si:ch211-72g23.1

Ensembl ID:
ENSDARG00000075098
ZFIN ID:
ZDB-GENE-090313-131
Description:
Novel protein similar to H.sapiens WDR17, WD repeat domain 17 (WDR17) [Source:UniProtKB/TrEMBL;Acc:B
Human Orthologue:
WDR17
Human Description:
WD repeat domain 17 [Source:HGNC Symbol;Acc:16661]
Mouse Orthologue:
Wdr17
Mouse Description:
WD repeat domain 17 Gene [Source:MGI Symbol;Acc:MGI:1924662]

Alleles

There are 7 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa32719 Nonsense Available for shipment Available now
sa32720 Essential Splice Site Available for shipment Available now
sa38280 Nonsense Mutation detected in F1 DNA During 2017
sa30584 Nonsense Mutation detected in F1 DNA During 2017
sa31216 Nonsense Available for shipment Available now
sa19535 Nonsense Available for shipment Available now
sa39649 Essential Splice Site, Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa32719
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Nonsense 92 1292 2 29
ENSDART00000136300 Nonsense 92 1283 2 28
Genomic Location (Zv9):
Chromosome 1 (position 39132744)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38060006
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTGCCAGTGCCAGCGCTGATAACCTGCTCATCATCTGGAATGTGGCTGAG[C/T]AGAAGGCTGTCGCAAGGCTAGATAACACCAAAGGTATAATCCCTACAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32720
Current 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:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Essential Splice Site 303 1292 5 29
ENSDART00000136300 Essential Splice Site 305 1283 5 28
Genomic Location (Zv9):
Chromosome 1 (position 39135784)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38063046
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACTGGCTTCCACGCACTTCATGTTTTAAACTCCCCACCAGCAAAGAAATG[T/A]ATGTGTGTATATTTTTACCATATAGTGCATATCATAAATGAGCACATGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38280
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Nonsense 571 1292 12 29
ENSDART00000136300 Nonsense 573 1283 12 28
Genomic Location (Zv9):
Chromosome 1 (position 39141434)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38068696
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ACACATGAATATGTGTTTATGTTGACCAGGACTGTCCGTATCTGGGATTA[T/A]ACCCAAGACGCTTGCATTAACGTGCTAAGTGGTCACACCGCTCCAGTGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30584
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
G > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Nonsense 674 1292 13 29
ENSDART00000136300 Nonsense 676 1283 13 28
Genomic Location (Zv9):
Chromosome 1 (position 39145775)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38073037
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CACTCCTCTAATCGCTCCCTTAGTAGTCAACATCCTCACTGACCACAGCT[G/A]GGACGACATTATTGGCAACACAGGTTAAAACATATGAGCGTATTAAATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31216
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Nonsense 705 1292 14 29
ENSDART00000136300 Nonsense 705 1283 14 28
Genomic Location (Zv9):
Chromosome 1 (position 39145947)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38073209
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTCCCGGGGCTCCTCCTTTGTTGTGTGGAAAGGTTTCCCGAGATATCAAA[C/T]AGGAACTAGATAAACTCTCAAGTGACGTGCGCATGAAGAAGCTGCGGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19535
Current 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:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Nonsense 808 1292 16 29
ENSDART00000136300 Nonsense 808 1283 16 28
Genomic Location (Zv9):
Chromosome 1 (position 39146470)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38073732
KASP Assay ID:
2259-0838.2 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GTAAAGAGGAAAGGCTCAAGAATGCAGCTGAAATCCATATCAGACTGGGT[C/T]AAATCCAGAGATACTGTGAGCTCATGGTGGAACTGGGAGAGGTAAAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39649
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
A > T
Consequence:
Essential Splice Site, Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110824 Essential Splice Site 1190 1292 28 29
ENSDART00000136300 Splice Site None 1283 None 28
Genomic Location (Zv9):
Chromosome 1 (position 39156463)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 38083725
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTAGTAAAGAATATATTTAAATATGTTCTTTGTTTTCATTTTTTTTACAC[A/T]TACATAGAGTGGCAGATGACAGTTTGTATACTTCACCATCTGAGGCCCAG
Associated Phenotype:
Not determined

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