LOC568786

Ensembl ID:
ENSDARG00000074397
Human Orthologue:
BNC1
Human Description:
basonuclin 1 [Source:HGNC Symbol;Acc:1081]
Mouse Orthologue:
Bnc1
Mouse Description:
basonuclin 1 Gene [Source:MGI Symbol;Acc:MGI:1097164]

Alleles

There are 5 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa645 Nonsense F2 line generated During 2016
sa39183 Nonsense Mutation detected in F1 DNA During 2016
sa16236 Nonsense Available for shipment Available now
sa39182 Nonsense Mutation detected in F1 DNA During 2016
sa31018 Nonsense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa645
Current Status:
F2 line generated
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 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109108 Nonsense 63 867 2 4
Genomic Location (Zv9):
Chromosome 18 (position 79276)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150342.1 56736
KASP Assay ID:
554-0554.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CAGGGCAGCCAGGTGGAGATCKTTCACTCCAATGTGGTATTTGATATCTG[T/A]AGTCTGATGCTTTATGGGACGCAGGCGATCCCAGTGCGTCTGAAGATCCT
Associated Phenotype:

Normal

Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037
whole organism
ZFA:0001094
quality
PATO:0000001
normal
PATO:0000461

Mutation Details

Allele Name:
sa39183
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 2016.
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109108 Nonsense 244 867 3 4
Genomic Location (Zv9):
Chromosome 18 (position 78116)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150342.1 55576
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TTGCAATACAGACTCCGACCACCAGGAGGTGCAAAACAGGCACGACGCTT[C/A]AGAAATAAGCCTGGACAGTGTTTCACCGTTCGAGTCTGGCCCCGTGAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16236
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109108 Nonsense 367 867 3 4
Genomic Location (Zv9):
Chromosome 18 (position 77748)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150342.1 55208
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCACCATCGAGGKCTGCAACATGGTGYTCAGCTCCTTAYGYAGCCGGAAC[C/T]GACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAAY
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39182
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 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109108 Nonsense 404 867 3 4
Genomic Location (Zv9):
Chromosome 18 (position 77637)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150342.1 55097
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGAC[G/T]AGAAGAGAGAGTTCATTCCCATCCCGGAGAGCCGCAACGTCTCCAGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31018
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 2016.
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109108 Nonsense 428 867 3 4
Genomic Location (Zv9):
Chromosome 18 (position 77565)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150342.1 55025
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCCCGGAGAGCCGCAACGTCTCCAGTTTTATAATTCGCAATTCCGAGCCC[A/T]AACTGCACGGCTCACTGTCGGGCCTAAGCCAGAGCGGCATCCTCTTTCCC
Associated Phenotype:
Not determined

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