ZMP
si:ch211-153a8.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
HAUS8
Human Description:
HAUS augmin-like complex, subunit 8 [Source:HGNC Symbol;Acc:30532]
Mouse Orthologue:
Haus8
Mouse Description:
4HAUS augmin-like complex, subunit 8 Gene [Source:MGI Symbol;Acc:MGI:1923728]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45791 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45791
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 |
---|---|---|---|---|---|
ENSDART00000125163 | Essential Splice Site | 168 | 357 | 7 | 10 |
ENSDART00000135785 | Essential Splice Site | 168 | 243 | 7 | 8 |
ENSDART00000143752 | Essential Splice Site | 168 | 267 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 12568487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 12527289 |
GRCz11 | 23 | 12462259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTCATATTTAAAGCTGTCAGTTGTTCATGTTTTTTGTTTCATTGTCTA[G/A]ATGGAGCATAGTAACCGGAAACTGAGAGAGGAGGCAGAGAAGAATATTCT
Long Flanking Sequence:
ACATAAAAAACATATAATTTTTATTCGGAAACAAAGCTTTTTTTTGCACTGCAACTAATCATCAACGAAAAAAGTTTTTAACCTTTTTCACAACCAGAAAACCACCAATCTAGAATGAATGATTATATGGTGTCATGGCTGTGCAATCAAAAAATGTCATTATAATGGATTTCAATGGGGCAAAAACAGCCACCAACATAACGAAAGAGTAGTAAATTTACCCAGAGTGTATTGTTGAATTATTGAAAAAATAATTTTCCCAAAATATGTGTCAAAATCAGGTTTGTCACCAAAAATCATTTAATTTGCTGAAACAGAAAGTTGTGACCAAATTAAGACTCAAAATCATCCCAGAGTGGATGAAAACATCCTTAACAGCAGACAAGGATTGAGATGTTAAGTTTGTTCGTTTCAGTGTGTTTCCGTCCTAGTACTATATTTTGTGCTGAAAATTCATATTTAAAGCTGTCAGTTGTTCATGTTTTTTGTTTCATTGTCTA[G/A]ATGGAGCATAGTAACCGGAAACTGAGAGAGGAGGCAGAGAAGAATATTCTGACCGTGATGCAGAAAGAGCAGCAGCAACACACAGAAGTAAACCCCAAGAAGCGTCAGTATCTGCTGCTGCAAAAGCAGAAAGAGCTCAACAGTTTACTGGACTTACAGGTCATTTTCAAATATTTAACATGTTCTTAAAGGAATAGTTCACCCAAGAATATAAATGTATCCTGGCTCTTCAATAATTTTGTCGGTGGTACAGAATGTCCGCAGGGTCTTAAAAAGTGTTAAAAATTGATGAATCAATTGAGAGAACTTTAAGGCACTTAAAAAGTTTCAAAAAGTCTCAAATGCTTTTTTACAAGGTATTACATTTTATATCAGTATGCTAAAGTTGACTGAATTTAATCTGCGACTATTAAGATGTTGTGTAGTTTATGAAATCAAAAAATCCTGCTGGATTTGACATCACACTGCTTTGTTTACTGTAAACAAGGCAACACTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30736
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 |
---|---|---|---|---|---|
ENSDART00000125163 | Nonsense | 208 | 357 | 7 | 10 |
ENSDART00000135785 | None | None | 243 | None | 8 |
ENSDART00000143752 | Nonsense | 208 | 267 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 23 (position 12568608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 12527410 |
GRCz11 | 23 | 12462380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCAACACACAGAAGTAAACCCCAAGAAGCGTCAGTATCTGCTGCTG[C/T]AAAAGCAGAAAGAGCTCAACAGTTTACTGGACTTACAGGTCATTTTCAAA
Long Flanking Sequence:
ATTATATGGTGTCATGGCTGTGCAATCAAAAAATGTCATTATAATGGATTTCAATGGGGCAAAAACAGCCACCAACATAACGAAAGAGTAGTAAATTTACCCAGAGTGTATTGTTGAATTATTGAAAAAATAATTTTCCCAAAATATGTGTCAAAATCAGGTTTGTCACCAAAAATCATTTAATTTGCTGAAACAGAAAGTTGTGACCAAATTAAGACTCAAAATCATCCCAGAGTGGATGAAAACATCCTTAACAGCAGACAAGGATTGAGATGTTAAGTTTGTTCGTTTCAGTGTGTTTCCGTCCTAGTACTATATTTTGTGCTGAAAATTCATATTTAAAGCTGTCAGTTGTTCATGTTTTTTGTTTCATTGTCTAGATGGAGCATAGTAACCGGAAACTGAGAGAGGAGGCAGAGAAGAATATTCTGACCGTGATGCAGAAAGAGCAGCAGCAACACACAGAAGTAAACCCCAAGAAGCGTCAGTATCTGCTGCTG[C/T]AAAAGCAGAAAGAGCTCAACAGTTTACTGGACTTACAGGTCATTTTCAAATATTTAACATGTTCTTAAAGGAATAGTTCACCCAAGAATATAAATGTATCCTGGCTCTTCAATAATTTTGTCGGTGGTACAGAATGTCCGCAGGGTCTTAAAAAGTGTTAAAAATTGATGAATCAATTGAGAGAACTTTAAGGCACTTAAAAAGTTTCAAAAAGTCTCAAATGCTTTTTTACAAGGTATTACATTTTATATCAGTATGCTAAAGTTGACTGAATTTAATCTGCGACTATTAAGATGTTGTGTAGTTTATGAAATCAAAAAATCCTGCTGGATTTGACATCACACTGCTTTGTTTACTGTAAACAAGGCAACACTTTTATTCCTGCTGTTGTAGGCACGACCTCCTGTATTAGCATTTTTATTCATTTAATTGTTCATTTATTTATTTTCTACCGCTTTTCCGGGGCCGGGTCGCGGGGGCAGCAGTCTTAGTAGAGAACC
Associated Phenotype:
Not determined