTGACACTAACAGGGAATTTTCTT
Long Flanking Sequence:
GTGATTTTTTCTTTTGTCCTGTGCTTTGTGCTGAAGTAAATCTCCACCTGCTATACTAGTGCTAAACAATGTCTAAAATAATCAGTAAATATTAAAACTTGAAGCCAAGGGTGTTTACACAATGGTGTTTACATCCAAGAACTGAAAACATTTAATGTATTTTGGCTGTTTTCTATAAAGTGCACGAGTTTGAATTTGATGAATTATCTTCTCTACCTATGCATATTACAGTATGTGTTCAGTCTATAGGCATGTTTAATACAACTTTGACAGACTACATATATATATATTTCATATATCATTTTTGTTTTATTGTTCCTTTAGGTGGAGACAATAGGCGATGCTTACATGGTAGTTTCAGGACTGCCGGTACGAAACGGCAAACTGCATGGTCGTGAGATTGCACGGATGTCCCTCGCTCTGTTGGAGGCTGTCAAAACATTTAAGATTCGCCACCGACCCGATGAGCAACTCAAATTACGAATCGGCATTCACAGTGG[T/C]GAGAATGAGCATTTTAAACAGTTTTTTTGACACTAACAGGGAATTTTCTTGTATTGAACTATGTTTATCTAACATAATACTAAACATTACTAAATACTAAATGCTAATAAATATTCATATTTATTAATATTACAAAATATTAGTAATAAAATTGTTCTAACATACTAAACCTGGTTTTAGCATATGAAGTTTTGAGTATTGAGAATTGTGTGTTTTGTTTGTGTCTGTGTGTATGTTCCAGGCCCTGTATGTGCAGGTGTAGTTGGGCTGAAGATGCCTCGGTATTGTCTTTTCGGAGATACTGTAAACACATCTTCTCGTATGGAGTCGAATGGAGAACGTAAGAGAAAAAATTATCTCTATCCCACCAAACACTTTAAAACTTAAAGGTCCCATGAAGTGCTGTGAAATGTGCATTTTTTATTAGCTGTTTGACGTAATCTCAACTGAAAAATTATGGGAGAGTGGGACATAAAATAGCTCCTCAGCTTTTTAAAAAC
Associated Phenotype:
Not determined