ZMP
si:ch211-258l4.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebratesirtuin (Silent mating type information regulation 2 homolog) 7 (
Human Orthologue:
SIRT7
Human Description:
sirtuin 7 [Source:HGNC Symbol;Acc:14935]
Mouse Orthologue:
Sirt7
Mouse Description:
sirtuin 7 (silent mating type information regulation 2, homolog) 7 (S. cerevisiae) Gene [Source:MGI
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24226 | Nonsense | Available for shipment | Available now |
| sa30735 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24226
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085685 | Nonsense | 109 | 405 | 3 | 10 |
| ENSDART00000130055 | Nonsense | 102 | 376 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 41984391)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38952384 |
| GRCz11 | 22 | 38939129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAGCAGCTGGCAGAGGCAGTCCAGCGGGCCAAACATCTGGTCATTTA[C/A]ACCGGAGCAGGAATCAGTACGGTGCGTCTCGCGTTCAGCTCAAAGCTTTT
Long Flanking Sequence:
ATTTTTATTTGTTTTCCAAATATTTCCCTTATGCTGAGTTAAACAGACAGAAGGCATTTTCACAGTATGTCTATGTTTTTTCTTCCAGAGAAAGTCGTCTTTATTTTAGTCTGACTGGAATAAAAGCTGTGATATATTTATTTTAAATATATTTTTATTCTAAATATATATATATTTATCTTTTTACAATGTTTAAGGCCAATATTATTAGTCATCCTAAGAAATGTATGATGTTTTCAATTATCTACACAACAGAACACTGGCATCTAATAACTCGACTAATTATTCCAACAAGTTAACATAATAACCTAGTGAAGTCTTTATATTGCGCTTTAAACTCATTACTAATATCTTGAAAAATAGGTACAAGCATTTACATTTGACAGGAGTACACTAATCATTTTGGGATGTTTGCAGGTGTTTGATGATGCTGAGAACTTGAAGACTAAAGTGAAGCAGCTGGCAGAGGCAGTCCAGCGGGCCAAACATCTGGTCATTTA[C/A]ACCGGAGCAGGAATCAGTACGGTGCGTCTCGCGTTCAGCTCAAAGCTTTTTAGATGGATTGTAATGTGCTGAAGAACATCCTTTCAAAACTTACTCACTATTAGTATTTACTCACCCTCAGGGTGTTCCAAACCTGTGTGAGTGTCAATTTTCCTCTGTTGATTCCAAAAGAGGATAGGTTGGTATCCAGATACGGCACTCGGGACCTGTGTTCAATAGCAGACGATTGTCTATGCTAGATTTCAATGGCAGACAGTGATCTAGGCTATTTTTAACAGCAGATGTATAACATAATAAATAGCTCTGATAAATAGTTTATTGACAATTCAGTATGCAATCCCAAAATGTTATTTTACAAACCCCCTGGGTTACATCTCAAATGAGAAAGAAAGAATAATTTGGAGGTCAAAATGAGCATTTGATAGCCATGCAGCACTATAATTATTAAATGCTTATGGAACAGCAGGTCTATGTCTGTGTTGGTCCTGTTGAATACGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30735
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 |
|---|---|---|---|---|---|
| ENSDART00000085685 | Nonsense | 356 | 405 | 10 | 10 |
| ENSDART00000130055 | Nonsense | 327 | 376 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 41990605)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38958598 |
| GRCz11 | 22 | 38945343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGCAGGACCCCATCTTCAGCATGGCTAAACCCCTCAGTCCGCAAGAG[C/T]AGAAGAGTCACTCTCGTAAAGAGATAGCGCCACCTTCTGCTTTAGAGGAG
Long Flanking Sequence:
ATTTACTGTCATCATGACAAAGAGGAAATAAATCAGTTATTAGAGATGAGTTATTAACACTGTTATGTGCAGACATGTGCTGGAGAAACATCTGAGAAATTGGGGAAAGAAATAACAATTCAAAGGGGGGCGAATACTTCTGACGTCAACTGTATGTGTAAATATATATATATATGTGTATATATATATATATATATATATATATATATATATATATATATATATATTGAGAACCAGAATTTGACAGTAGGTCTAATAATTCTGCCTTCCACTGATGGTGTTTTACACTAACTTGGCTTTTTTCTAAGAATGTATAGGTTTTGGTTTGAGCTGCTTAAGCCCCAGTGATGGTCATGTTTAAAGAAAAGGCTGTTAATATTAGATTAATTTGTAGGTCTTCAAATGTTTACTCGTTTGATTAATATTGCCTGTGTTTTATTCTTAATTACAGATTGCAGGACCCCATCTTCAGCATGGCTAAACCCCTCAGTCCGCAAGAG[C/T]AGAAGAGTCACTCTCGTAAAGAGATAGCGCCACCTTCTGCTTTAGAGGAGGTTTCGCAGTCAGCACCGCCACAGGGTGAAGGGCCAGCGGTTCAGGGCGGCTGGTTTGGAAGAGGTTACTCCAAAGGAAGACGGAAAAAGAAGAGTTCCTAGAGTTCATGTTAGGTATACGTCACCCACACAGCTGCTCAAACACACACTTTAGCTTGGTTTAGACTTGTGTTCAGGGTGCGTCACGTTTACAGGTTAAAAAAAAACCTATTGATAACTGGTTTTCTGAAGGGTTTTTTAAACCACTGGTAGAAGAGTAAAACCTCTGCAGTGGAAAAATCAAAGGCTTACACTGAAAAATAAGCTTTTCTTATGAGTTTTTATCTTGTTTCTTGCACAAATATCCAACAATTCTGAAATCAAGAAGAATCTTCACGATGAGTGAAACATGTCGTCTTATTTTCAGAAATATTTCAATTGACTTTTCCCTTAAAACAAGGTATAATATAA
Associated Phenotype:
Not determined