ZMP
si:dkey-103i16.6
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557125 [Source:RefSeq peptide;Acc:NP_001038173]
Human Orthologue:
SIRT3
Human Description:
sirtuin 3 [Source:HGNC Symbol;Acc:14931]
Mouse Orthologue:
Sirt3
Mouse Description:
sirtuin 3 (silent mating type information regulation 2, homolog) 3 (S. cerevisiae) Gene [Source:MGI
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23259 | Nonsense | Available for shipment | Available now |
sa36601 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23260 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23259
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099777 | Nonsense | 93 | 370 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 14871210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15316628 |
GRCz11 | 18 | 15285140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGCGGGGCTTTGGAAACCATCGGCAGGCTGATGAAGCTTGGTCGAGTG[C/T]GAAACATTGTGGTAGTTGCTGGAGCAGGAATCAGCACAGCCAGCGGGATC
Long Flanking Sequence:
AAGAAAAACAAAATAAGCAGCTCAGCTATCAGAACATAGTAGACATAGTAAGTGTATTTATACACACAAACACTAAAATCTGCTGTTTTACTCCACATAACTCCATATAAAAGCCAGAAACTTTTTTGCACAGGTTTGTCTAAAGGGTTAATTATGCCAACTGATGACCAACAGTAAAAATTGCACAATTGTTTCCTCTTCCCAACAGGAAAACCACCAACAATCAACAATGCATGATTATGCTGTCATGGCGATCAAAAATGTAATAATAATGGGAGTCAATAGGGCAAAAACAGCCAAGAACATAACAAAAGGGTGGTTAATTTGAACAGTACACAAGGGTTAAAAAGTGGCATATAATAGAGCCTAAGTTCTGTGTTGTATTTCTGCATCTCTTCAGGAAAGGTAGTAGTAAGCCTGCTCTGTCCTCACCCTCTGGACGCTCAGTATCGCGCGGGGCTTTGGAAACCATCGGCAGGCTGATGAAGCTTGGTCGAGTG[C/T]GAAACATTGTGGTAGTTGCTGGAGCAGGAATCAGCACAGCCAGCGGGATCCCAGACTTCAGGTGAACACACACACAAAACCACAAACCTTCAGACTGCTGCTAAAATCTCATGACCCTCAACTAACACTTCTCTCTCTATATCAGGACTCCAGGAACGGGTCTCTACGCAAACCTAGCAAAGTACGACATCCCTTACCCAGAGGCCGTCTTTAACATCGACTACTTTTCTGACAACCCTCATCCCTTCTTCTCACTGGCTAAAGAGCTTTATCCTGGACACCACCGGCCCAACTACGTCCACTACTTCATCCGCATGCTGCATCAGAAAGGCCTGCTGCTCCGCATGTACACCCAGAACATCGACGGTCTCGAAAAACGTGAGCTTAAATGGACAGTTCAGATAAAAATAAAATAATTGTCGTTTACTCGCCTTTTTTAGTTTCAAACCATTGAGTTTTTCTTGTGTTGAACACAAAAAGATGCTAACTATAAAACTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36601
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 |
---|---|---|---|---|---|
ENSDART00000099777 | Essential Splice Site | 113 | 370 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 14871273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15316691 |
GRCz11 | 18 | 15285203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTTGCTGGAGCAGGAATCAGCACAGCCAGCGGGATCCCAGACTTCAGG[T/C]GAACACACACACAAAACCACAAACCTTCAGACTGCTGCTAAAATCTCATG
Long Flanking Sequence:
ACACAAACACTAAAATCTGCTGTTTTACTCCACATAACTCCATATAAAAGCCAGAAACTTTTTTGCACAGGTTTGTCTAAAGGGTTAATTATGCCAACTGATGACCAACAGTAAAAATTGCACAATTGTTTCCTCTTCCCAACAGGAAAACCACCAACAATCAACAATGCATGATTATGCTGTCATGGCGATCAAAAATGTAATAATAATGGGAGTCAATAGGGCAAAAACAGCCAAGAACATAACAAAAGGGTGGTTAATTTGAACAGTACACAAGGGTTAAAAAGTGGCATATAATAGAGCCTAAGTTCTGTGTTGTATTTCTGCATCTCTTCAGGAAAGGTAGTAGTAAGCCTGCTCTGTCCTCACCCTCTGGACGCTCAGTATCGCGCGGGGCTTTGGAAACCATCGGCAGGCTGATGAAGCTTGGTCGAGTGCGAAACATTGTGGTAGTTGCTGGAGCAGGAATCAGCACAGCCAGCGGGATCCCAGACTTCAGG[T/C]GAACACACACACAAAACCACAAACCTTCAGACTGCTGCTAAAATCTCATGACCCTCAACTAACACTTCTCTCTCTATATCAGGACTCCAGGAACGGGTCTCTACGCAAACCTAGCAAAGTACGACATCCCTTACCCAGAGGCCGTCTTTAACATCGACTACTTTTCTGACAACCCTCATCCCTTCTTCTCACTGGCTAAAGAGCTTTATCCTGGACACCACCGGCCCAACTACGTCCACTACTTCATCCGCATGCTGCATCAGAAAGGCCTGCTGCTCCGCATGTACACCCAGAACATCGACGGTCTCGAAAAACGTGAGCTTAAATGGACAGTTCAGATAAAAATAAAATAATTGTCGTTTACTCGCCTTTTTTAGTTTCAAACCATTGAGTTTTTCTTGTGTTGAACACAAAAAGATGCTAACTATAAAACTGCTAACTATTGATTTTCATTTAATTTAAGGATGCTCATAATAAACAATTACCCGTTGACTGAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23260
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099777 | Essential Splice Site | 190 | 370 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 14871589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 15317007 |
GRCz11 | 18 | 15285519 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCTGCTGCTCCGCATGTACACCCAGAACATCGACGGTCTCGAAAAAC[G/T]TGAGCTTAAATGGACAGTTCAGATAAAAATAAAATAATTGTCGTTTACTC
Long Flanking Sequence:
TGTATTTCTGCATCTCTTCAGGAAAGGTAGTAGTAAGCCTGCTCTGTCCTCACCCTCTGGACGCTCAGTATCGCGCGGGGCTTTGGAAACCATCGGCAGGCTGATGAAGCTTGGTCGAGTGCGAAACATTGTGGTAGTTGCTGGAGCAGGAATCAGCACAGCCAGCGGGATCCCAGACTTCAGGTGAACACACACACAAAACCACAAACCTTCAGACTGCTGCTAAAATCTCATGACCCTCAACTAACACTTCTCTCTCTATATCAGGACTCCAGGAACGGGTCTCTACGCAAACCTAGCAAAGTACGACATCCCTTACCCAGAGGCCGTCTTTAACATCGACTACTTTTCTGACAACCCTCATCCCTTCTTCTCACTGGCTAAAGAGCTTTATCCTGGACACCACCGGCCCAACTACGTCCACTACTTCATCCGCATGCTGCATCAGAAAGGCCTGCTGCTCCGCATGTACACCCAGAACATCGACGGTCTCGAAAAAC[G/T]TGAGCTTAAATGGACAGTTCAGATAAAAATAAAATAATTGTCGTTTACTCGCCTTTTTTAGTTTCAAACCATTGAGTTTTTCTTGTGTTGAACACAAAAAGATGCTAACTATAAAACTGCTAACTATTGATTTTCATTTAATTTAAGGATGCTCATAATAAACAATTACCCGTTGACTGAAAGAGTGCGTTTTTAACTGGTTAATGGTATCAGTTAAATGATTAAAAGTTCGGCTGCATAAATGTGCAACACAGATTTGTTAACTCGTGGGATGGTAACACTTGCAACCACATGTGCCTACAGATGTATTTTGGCAAAGACGGAAAATAAAAGAAGAATGTTGCTGGTCACAGTTTGACAGATGAGTTGATTTCAAACCAGCGCTGATGCTCAATGCCTCTGTCCTGGAGCTGCCTCTTAAACACTACCATTTATTTGCCGAATTGGAGAAAGAAGCGCAAAATAAAACTTTCTGAAATGTGCTCTGCTTTGAAAACATT
Associated Phenotype:
Not determined