ZMP
si:ch211-11p18.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1MTF4]
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 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24078 | Nonsense | Available for shipment | Available now |
sa32376 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24078
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000141242 | Nonsense | 50 | 207 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 22 (position 9351140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 9382216 |
GRCz11 | 22 | 9411898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGATGAAGCCTGTCAGTTTGTGACTGGAATTGTGGGTAAAAACCTGT[T/A]ACTCCTGAAAGAACTGAATCTGAGTGATCGTCAACTAGGAGACACACGAG
Long Flanking Sequence:
CATTTTGATTGCATTATTGTTGTCATGAATTTTATTGTTAAAGTAACAGTTCATAAACAGTTTAAATGTATATACTGATATTGTTTCATTTTCATAAAACTGAAATCCCTATTACAGTCTTTCAGACTGCAGTATCAGTGAAGAAGGTTATAAAGCTCTGGCTTCAGCTCTAAGATCAAACCCTTCACACCTGATAGAGCTGGATCTCAGAGGAAATGATCCTGGACAATCAGGAGTGAAGGAGCTGATAGAGTTACTGCAGGATCCACTCTGTACACTGAAGACACTGAGGTAACATTTGAATAAAAACATGCATATGAAATAATAACAAACATGTTGTGTTACTAATGCCACATTCAGCACAATTTATTGTTGTATCAGAGTTAAAGTGATTAACAAAAATCAGTTTATTTTCCTTTTTCATTTTTTCTTCAGGTTTTTGAGTCCTGCTGCTGATGAAGCCTGTCAGTTTGTGACTGGAATTGTGGGTAAAAACCTGT[T/A]ACTCCTGAAAGAACTGAATCTGAGTGATCGTCAACTAGGAGACACACGAGTGAATCAACTCTCTGCTCTACTGCAGGATAAACACTGTACACTCAACACACTCATGTGAGTATTGTGTAATCTGTTAAAATGACAATTACATTTTCAATTATTTGCTTTGATCTTGTTTTTTCTCAATTTTTAAATGAATTCAATCTCTTTGTTTTCTTTCTCTTCAGGCTGAATAATAACAGGATTACAGCAGAAGGTTGTGCTGCTTTGACTTCAGCATTTAATTTAAATCCATCAAACCTGATGGAGCTCACTCTGAGTGGAAATAAACTAGAAGACTCAGGAGTAGAAAAGATCTGTTCTCTGCTGAAAAATACACAGTGCAGATTGAAGAAACTGAGGTCTGTATTTTATTTTATTTTAATATTTTATTTTATTTTATTCTATTTTTTGTAGATGTCTGCATGTAAGTATACAACTATATTTATGTGTAATGTATTGTGCATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32376
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 |
---|---|---|---|---|---|
ENSDART00000141242 | Nonsense | 121 | 207 | 3 | 4 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 9351465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 9382541 |
GRCz11 | 22 | 9412223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAAATCCATCAAACCTGATGGAGCTCACTCTGAGTGGAAATAAACTA[G/T]AAGACTCAGGAGTAGAAAAGATCTGTTCTCTGCTGAAAAATACACAGTGC
Long Flanking Sequence:
TAACAAACATGTTGTGTTACTAATGCCACATTCAGCACAATTTATTGTTGTATCAGAGTTAAAGTGATTAACAAAAATCAGTTTATTTTCCTTTTTCATTTTTTCTTCAGGTTTTTGAGTCCTGCTGCTGATGAAGCCTGTCAGTTTGTGACTGGAATTGTGGGTAAAAACCTGTTACTCCTGAAAGAACTGAATCTGAGTGATCGTCAACTAGGAGACACACGAGTGAATCAACTCTCTGCTCTACTGCAGGATAAACACTGTACACTCAACACACTCATGTGAGTATTGTGTAATCTGTTAAAATGACAATTACATTTTCAATTATTTGCTTTGATCTTGTTTTTTCTCAATTTTTAAATGAATTCAATCTCTTTGTTTTCTTTCTCTTCAGGCTGAATAATAACAGGATTACAGCAGAAGGTTGTGCTGCTTTGACTTCAGCATTTAATTTAAATCCATCAAACCTGATGGAGCTCACTCTGAGTGGAAATAAACTA[G/T]AAGACTCAGGAGTAGAAAAGATCTGTTCTCTGCTGAAAAATACACAGTGCAGATTGAAGAAACTGAGGTCTGTATTTTATTTTATTTTAATATTTTATTTTATTTTATTCTATTTTTTGTAGATGTCTGCATGTAAGTATACAACTATATTTATGTGTAATGTATTGTGCATTTTATTTTCACAAAATCACAAACACACAAAATTTATTACAAAATGTCTGTATGATCAGATTAAAAATAAGTTTTAGATTACTCTGATACGTGCAATTTTCATGGCTACTTCAAGCTTTAAATATAATTTGTTATATTTATATGTCTAAACAAAACTGGTGTTATCATTTAAAAATTGATTGCCAGGCTTGACAGTTTTTCTTATATCTAGTCTTTCAGACTGCAGGATCACTGAAGAAGGATATAAAAGTTTGACTTTGTCCCTGAAGTCAAATTCACACCTGATAGAGCTGGATCTCAGAGGAAATGATCCTGGACAATCAGGAGTG
Associated Phenotype:
Not determined