ZMP
LOC568786
Ensembl ID:
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa645 | Nonsense | F2 line generated | Not yet available |
sa39183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16236 | Nonsense | Available for shipment | Available now |
sa39182 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa645
Status:
F2 line generated
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:
T > A
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | KN150342.1 | 56736 |
KASP Assay ID:
554-0554.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGGCAGCCAGGTGGAGATCKTTCACTCCAATGTGGTATTTGATATCTG[T/A]AGTCTGATGCTTTATGGGACGCAGGCGATCCCAGTGCGTCTGAAGATCCT
Long Flanking Sequence:
TGGTTGAGCTGAACATGAAATTAATATTCCTTTAAAACATTTAAACAGAATATTTCTGTTCATTCTATGTTATTCACAATTTAAATATACTTTGTCTTCAAAATGAAATATGGGTATGTTGATGGCTCAGGATATATGTGATCGTAATCGTCCACCATTGTAGATGATAATCGTTAATAATGCAGTCTTTAAGTTTTCAGTTATGCACGATGCTAATTGTGCAGAAAAAGATCTTTATTCTAGTACATATGCAATGGCCAGAAAGAAATATTCTAAGTTATGCAATCGAGGATTTAAATCCTACAAAAAAGATGCATTCAGAAATAAATGACAAAAATGCTTTCATCAAACACACCGAGACGCTCTGCTGGTTTCTGCACGTGTCATGTTAACTGCTTTCTGTTTTGCTAAATTGCAGCTCTGAGCAAGCTGAAGGTTCATCACATGTACCAGGGCAGCCAGGTGGAGATCGTTCACTCCAATGTGGTATTTGATATCTG[T/A]AGTCTGATGCTTTATGGGACGCAGGCGATCCCAGTGCGTCTGAAGATCCTGCTGGACCGACTCTTCAGCGTCCTCAAGCAGGAGGAGGTTATTCAGATCCTCAATGCGCTGGACTGGACTCTACAGGACTACATCCGCGGATACGTCCTGCAGGTCAGATGCTTTTTCTTTCACTGCACTAATTTTTGATCTATAATTACAGATTTGTCGCACTTTACCTAAGAAAATAACCAGAGGAGAGCCACTGAGATTTCTGCCTTCAATTTGCTTATCAAGTATTCAGGTGCTTGAAATAAATTCATGGTAGTTCCTCTGGTGGAGAATGTAAAGTTAAAGCCTCTTCAGACCTCCAGATGAATGCTGTATGATGAAATATTTATTCTGGTTACAACACGAAGCTGCTGCATGACTTTCAAAGCCTGCTGGCACTCAAGAGTAATTACAGGCGGACTGAAAGAGTTGCCCGACTCGCCTCTGATCTCTCCCCTCCCCTCCTGCTC
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
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 > A
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | KN150342.1 | 55576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAATACAGACTCCGACCACCAGGAGGTGCAAAACAGGCACGACGCTT[C/A]AGAAATAAGCCTGGACAGTGTTTCACCGTTCGAGTCTGGCCCCGTGAGAA
Long Flanking Sequence:
AAAGTCCAAGAGCAGAACATTTGTTGCTTTAATATTCATGATTCCAATGACATTCCTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCCAGGACGTGGCTGGTAAGGTGTTGGACCGCTGGGCGATAATGACCTTTGAAGAGGAGATCGTCACGCTGCAGCAGTTCCTCCGATTTGGGGAGACCAAATCCATCGTGGAGCTCATGGCCCTGCAGGATAAGGAGGGACAGGCTGTTGTTGTCTCCACCACCAAGACCAATTCTGACATCCGCAGCTTCATCGAGAGCAGCACGCAGCGCTCGGTACGCCTGCCTGCTAAAGCGGATGCCCCTGGCTGCAGTAATGGGCACCACTTCGAGACGCTGGTCAACAGTATGGCGCTCATGTTGCCGCTGCAGCTTATGAACTCGGTGCCCGCGCCGCTGCTGAGTTGCAATACAGACTCCGACCACCAGGAGGTGCAAAACAGGCACGACGCTT[C/A]AGAAATAAGCCTGGACAGTGTTTCACCGTTCGAGTCTGGCCCCGTGAGAACAGACGTGTTGCTGAACAGCGAATCTCCAAAGATGGAATCGGAAGAGTTTAACGTGAGCGGAAACTCCTCTCCGTCCACGAACTGCACACCCTCCGTCCACTCCGAAATCACACACCTGTCTCCGGAGAGCAAGATCCGGTGTGCAGAGAAGAGCGGATCGCTGAAGAAGGGCCGCGTGTTCTGCAGCGCCTGCGAGAAAACCTTCTACGATAAAGGCACGCTGAAGATCCACTATAATGCAGTTCACCTGAAGATCAAGCACAAGTGCACCATCGAGGGCTGCAACATGGTGTTCAGCTCCTTACGCAGCCGGAACCGACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAATAATCGTGACAAAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGACGAGAAGAGAGAGTTCATTCCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16236
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:
C > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | KN150342.1 | 55208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACCATCGAGGKCTGCAACATGGTGYTCAGCTCCTTAYGYAGCCGGAAC[C/T]GACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAAY
Long Flanking Sequence:
ACCACTTCGAGACGCTGGTCAACAGTATGGCGCTCATGTTGCCGCTGCAGCTTATGAACTCGGTGCCCGCGCCGCTGCTGAGTTGCAATACAGACTCCGACCACCAGGAGGTGCAAAACAGGCACGACGCTTCAGAAATAAGCCTGGACAGTGTTTCACCGTTCGAGTCTGGCCCCGTGAGAACAGACGTGTTGCTGAACAGCGAATCTCCAAAGATGGAATCGGAAGAGTTTAACGTGAGCGGAAACTCCTCTCCGTCCACGAACTGCACACCCTCCGTCCACTCCGAAATCACACACCTGTCTCCGGAGAGCAAGATCCGGTGTGCAGAGAAGAGCGGATCGCTGAAGAAGGGCCGCGTGTTCTGCAGCGCCTGCGAGAAAACCTTCTACGATAAAGGCACGCTGAAGATCCACTATAATGCAGTTCACCTGAAGATCAAGCACAAGTGCACCATCGAGGGCTGCAACATGGTGTTCAGCTCCTTACGCAGCCGGAAC[C/T]GACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAATAATCGTGACAAAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGACGAGAAGAGAGAGTTCATTCCCATCCCGGAGAGCCGCAACGTCTCCAGTTTTATAATTCGCAATTCCGAGCCCAAACTGCACGGCTCACTGTCGGGCCTAAGCCAGAGCGGCATCCTCTTTCCCAACCTGAAGACAGTACAGCCAGTGCTGCCCTTTTACCGCAGCCTGGTGACCCCGGCTGAGCTGGCACACACGCCGGGCAGCCTGCCCTCCCTGCCACTGTTGTCCTCCTCTGTGCCCGCCGGCTCCAGACACATGCTGATGGACACGGTGCCCAAGAAGAAATCTCGCAAGTCCAGCATGCCAATCAAAATCGAGAAAGATGAGCTGGCGGAGGAGGGTGTGTCTGAAGAAGAGACTCCGCCCCTCAGCCCCTGCACAGAAAACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39182
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 > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | KN150342.1 | 55097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGAC[G/T]AGAAGAGAGAGTTCATTCCCATCCCGGAGAGCCGCAACGTCTCCAGTTTT
Long Flanking Sequence:
TGCAAAACAGGCACGACGCTTCAGAAATAAGCCTGGACAGTGTTTCACCGTTCGAGTCTGGCCCCGTGAGAACAGACGTGTTGCTGAACAGCGAATCTCCAAAGATGGAATCGGAAGAGTTTAACGTGAGCGGAAACTCCTCTCCGTCCACGAACTGCACACCCTCCGTCCACTCCGAAATCACACACCTGTCTCCGGAGAGCAAGATCCGGTGTGCAGAGAAGAGCGGATCGCTGAAGAAGGGCCGCGTGTTCTGCAGCGCCTGCGAGAAAACCTTCTACGATAAAGGCACGCTGAAGATCCACTATAATGCAGTTCACCTGAAGATCAAGCACAAGTGCACCATCGAGGGCTGCAACATGGTGTTCAGCTCCTTACGCAGCCGGAACCGACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAATAATCGTGACAAAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGAC[G/T]AGAAGAGAGAGTTCATTCCCATCCCGGAGAGCCGCAACGTCTCCAGTTTTATAATTCGCAATTCCGAGCCCAAACTGCACGGCTCACTGTCGGGCCTAAGCCAGAGCGGCATCCTCTTTCCCAACCTGAAGACAGTACAGCCAGTGCTGCCCTTTTACCGCAGCCTGGTGACCCCGGCTGAGCTGGCACACACGCCGGGCAGCCTGCCCTCCCTGCCACTGTTGTCCTCCTCTGTGCCCGCCGGCTCCAGACACATGCTGATGGACACGGTGCCCAAGAAGAAATCTCGCAAGTCCAGCATGCCAATCAAAATCGAGAAAGATGAGCTGGCGGAGGAGGGTGTGTCTGAAGAAGAGACTCCGCCCCTCAGCCCCTGCACAGAAAACTGTGGTGTCAGCAACTCGGGCCGTGAGGATGGCGAGGATCTTCTGTTGACCACCGTGGACACCCAAGACACTCAGTGGCACAAACTGACCCATGAGGACAGTTGCATCATCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31018
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:
A > T
Consequence:
Nonsense
Transcripts:
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 |
GRCz11 | KN150342.1 | 55025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGGAGAGCCGCAACGTCTCCAGTTTTATAATTCGCAATTCCGAGCCC[A/T]AACTGCACGGCTCACTGTCGGGCCTAAGCCAGAGCGGCATCCTCTTTCCC
Long Flanking Sequence:
CAGACGTGTTGCTGAACAGCGAATCTCCAAAGATGGAATCGGAAGAGTTTAACGTGAGCGGAAACTCCTCTCCGTCCACGAACTGCACACCCTCCGTCCACTCCGAAATCACACACCTGTCTCCGGAGAGCAAGATCCGGTGTGCAGAGAAGAGCGGATCGCTGAAGAAGGGCCGCGTGTTCTGCAGCGCCTGCGAGAAAACCTTCTACGATAAAGGCACGCTGAAGATCCACTATAATGCAGTTCACCTGAAGATCAAGCACAAGTGCACCATCGAGGGCTGCAACATGGTGTTCAGCTCCTTACGCAGCCGGAACCGACACAGCGCCAACCCCAACCCACGGCTGCACATGCCAATGAACCGCAATAATCGTGACAAAGACCTGCGGGGTGGCCTGAGCCCGGGCCTAGAGGATGGGCAGGAGGACGAGAAGAGAGAGTTCATTCCCATCCCGGAGAGCCGCAACGTCTCCAGTTTTATAATTCGCAATTCCGAGCCC[A/T]AACTGCACGGCTCACTGTCGGGCCTAAGCCAGAGCGGCATCCTCTTTCCCAACCTGAAGACAGTACAGCCAGTGCTGCCCTTTTACCGCAGCCTGGTGACCCCGGCTGAGCTGGCACACACGCCGGGCAGCCTGCCCTCCCTGCCACTGTTGTCCTCCTCTGTGCCCGCCGGCTCCAGACACATGCTGATGGACACGGTGCCCAAGAAGAAATCTCGCAAGTCCAGCATGCCAATCAAAATCGAGAAAGATGAGCTGGCGGAGGAGGGTGTGTCTGAAGAAGAGACTCCGCCCCTCAGCCCCTGCACAGAAAACTGTGGTGTCAGCAACTCGGGCCGTGAGGATGGCGAGGATCTTCTGTTGACCACCGTGGACACCCAAGACACTCAGTGGCACAAACTGACCCATGAGGACAGTTGCATCATCTCACCATCCTCTCCTTCCATCTTTCACATTAAACAGAACAGCGAGAAAGAGGAGTCCTTAAAATGTGAAGAGCCA
Associated Phenotype:
Not determined