ZMP
sass6
Ensembl ID:
ZFIN ID:
Description:
Spindle assembly abnormal protein 6 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q7ZVT3]
Human Orthologue:
SASS6
Human Description:
spindle assembly 6 homolog (C. elegans) [Source:HGNC Symbol;Acc:25403]
Mouse Orthologue:
Sass6
Mouse Description:
spindle assembly 6 homolog (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1920026]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43780 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5967 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45755 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43780
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 |
---|---|---|---|---|---|
ENSDART00000081191 | Nonsense | 354 | 627 | 9 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 10854980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10715148 |
GRCz11 | 22 | 10744830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAAGACCAGCTTGTGCTGAGGACCAAAGAAGTGCTGGAGGCCACGCAG[C/T]AGCAGAAGGTTAGAGAGCTTTGTGTGTGTGTGTGTGTGTGTGTATTGGTA
Long Flanking Sequence:
GGTTGAATTCAGGCCCATTCTGTCACTGTCTAATTTGAATACAGAATCGATTCTGAATATTACAAAACAAGAGTCTTCAAAATCGAGGACATTATGCTTGCATCATTTTCAAAGACTTGTTTTCGGGTGTTTACATGGACATGACAATGGCAGCATTTTCAAAACTTTGCACTTTAAAATTCGTTTTCTCACAAAAATGCTTTTGGCATGTAAACAAACGGGCAAAATTCACAAAAAGTTTGAAAACGTTGGTTGTAAAGGATGTCCTTTAAATGGCCTAAAATGGAGTTTTGTTTGTGCGCACCTCCGTCCAGGAGTGTCAGCGGTCCAAGCAGCAGGTGTTGTCGTTGAGGAGGGAGAACAGCGCTCTGGACAGCGAGTGTCATGAGAAGGAGCGTCTGCTGAATCAGCTGCAGACACGAGTGGCCGTTCTGGAGCAGGAGATCAAAGATAAAGACCAGCTTGTGCTGAGGACCAAAGAAGTGCTGGAGGCCACGCAG[C/T]AGCAGAAGGTTAGAGAGCTTTGTGTGTGTGTGTGTGTGTGTGTATTGGTAAATTATACACAAAAAAGGCTGTTTAAGACGATTTTTAAAGAGTAAATCTTTATTGAAATTTCTTTTGGTTGAAAGGTAAAATATTGCCTGACTGGCAACATACCTTTCGGTTTTGGGAGAGAGCGGCTTGATTGTTAAAACACGAGATGCAAACAGTTGGTGGAAGAAGAAAAAAAAACTGTAAACACTCTTGTAGGCCTATTAATTAATAATTTTTTTAACATTGAGTGCACTGATGAGGTGCAAATAAGAAAGGCTTAACATCAGACAAAGTGATCACTGCAGGTTCCATGATTTCTGTGGTTGCTTTTGTTTCTCTGCAGTTTTGGATTGTCAGGATTGTCAGTAGTGCAGTATTGCTAAATCTCCTTTTGTTTTAATCAGAAAATATGAACATTAAATAAGATTACACTGATTTTACTAGGGATTTAGTAGTAGGGCTGCTAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5967
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 |
---|---|---|---|---|---|
ENSDART00000081191 | Essential Splice Site | 356 | 627 | 9 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 10854971)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10715139 |
GRCz11 | 22 | 10744821 |
KASP Assay ID:
554-3839.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTTGTGCTGAGGACCAAAGAAGTGCTGGAGGCCACGCAGCAGCAGAAG[G/A]TTAGAGAGCTTTGTGTGTGTGTGTGTGTGTGTGTATTGGTAAATTATACA
Long Flanking Sequence:
CAGGCCCATTCTGTCACTGTCTAATTTGAATACAGAATCGATTCTGAATATTACAAAACAAGAGTCTTCAAAATCGAGGACATTATGCTTGCATCATTTTCAAAGACTTGTTTTCGGGTGTTTACATGGACATGACAATGGCAGCATTTTCAAAACTTTGCACTTTAAAATTCGTTTTCTCACAAAAATGCTTTTGGCATGTAAACAAACGGGCAAAATTCACAAAAAGTTTGAAAACGTTGGTTGTAAAGGATGTCCTTTAAATGGCCTAAAATGGAGTTTTGTTTGTGCGCACCTCCGTCCAGGAGTGTCAGCGGTCCAAGCAGCAGGTGTTGTCGTTGAGGAGGGAGAACAGCGCTCTGGACAGCGAGTGTCATGAGAAGGAGCGTCTGCTGAATCAGCTGCAGACACGAGTGGCCGTTCTGGAGCAGGAGATCAAAGATAAAGACCAGCTTGTGCTGAGGACCAAAGAAGTGCTGGAGGCCACGCAGCAGCAGAAG[G/A]TTAGAGAGCTTTGTGTGTGTGTGTGTGTGTGTGTATTGGTAAATTATACACAAAAAAGGCTGTTTAAGACGATTTTTAAAGAGTAAATCTTTATTGAAATTTCTTTTGGTTGAAAGGTAAAATATTGCCTGACTGGCAACATACCTTTCGGTTTTGGGAGAGAGCGGCTTGATTGTTAAAACACGAGATGCAAACAGTTGGTGGAAGAAGAAAAAAAAACTGTAAACACTCTTGTAGGCCTATTAATTAATAATTTTTTTAACATTGAGTGCACTGATGAGGTGCAAATAAGAAAGGCTTAACATCAGACAAAGTGATCACTGCAGGTTCCATGATTTCTGTGGTTGCTTTTGTTTCTCTGCAGTTTTGGATTGTCAGGATTGTCAGTAGTGCAGTATTGCTAAATCTCCTTTTGTTTTAATCAGAAAATATGAACATTAAATAAGATTACACTGATTTTACTAGGGATTTAGTAGTAGGGCTGCTAGCATAGACATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45755
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 |
---|---|---|---|---|---|
ENSDART00000081191 | Nonsense | 477 | 627 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 22 (position 10851058)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10711226 |
GRCz11 | 22 | 10740908 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTTTCTCATGTGTATTTTCTGTTTTTCTGTCCCTCAGTAATAACGTG[G/A]CTGAACAAGCAGCTGAATGAGAATCAGCTCTCCAGAAAGCAGGAAACTGT
Long Flanking Sequence:
AAATTGTTTATTCAAATGATATTTATTGTTTTTTTGTTTTTATGCATTTTAAATGTAATAGTTTGTTTCATTTTAACATTTTTCTCAAAGCTGTAAGTTTTGTCTTTGTTTTATGTTCTTTAATAATTTATTATTATTTTTCATTTAGAGTATCATTTAGTACTATTTTATTTAGAATTTAATGTATTCCTCTATTGATAATTCTATTACTTTTGTTTTTAATTTTATGAAATGAAAGAGAATTCATTTCAACACAACTGATTATAAATATTCAAATAAAAATTTATATTAAGGCAATTTACTGTCTTTGTTTATTTTTATTAAAATCCATTCGATTATTTGTATTTTTATTTATTTTGTTTGTTTTTTTACAGTTATTACGTTTAGAAGAAATGAGATTTTGTGTTAGTGCAATATAACTTATCATAAATGATTTCATTAGAGCGTTGTGGTTTTTCTCATGTGTATTTTCTGTTTTTCTGTCCCTCAGTAATAACGTG[G/A]CTGAACAAGCAGCTGAATGAGAATCAGCTCTCCAGAAAGCAGGAAACTGTAGCCATGTTTGAGACGCCTGCAGCGGCACTGAGATCAGCCGCTGTCCCGCACAATATGGTGACCAATCACACAACACACACGCACCAAATCCAGCAGACTGTAAATCATGCCTTCAGCTGTAGTTTGATGATCTGCATGTGTGAGTGATGTAGTCCTCCTCCTGTTCTCCAGCTTGATAGTAAAGGTTTGTTGTCGTCTTTGGGACAGGCTTTCCCCATCACCTCTACCATAAACTCCAAATATCCTCTTGCCCTGTCATGTGTGAGCTCAGGATCTCGATCTGTCCTGACCAGCAGCAATGGACCCAAGGCAGGCCTTTCTTCTATTTCTCTTTCTGTTTCTCCTGTGTTTCTCCTGGTTCTGTGGTTTGAGTGTTTCAAGCTCTTTACATGACAACAATGTAGCCAAAAACAACTTTTTTTTTTCAATTTGCCTTTTGAAAAAGTTTT
Associated Phenotype:
Not determined