ZMP
si:ch211-255g12.8
Ensembl ID:
ZFIN ID:
Description:
Novel NACHT domain containing protein [Source:UniProtKB/TrEMBL;Acc:B0R1B7]
Human Orthologue:
NLRP6
Human Description:
NLR family, pyrin domain containing 6 [Source:HGNC Symbol;Acc:22944]
Mouse Orthologue:
Nlrp6
Mouse Description:
NLR family, pyrin domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:2141990]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41114 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7119 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41114
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 |
|---|---|---|---|---|---|
| ENSDART00000101466 | Nonsense | 561 | 984 | 3 | 7 |
| ENSDART00000133606 | None | None | 254 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 7456143)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6842946 |
| GRCz11 | 8 | 6886494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTGCGCTTTCTGCTGGGTATCTCACTGGAGTCCAATCAAAGACTCCTA[C/T]AGGGTCTCCTGAGGCATACGGAGAAGAGCTCAGAGAGCATCAGGACAATC
Long Flanking Sequence:
TGACTGAAATGTACATTCATTTCCTGCTCATCCAGACTAAAATAAAGAACCAGAAGTATGCTGAGAATGATCAGAGAAATCCAGAAGAGCTTCTACAGTCCAGCAAAGATGTGATCTTGAAACTTGCTGATCTGGCCTTCAAACAGCTGATGAAGGGCAATGTGACATTTTACGAGGAGGACCTAGGAGAGCATGGCATAGATGTTACAGAGAGCTCAGTGAATTCTGGGATGCTCACTGAGATCTTCAGGTTGGAGTCTGTGATTCATCATCAGAAAGTCTACTGCTTCATACATCTGAGCTTTCAGGAGTTTCTCGCTGCGTTTTACATCTTTCACTGCTTTGTAAACGACACTTCAGAGGCTCTGAAAGTGTTTGATTTGCTCTCAAATTTTTATAAGGGAGTGGTAGACGCAGCTCTTCAGAGTGAGAATGGACACCTGGATCTGTTCTTGCGCTTTCTGCTGGGTATCTCACTGGAGTCCAATCAAAGACTCCTA[C/T]AGGGTCTCCTGAGGCATACGGAGAAGAGCTCAGAGAGCATCAGGACAATCGCAGCTTACATTAAAGAGAAAATCAAACACGAGCAGGGGATTTTAGCTGACCGATCCATCAATCTGTTCCTCTGTCTGCTGGAGATAAAGGATCAAACCCTGTCCAGAGAGATTCTGGAGTTTCTGAAATCCGACAAACACTCAGAGAATAAACTCTCTCCTGCTCACTGCTCGGCGATCGCCTACATGCTCCAGATGTCAGAGGAGGTGCTGGAGGAGCTGGATCTCCGAAAATACAACACGTCAGATGAGGGACGGAGAAGACTGCTGCCGGCAGTAATGAACTGCAGAAAAGCACTGTGAGTGTCTCTTTGAATTTACGTATTATCTGTAAAAAGCATTTAGTTGCTTTTTTTTTAAATGGTGAGTAAACCTGTTGCCTTAAACGTGACAAGTTGACTTAAAAAAGTGAGTAAATCCATTGCAAGTTAGAACCTTTGAGTTGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7119
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101466 | Nonsense | 934 | 984 | 7 | 7 |
| ENSDART00000133606 | None | None | 254 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 7450130)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 6836933 |
| GRCz11 | 8 | 6880481 |
KASP Assay ID:
554-4835.1 (used for ordering genotyping assays)
KASP Sequence:
AGTATAGACATACTTGTCCATTCAGACTCCTCAAACAGAATAGCAGTGTA[T/A]CTGGACAGGCCRGCTGGAATCCTGTCTTTCTACAGTGTCTCTGATRAACA
Long Flanking Sequence:
AACGTTTAAATACACAAATAATGGATGAAATATAAGTATTATGCCATGTAATGAGATGTTATAGCCATGAAATATTACAATGACAGAACTGTATTTGTTGTCCTCTCTCTCTTCTTATGTGCAGATTCCTGCTGTCTCAGTCTAGATCCAGACACAGCAAACACTCGCCTCACTCTTTCAGAGAGAAACAGAATGGTGATGCGTGTGGTAGATGAGCAGCCCTATCCTGATCATCCAGACAGATTTGAGCACTATGAGCAGGTGCTGTGTAAAGAAACTTTGTCTGATCGTTGCTACTGGGAGGCTGAGTGGAGTCGGGGGGTAAATGCTGCAGTGGCATATAAAGGAATCCGAAAAAAAGGTGGGAGTGACTGCAGATTTGGGTGGAACGAAAAGTCCTGGGGTCTTTTCTGTACTCCGGATCGATACAGTGCTTGGCACGATTATAGGAGTATAGACATACTTGTCCATTCAGACTCCTCAAACAGAATAGCAGTGTA[T/A]CTGGACAGGCCGGCTGGAATCCTGTCTTTCTACAGTGTCTCTGATGAACACACACTCACACACATACACACGTTTAATGCCAAGTTCACTGAACCACTCTATGCTGGATTTTCTGTTTATGGTTCAGTGTCAATAGCGGGGTTTCCATCCTAATGTGAAGCAAATCTTTCCAAATTAAAAAAAAAAAGAAAGTTCCCCATTGCAAAGTAGCTGCTTTTACCTCAAGTTAGAGTGGCTTGTTATAGTATTGGTGACCTAGTAACCAACAGTTACAAACAAGGCAAGCATAATGGAGTCATGTGAGTGTAATGTGTTTATTAGTCATTATTAGTGTTTCCATCTTACATTATTTACATTAACCCTTTATGCAAAACCACTGCATGTTAGCGTAAAAACTACATTCAGTCATTTTCTTTTTGGCTTAAGGCTGATTTATACTTCTGCGTCAAACGCACGGGTATGCTACGGCGTTGACGAATAGCCCTTCGCCGTGGCCGTCG
Associated Phenotype:
Not determined