ZMP
si:dkey-240n22.1
Ensembl ID:
ZFIN ID:
Description:
Novel NACHT domain containing protein [Source:UniProtKB/TrEMBL;Acc:B0S5A0]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44596 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40340 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38445 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44596
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000133855 | Nonsense | 26 | 107 | 3 | 5 |
ENSDART00000134357 | None | None | 975 | None | 7 |
ENSDART00000135345 | Nonsense | 26 | 527 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60965162)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75445961 |
GRCz11 | 4 | 77022699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTTGTCTCTTCAGTGTGAGATCAGGATCATGTGTGAAGAGTGACTG[G/A]TCTAAAGAGGATCCACCAGAGTTCAGTGAGGAAACACCATCACCTGCCCA
Long Flanking Sequence:
ATGATGGACAAAGCTTCAGTTTACACCTTCAGGAAATGTTTTGAGAGTGTTCCGAGGTGTATGCGATGCTTTTAATGCGCACACCTCTCCATATGACATAATCACGCCACCGCTAACCCGACCCCTCACAGTGACGTCACTACCTCCACTGAGTGCAGTCTCAGCTTGCTCATGCAAGGCTGTATCCAGATACTATTGAATGTGTTGAGATCATTGTAGGTTATAAACAGCTTGGTCTGGTGTCATATTTACCAGAGCTGAATTTACTTAATTTGTCAAGTTATAAGACCTGTACAACATTAGAATTAACCGCAGAACAGTTTCAGCAGACCTGATCAGACAGACCTTCAGTCAACTATTAGTTAGTGCTAAATTAAACTGAGCAAACTCATATTTGGCTGATAAACTCTCAAAGGAGATTGAAGTTTGTCCTGCAGTTTATTCCTCTTGTGTGTTTGTCTCTTCAGTGTGAGATCAGGATCATGTGTGAAGAGTGACTG[G/A]TCTAAAGAGGATCCACCAGAGTTCAGTGAGGAAACACCATCACCTGCCCAAAGGTATTTTGGTGTTTTACATGCACTTCAAAGTATGTTGAAATTGGTTGTACTATTGGACAGCTAACGATTGAACTGATGGACTGTGCCTGTCAGGACTCCTGTTAGGTTGTGGTATTGTTTTGGCATTGTTTTGCCTCTACTACCGTGCTCCCTGACCCAGTTTCGCTCCTTTGTATTCAGTTGAATCAGGGGTGTCTTGTGACATCCTCCTTTGTTCTGTTTCCTGCCTTGGTTGCCTCATTAGTACATCTATGTTGATTGTTATTAGTGTGTATATATATCTAGGTTTATGTGTTTTAGCAGTCCAATGCCCTAACCATAACCCTCCACATTCACCGAGGACATTATTGTATTTTGCCAAGATCTACTTCCAGCCGGTGCAGAGTGATGGCTTCAGTCCCTGAGTGCCTGCCAATCATGGCTTTAGTCATGCCATCCAGGTTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40340
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 |
---|---|---|---|---|---|
ENSDART00000133855 | None | None | 107 | None | 5 |
ENSDART00000134357 | Nonsense | 89 | 975 | 2 | 7 |
ENSDART00000135345 | Nonsense | 250 | 527 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60971415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75452214 |
GRCz11 | 4 | 77028952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCTAGATGTCATCAGTCACTAGAGATGAAGATTGAATGTAAACATT[T/A]GTTTGAAGCAGCTGAACAAGACAAGCAGATCAGAACTGTCCTGACAAAAG
Long Flanking Sequence:
GACAGATTTTTGAAGAATGAACTTGAGAAGTTTAAGAAGATCTTACAAGAAGAAAACAGACAAGACTTTGTAAAGAACTTTAATGACAACAGATGCAGAATCACAGAAGCAGCTCTTGATCTCACACTCTTCTTCCTGAGAGATATGAAGCAAGATGAAGTTGCTGATACTCTCCAGGGTAAGATACTCATGACCGTCAGTTTGTCACTTACAAATATAGCTGGAAAAGTCAAGACTAAACCTATCTCTTTCTTTGCTCCTGTGTTTAGGTGAGCTGTTCTTCATTAACCAGTTAAAATGTAGCATGAAGAAGAAATATCAAAGTGTGTTTGAAGGAAATGCTCAGCAAGGAGACTCCACACTTCTGAATACCATCTACACAGATCTCTATATCACTCAGGGTGCGAGTGAACAGGTCAACACTGAACATGAGATCAGACAGATTGAAGTTGCTTCTAGATGTCATCAGTCACTAGAGATGAAGATTGAATGTAAACATT[T/A]GTTTGAAGCAGCTGAACAAGACAAGCAGATCAGAACTGTCCTGACAAAAGGAGTTGCTGGCATCGGGAAATCAGTCTCTGTGCAAAAGTTTGTTCTGGATTGGGCTGAAGGGAAAGAAAATCAAGACATCAGCTTCATATTTCCTCTTCCATTCAGAGAGATGAACTTAAAGGAGAAAGAAAGACAAAGTTTAAAAGACCTCATAACTCAGTTTTTCCCAGAGACTAAAGGACTGAACCTTACAAGAAGCACACGATTCAAAGTCCTGTTCATCCTTGATGGATTGGACGAATTTCGTCTTCCCCTAAACTTTGTTGGTAATGAGACGTGTCGTGATGTATCTTCAGCAGTCTCTCTGGATGTTCTCCTGACGAACCTCATCAAGGGAAATCTGCTTCCTTCTGCTCTCATCTGGATCACCAGCAGACCAGCAGCTGCCAGTAAGATTCCTGCTGACTGTATCGACCGGCTGACAGAGATACAAGGATTCAATGATGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38445
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 |
---|---|---|---|---|---|
ENSDART00000133855 | None | None | 107 | None | 5 |
ENSDART00000134357 | Essential Splice Site | 727 | 975 | 5 | 7 |
ENSDART00000135345 | None | None | 527 | None | 7 |
Genomic Location (Zv9):
Chromosome 4 (position 60980841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 75461640 |
GRCz11 | 4 | 77038378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATGTGTGATTGTCCAACAGTGTGATGTGGACTGTTTGTGTGTTTGTA[G/A]ATTGTCTGGCTGTATGGTGACAGAGGAAGGCTGTGGTTTGCTGTCTTCAG
Long Flanking Sequence:
TTCGTCAATTGGTGAAGGTTTGTTCTTTGCCACTGTTCATTGCTTAGTTTGGAACTTGTGGAGCTACGCATGCATGGATTGCTCTTCAGTGTTTGGACTTTCAGCAGTGAAAATTAAATTACACTGAACTGAACTAAACTGAACTTCAACTCTGAAAAGTAGACGGACACAGTTTAGATGGACTAGATCTTCTATGTTAAGCTGTGTTGACACAATCTACATGGTAACAATACTATATAAATAAAGATTAATTGAATTGAAATAGAAAACAAGATGTGACACACCCACAGTGGTGCTTTTTATGTGATGTATTATCAACAATATCTTTGTTTTTAGACCTTGTTGAGTATTTTAGTGAGTTTGCTGACCTCAGCGGTTGATCGATTGGGAAAAGTAATCAGCATATGTGTTTTCATCACTGGTGTTCGAATGAACCGAAACACCAGCATTTTCATGTGTGATTGTCCAACAGTGTGATGTGGACTGTTTGTGTGTTTGTA[G/A]ATTGTCTGGCTGTATGGTGACAGAGGAAGGCTGTGGTTTGCTGTCTTCAGCTCTGACTTCAAACCCCTCACACCTGAGAGAGCTGGATCTGAGCTACAATCATCCAGGAGATTCAGGAGTCAAGCTGCTCTCTGAACAACTGGAGGATCCAAACTACACACTGGACACACTCAAGTATGTAGAGCATCACTGCCCTTTTACACTTAATGGCTTTAAAAACAAATGTAAAAAACTTTATTGAAATTCCGTTTTCTGTGAGAATTGTGGGGTTTGGGCATTCATAATATATAGACTTAAAAGACATCTAGGGACTAAAGACACAATGTGATGAAGTGTTTGTTTTGTCCCCTTCTTCCCGCAAACAAATCTTAATGTGGGCAACAGTCCTTTTTAGCAATAATAGTGCCATCACAGAAGTGCAAGTATTTTTGCCAAAAGCACTGACACAACCTCATACCATGACAAACCCTGGCTTCTGGACTTGTTGCTGGTAACAGTCT
Associated Phenotype:
Not determined