Busch Lab

ZMP

haus6

Ensembl ID:
ENSDARG00000068210
ZFIN ID:
ZDB-GENE-030131-5517
Description:
HAUS augmin-like complex subunit 6 [Source:UniProtKB/Swiss-Prot;Acc:A0JMF7]
Human Orthologue:
HAUS6
Human Description:
HAUS augmin-like complex, subunit 6 [Source:HGNC Symbol;Acc:25948]
Mouse Orthologue:
Haus6
Mouse Description:
HAUS augmin-like complex, subunit 6 Gene [Source:MGI Symbol;Acc:MGI:1923389]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa41065 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34221 Nonsense Mutation detected in F1 DNA Not yet available
sa21120 Nonsense Available for shipment Available now
sa5451 Essential Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa41065
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098503 Essential Splice Site 39 794 1 16
ENSDART00000133410 None None 289 None 7

The following transcripts of ENSDARG00000068210 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 65681040)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58862780
GRCz11 7 59165210
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGATAACGTTTCCGTCACCAAAACAACGAAACATCTGAATCTGGGAATG[T/G]AAGTCTTATCTTTATTTTCTTCACATCCGAATAGCTTCTATGTTAGCCCG
Long Flanking Sequence:
GCCCATCTTCAGTGGTCGCGTCCCAATACATCCTCGTATTACACGCACTTAAGTGCTAAATGATGGCTTCGCTATTTCACTTTAGCCTACTATGCGTAGATGTGGATCAGGACTGGACGAGGGCATAAGCTTGTCGTGACACATTTTAGACAGACTCACGGAAACTCTAAACACGCTCAAATAATTTGGCGGTTAGAAGGAAGTTGCTGTGCCCACACATTGTAAATATTTTAACAAGTCACGTTAGGCTTAAGTTAATTTATAGCTCGCATACAGGTCAAATCTAATTTCGAACACTATGCTTTGAATGGGTTATAGAGTTATCTGTTGCTCAATCTTGACGCTTTTAACGTTAGCCTGCTAACGTTACTGTGTTTAGCGAAATGTCTAAACTTAAGAAAACAGATGGTAAATACCTGTGGTGGTGTCTCTTGTGCCTCAAATTCAAACCGGATAACGTTTCCGTCACCAAAACAACGAAACATCTGAATCTGGGAATG[T/G]AAGTCTTATCTTTATTTTCTTCACATCCGAATAGCTTCTATGTTAGCCCGTGTTATCCAGAATGTAGTTTAGTTCTTGTGACTATTATGTATAATTGACCTAATTAATCTTAGTTTTCTTTAATTTTATCAGCAGGACTTTTAACTTCGGTAAAAGGTTGTTTATAGATCTTTAATATTTCTTGAGTTACAGCCACAAACATTGATTATAATTTTTCCATCACTTAACGTTAGTGTGATCTATGTAAATATTTTAATAGAATAAACGAGATATATCTCTAGTTTCAACATAATTTGTTGTTCAGACATTTCTCTTTAACGTTAGTAGGAAAAAATATATTAACAACTATATGCAAGTTGCCCTTCATTTGGTTTTTGAAGGGTACAATTTGACAGTTTATTCGTGGGGCCATATTGACAAAGACATACCGATAGAAATAGAAAAGATAAGGCTCTAAAGTTGTATGCAAAAAAGGACATGTTTGTTTAGAAACAGAATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34221
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098503 Nonsense 48 794 2 16
ENSDART00000133410 None None 289 None 7

The following transcripts of ENSDARG00000068210 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 65680278)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58862018
GRCz11 7 59164448
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCATGTTATTATATTTTTTTATAGGAACATGTTTGACAAACCAAACAAA[G/T]AGGCATTCTACATTGTCATTCACTTTTTATTTAATAAACTGAATCCCACT
Long Flanking Sequence:
TAAACGAGATATATCTCTAGTTTCAACATAATTTGTTGTTCAGACATTTCTCTTTAACGTTAGTAGGAAAAAATATATTAACAACTATATGCAAGTTGCCCTTCATTTGGTTTTTGAAGGGTACAATTTGACAGTTTATTCGTGGGGCCATATTGACAAAGACATACCGATAGAAATAGAAAAGATAAGGCTCTAAAGTTGTATGCAAAAAAGGACATGTTTGTTTAGAAACAGAATTCAAAAGGAAATTGAGATATTTTAATGCATCAGAGTATGACTTCAAAACAACATTTGCAAAGAAGAACATTTTTCTCAAATTATATCAAGAAGTTTAATGTTTGAATAAAACCAAAATTTTTGTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTGTAAATAAAACTATATGCATGTTATTATATTTTTTTATAGGAACATGTTTGACAAACCAAACAAA[G/T]AGGCATTCTACATTGTCATTCACTTTTTATTTAATAAACTGAATCCCACTCGTGCCCAAGACGTCTTCAGGTAGAACTATATAGTCATATTTAAATGTTTCCTTCTTATTCTGTTGTAATTTGACATTCCAAATTTAAAAATATTTTTGTTTGCTTAGAAATTGCTGGCTAGTTTGGGATCATAAAAGTGATGCTGAGTTTCGCAAGGTGGCTTTTGCATGGCTCCAGGAGATAGCGGTATGTGGTGTTTTATATACAATATTCTGTTACTAGTCTGCCTGTTGCATTGCTAGAGAATCTTTACAGACAAACTGTATTATTAATATAACTGATATAATGTTACAGTTATAGGATTGTATAACTGTATAAATGTTTAAGGTACAGATATATCTGAATGAATTTGATTGTTTCACTACTGATATTTCCATTTTATTCAATACTGTTTTTCACTCTGTGCAATTTTCACATTTTTGTTTGAGTTAATTTCGTATTTAATATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21120
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098503 Nonsense 378 794 10 16
ENSDART00000133410 Nonsense 40 289 1 7

The following transcripts of ENSDARG00000068210 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 65674903)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58856643
GRCz11 7 59159073
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATCAAGGTTTCCATTGGGAAGCTAGAGGAAGAATGGGAGTGCAAGTG[G/A]GCAAACTGTTTGAAAAATACACCCCTCACGTGTTTTCTTGAAGAGGATCC
Long Flanking Sequence:
TTTTATATTTAGAAAAAGTGTTGTAATGATGGTGAGGTACAGTTCAGTTTAGTTTTTGTAATTTATTTAAACCATAAAGTAACAAAGGTAAAACAAACTTTTTTTTTTTTTTTTAAATCAACCATCAATCAGAACTAGTTTGAATTACATTGACACAATAAAAAAAAATAAATGAACAAACCAGGGATTTGAAAATCACTGTCAGCTGTGAGTTAATTGATCAACATCAGGTTTAATTCATGAGTTGCTAGTTTAAATCTGTGACCACGCCCTCTGTGTTAAGAGTCTACTGAAATATAAAGGTATGTGAAGGGACAAAGTGAATTTGGGACCTTTACTAATTATTAAGCTCAATATTGATCAAACTATTGATTAGATTAAATGGTTTTTGTGAAAATTTACTATTTTACTTTTTTTTCTAGGTGGAAATTGGTCAAAGAAGATGCAGCAGAGATCAAGGTTTCCATTGGGAAGCTAGAGGAAGAATGGGAGTGCAAGTG[G/A]GCAAACTGTTTGAAAAATACACCCCTCACGTGTTTTCTTGAAGAGGATCCTGTAAGTGGAGTCACAACAACTTTTCTTGTTTTATTTCTATGTTGTGCATTTTTTTAAGGTTGTTTAGGGTACTGGTTTCTTTTGTGTCAGATTTTACAGAAGTAACACATTTGGTTTAGTTTCTTTTGCTTTAAAATGATCAGTTTTCTGCATCTCTTAACAGGTTCTTGACTTAGTATCTCCAATGGTTGCTCTCTCATTTGAGCCAGCTTCTGAGGCTAGCTTTCAGGCTAGTGTCATTTCACAGTATCCATGTAAACCACATGGTAAGTTTACAGCTCAAGTTGCTCCTTGAATAATATTTTTCCCCATAGAGATGCTGCAAATTTTTTTTCTCTTGCTTTCAAGACCTGCTTGAGCAGCCATCAAAAGAAAAACTTGATACCACAGTGGCAGTCGTTCATTTGGAACAAGAAGTTCACCTGAAGCCAGAGATCAAAATGTATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5451
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098503 Essential Splice Site 580 794 15 16
ENSDART00000133410 Essential Splice Site 242 289 6 7

The following transcripts of ENSDARG00000068210 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 65673202)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 58854942
GRCz11 7 59157372
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCCCTTTTCATCTAGGAAACAACTTTGCCGCACTCCTGAGAGTCTAAG[T/A]ATGTGTTTGGTAGCCTAAACAWGTAGTATTCTCTACTTTATTAGAAATGT
Long Flanking Sequence:
TGTATTAAAGACCAAGGCTCAAATTCTAGACTTAGAGTGTGACAACTTGGCAAGTCAAGTATGTGTGTGTTTTTGACTAAATAAGTTTTGCTTCGTTGCAGTATAATAATACATAAAAATTATGCCATGTAGCACCAACTAAACTGGCTATGGTGGTGGGTTGTAGTTTTACATTTTTTGCAGTGGGAAACTGATACAAGGGCAGTGTTAAGCAGTACTCTACCCTTCACAAGTTTTCCCTATATCAAACCTGCTCTCTGATGACCGGTGCGAGTTGAGAGAAATCGCCACGGACAGATACGGGGCAGACATACAGTCTTACATACTTGTTAATGCAAATGTACCCAAACCTAATTACGGTTTGGTTCTCAGTTTGCAGATGCAGTGATCATGAGTCCAGGTAATCAAAGAAGTGATGTAGACCTTGGACAGTTACTAAATGCCATATCGGATCCCTTTTCATCTAGGAAACAACTTTGCCGCACTCCTGAGAGTCTAAG[T/A]ATGTGTTTGGTAGCCTAAACATGTAGTATTCTCTACTTTATTAGAAATGTTGTGTTTAAACATTTGGATTTTAACACAAACTATCTTTTAGTTAAAGATGTCAGAAGTTCATGGAGAAAAGCTGTGGAGGAAGGATTGGCTGAGAAGAAACAAGCGTCTTGGAATCAGCAAGACAGCCTTTCTTGGCTCAAGACACCCATGGCTAATATGAACAGCCCGTGCAAGACCCTAAATTTAGAGTCTTCCATGTCTTTTTCAACCAATCTTGACAATTGCACTTCTCCTCCTGTCCAGCAGGGGTCTACCCTTCACTCAACTTTGTCGTGGGACTCCTCACAAATGGAGGTGCTTACCAGTCAATGCTCAAGTGATGTTATTAAATTCAGCATTGCTCAAGAGGAGCCCCCAGACCTGTTTGATGTATCATTTAACAGCGACAGCTCTGTTGAGAATTCTGGTGAAAAAGCGAGGGATGAAGAACTTTGCTTGCCATCTGTTGG
Associated Phenotype:
Not determined