ZMP
zgc:92661
Ensembl ID:
ZFIN ID:
Description:
HAUS augmin-like complex subunit 4 [Source:RefSeq peptide;Acc:NP_001002425]
Human Orthologue:
HAUS4
Human Description:
HAUS augmin-like complex, subunit 4 [Source:HGNC Symbol;Acc:20163]
Mouse Orthologue:
Haus4
Mouse Description:
HAUS augmin-like complex, subunit 4 Gene [Source:MGI Symbol;Acc:MGI:1261794]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40347 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14302 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40347
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022132 | Splice Site, Nonsense | 159 | 367 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 1818173)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 1444523 |
| GRCz11 | 5 | 1498963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTCTGGGATTGACTGCAGAGCGAGTGAAGAGACTGATGCCTTCTGAA[C/T]AGGTGCTACATTACTCACTCAGTGTTTGAGGACAAGTGCATTGAAATAAA
Long Flanking Sequence:
CAGGCGGAGCGAGAGTTGCACACTCAGAGGTTGAGTTGGCTGCGTGTGGAGAGCATACATCGGCTGCTGAGAGAGATCATCCAGGAGAACCACTTCAGTAAAGCCTCCAGCGCTCAGACAGGAGATGCCACGGTACCACATGTATATTAATATAGAGATATCACACTCTTATTTACCCATTTCAGCACAGACTTGTACTGTAATAGCATGGTAGAGGCACTTGTTGTGAGATGGCATTTTCATTTGTTTGGATGTCCTATTCAATAAACCCAGATCACACAGTATTTTTAATTATGTTTAGCCAAATCAATGTCAGACTTACATTAGTATACTTAACAATGTTATAATGTCTTCTGGGGCAGTTCTACAGCACACTGGAGCAGTGTTTGATGGTGGGTCAGTGTGTGAAACGGATGGACATCAGCGCTGACGTCAGTGAACCTCACAGCGGCATTCTGGGATTGACTGCAGAGCGAGTGAAGAGACTGATGCCTTCTGAA[C/T]AGGTGCTACATTACTCACTCAGTGTTTGAGGACAAGTGCATTGAAATAAATGCAATTTATCAGATTTAGGACTCTTATTATCACTTATTTCTAATCCCACGTAAATAATAAACAAATGTGAGTGTGCAAGCTAACATGTAACGTGGCACGCATTAAAGAGTCATTGACATTATTTGATGCACAACAAAAATGGTACTTCTGTTCTTGTGCCTTGAGCTGCTACAGTTATAGTAAATTACCACTAGGTGGCGCTCCAGCCGAGCACACAGGAACTGCAGATCAAACAGGATTGAGTTGTGAGTATCATTGTCACCTAGGCTGCATCCCGGTACAGTTTTTATGCCCTTTACTCTGTCTCGTTCATTTAGATCATGGGAGCCCAAACGTTTTTATGAAGGGTCAAAAACTAAACTTGATTGAGGCTAGTGGGCTGGTGGTAAATATTGCCATGGATGATTGGCTAATTTATTTAATAAAATTTAAAGATAACTAGAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14302
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022132 | Essential Splice Site | 240 | 367 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 1821923)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 1448273 |
| GRCz11 | 5 | 1502713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CMGAGAGAAYRCCACGCTACTGCMGCGGCAGACACACACGTACCTGTCTG[T/G]GAGTCCAGAGACACTCAKTAGCCGCATTTCCRYTATCGGGCCAGTGCRAG
Long Flanking Sequence:
GGAACGCTAGCCCAGATAGATATGCAGCGTGAAAACATCAATAGTTTAAAATCCTGTAGTCTGAACTCAAATTTAAAAACGGCATTGAAATAAAAACATCAGAAGTGTGTACAAGGCTTTACTTTATAAAAGGGACTCATGATGACATGTTGTTTTTTGCAGGACGTCCTGCAGATGAAGCAGAAGTGTCCGTCAGAGCTCCTGCAGCACCTGAAGAAGAAAAGCGTCGCCATCCTGACATACTACCAGCCTGACTGGGGTGAGCTGAGCCACGCTGCTGAAAGAGCTTTGTTTTAAAGGGACGGCTGTTTTTATTTAGATGTGGCACTTAAGTATTTTCTCGTCTCTCTTAGAGAATGAAAGCGAGGGTCTGAGGAGCGTCAAGCTTTCTAAACTTCCCGAACTGCTGGATGGGGAAAAGAAGAAAGTGAAGAGTCTGACTGAGAAAAACCGAGAGAATACCACGCTACTGCAGCGGCAGACACACACGTACCTGTCTG[T/G]GAGTCCAGAGACACTCATTAGCCGCATTTCCGTTATCGGGCCAGTGCGAGCCATGGCTTTAATCGGGCTGGGCCAATCGCCCGGGAGGTTGAGAAATGAGGCTGAAATCATGTCGCGTTTCCACTGTCAGGCTAGTAGCTTACAGCGCGTCACGCAAACACCGCCCACAGAACATCCCCGAATCAAACGTCACACAACCCGCCCACTTCAGCGGGAATCAGGCAGATAAAGCACACCATAGAATCATCACGAAACGAAACCATTAAAATGAAGACAACCGAAACAAACAAATGACCCGTTACTGTACATCAGTACATGAAATGTCTATACCTGTGTATTTCCATTCATTACATTTGTTTACTCGCCGACCGACTGTTGGCATTGTGCATCGAGTGCTCTCGCCACTAACGGAGTGACCCAACACAGAGAACGCACACATCCATAATATAAAGCCACAGAAATTCTCCTTTATAACTCGATATGGCATGTATTTTATAACA
Associated Phenotype:
Not determined