ZMP
si:ch211-213a13.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LXX1]
Human Orthologues:
NLRP12, RNH1
Human Descriptions:
NLR family, pyrin domain containing 12 [Source:HGNC Symbol;Acc:22938]
ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:10074]
ribonuclease/angiogenin inhibitor 1 [Source:HGNC Symbol;Acc:10074]
Mouse Orthologue:
Rnh1
Mouse Description:
ribonuclease/angiogenin inhibitor 1 Gene [Source:MGI Symbol;Acc:MGI:1195456]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32373 | Nonsense | Available for shipment | Available now |
sa37423 | Essential Splice Site | Available for shipment | Available now |
sa44982 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32373
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 |
---|---|---|---|---|---|
ENSDART00000106028 | Nonsense | 1253 | 1522 | 23 | 28 |
ENSDART00000145430 | Nonsense | 70 | 282 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 9097280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 9128356 |
GRCz11 | 22 | 9158038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAGATCCATTTCTTGTGAGAGAGCTAAATCTGCGTGATCAAAAACTC[G/T]GAGACACAAACATCAAATATCTTGCTGCTCTGCTGCAGGATAAACACTGT
Long Flanking Sequence:
TTTCAGTCATTTTTAATAATACTTTAAATCTATTTCCTCTAGTCTTTCAGACTGCAGTATCAGTGAAGAAGGTTATAAAGCTCTGGCTTCAGCTCTGAGATCAAACCTTTCACATCTGATAGAGCTGGATCTCAGAGGAAATGATCCTGGACAATCAGGAGTGAAGGAGCTCACTGACTTACTGGAGGATCGATACACTAAATTGAAGACTCTCAGGTGAAACATGAAAAAAATATATATTTTCCAGCTGATTATTTAAAACAGAAATGATATAATATGTTGCGTACAGTATACATTGATTTTAGGATTTAAAAATAATAATAAAATATTTTAATATAATTTTCATTAAGCCACATAAGGTCAGTGAACTGCATTCAGCTCTGCTTCTAATTTACAGGTTTTTAAGTCCTGATGCAGAAAAGGCTTGTAAGTATGTGCCTGGACTTGTTGGTAAAGATCCATTTCTTGTGAGAGAGCTAAATCTGCGTGATCAAAAACTC[G/T]GAGACACAAACATCAAATATCTTGCTGCTCTGCTGCAGGATAAACACTGTAAACTCAACACAATTCAGTGAGTATATTACAGGGATTACTAGTTAAATATTTTACCAGTGTAGCTGTTGATGCTTATATGTCCTCATTTATCAGGACTGCAATTAGCATCTACATTTAGAACAGACAACATAACAATACAAGTAGTTATGAATGAACAAACAATGAACAATACATGTACAGCATTTATTAATCATATTCAGCATTCAAATCAAACTCTGTGCTTGTTAACATTAGTTATTGCACTTTGAGTCAACATGAACTAACAATGAACAACTGCATTTACATAAACAGACATGAACAAATACTTTAATAAATGTATTGTTCTTTGTTTGTTTGTTAGTAAAAACATTAAGCAACATTAAAAACGTGTCCTGTATTGTAAGGTGTAAGCTATATTGGTTTAACAAAAAGAACTGGCATCAATCTGTAAATAATTGTCTAAATGAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37423
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 |
---|---|---|---|---|---|
ENSDART00000106028 | Essential Splice Site | 1275 | 1522 | 23 | 28 |
ENSDART00000145430 | Essential Splice Site | 92 | 282 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 9097211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 9128287 |
GRCz11 | 22 | 9157969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTGCTGCTCTGCTGCAGGATAAACACTGTAAACTCAACACAATTCAG[T/A]GAGTATATTACAGGGATTACTAGTTAAATATTTTACCAGTGTAGCTGTTG
Long Flanking Sequence:
AGGTTATAAAGCTCTGGCTTCAGCTCTGAGATCAAACCTTTCACATCTGATAGAGCTGGATCTCAGAGGAAATGATCCTGGACAATCAGGAGTGAAGGAGCTCACTGACTTACTGGAGGATCGATACACTAAATTGAAGACTCTCAGGTGAAACATGAAAAAAATATATATTTTCCAGCTGATTATTTAAAACAGAAATGATATAATATGTTGCGTACAGTATACATTGATTTTAGGATTTAAAAATAATAATAAAATATTTTAATATAATTTTCATTAAGCCACATAAGGTCAGTGAACTGCATTCAGCTCTGCTTCTAATTTACAGGTTTTTAAGTCCTGATGCAGAAAAGGCTTGTAAGTATGTGCCTGGACTTGTTGGTAAAGATCCATTTCTTGTGAGAGAGCTAAATCTGCGTGATCAAAAACTCGGAGACACAAACATCAAATATCTTGCTGCTCTGCTGCAGGATAAACACTGTAAACTCAACACAATTCAG[T/A]GAGTATATTACAGGGATTACTAGTTAAATATTTTACCAGTGTAGCTGTTGATGCTTATATGTCCTCATTTATCAGGACTGCAATTAGCATCTACATTTAGAACAGACAACATAACAATACAAGTAGTTATGAATGAACAAACAATGAACAATACATGTACAGCATTTATTAATCATATTCAGCATTCAAATCAAACTCTGTGCTTGTTAACATTAGTTATTGCACTTTGAGTCAACATGAACTAACAATGAACAACTGCATTTACATAAACAGACATGAACAAATACTTTAATAAATGTATTGTTCTTTGTTTGTTTGTTAGTAAAAACATTAAGCAACATTAAAAACGTGTCCTGTATTGTAAGGTGTAAGCTATATTGGTTTAACAAAAAGAACTGGCATCAATCTGTAAATAATTGTCTAAATGAGACTAAATTAAATAAGAGTATTCTGATTATAATTAACTCTGATCTACTTATTTTAATTGAAAATTATATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44982
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 |
---|---|---|---|---|---|
ENSDART00000106028 | Nonsense | 1313 | 1522 | 24 | 28 |
ENSDART00000145430 | Nonsense | 130 | 282 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 9096435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 9127511 |
GRCz11 | 22 | 9157193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCATCACACCTGAGAGAACTGGACCTCAGTGAGAATCAAATTAAAAAC[A/T]GAGCAGTGAATCTCTTATGTGACGTACTGAAAGATTCACACTGTAAACTG
Long Flanking Sequence:
ATGAACAAATACTTTAATAAATGTATTGTTCTTTGTTTGTTTGTTAGTAAAAACATTAAGCAACATTAAAAACGTGTCCTGTATTGTAAGGTGTAAGCTATATTGGTTTAACAAAAAGAACTGGCATCAATCTGTAAATAATTGTCTAAATGAGACTAAATTAAATAAGAGTATTCTGATTATAATTAACTCTGATCTACTTATTTTAATTGAAAATTATATTATCTCATTAGATCAGTCCAATAATGAGCAGGTATCAACTTTTTTGCGCTATATAAACATTGTATACTGGAAAAAAATCTGTAATATCCAGACATTTGTTTGCAACACTTTTTTCGGTCATAGTGAATCTTGAGCTTTTGTTTCTGTGCTTTTAATTTTATTTTAGGCTGCTTAAATGCAGTATTACAGAGGAACAGTGTGTGATCCTGACTTCAGCTCTGAAATCAAACCCATCACACCTGAGAGAACTGGACCTCAGTGAGAATCAAATTAAAAAC[A/T]GAGCAGTGAATCTCTTATGTGACGTACTGAAAGATTCACACTGTAAACTGGAGACACTGAGGTGAGAGACATTCACAAAACAAGAAAAAATATCCTTTTATCTGTTATAGTTTATAAAATAGTAATAGAAATATGACAGTAGCTAATTTAAACTTTGTCAGAATAAATTCATCTTGATAATAGGTTAACAGTTAAGAAAGGTACAGTGTAATTGGATTACAATCAGTCAAATATAATTCAGACAACTGTTAGTATGTCAACACCAGTGTTGGGTGTAATTGGCTACAAAGTAACGAGTTACTGTAGTTAAATCACTTATCTGCTGAATAAGGAAGAGATTAGTTTTTTTTATATCATTTAATTACAGTTGTTTATAACTGACAAACCATTAATTTGTTAGAAATAAATGACACTATATGGTATGTATGAAATGTTTGGGAATTAATTTGAAATGTTTCATGTTTTGATGCATATTATGTTTAACTTTTTATAAGTATTAC
Associated Phenotype:
Not determined