ZMP
nucb1
Ensembl ID:
ZFIN ID:
Description:
nucleobindin-1 [Source:RefSeq peptide;Acc:NP_001038928]
Human Orthologue:
NUCB1
Human Description:
nucleobindin 1 [Source:HGNC Symbol;Acc:8043]
Mouse Orthologue:
Nucb1
Mouse Description:
nucleobindin 1 Gene [Source:MGI Symbol;Acc:MGI:97388]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33192 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20030 | Essential Splice Site | Available for shipment | Available now |
sa15054 | Nonsense | Available for shipment | Available now |
hu7895 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33192
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077089 | Essential Splice Site | 38 | 454 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 30303840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30021879 |
GRCz11 | 3 | 30152721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCGCAACCCAGACCCTCCTCAGGAGGAGAAAGCAGAGGAGAATGTGG[T/C]AAGACGGCTCTCGCATCATGCTGTCAGAGCTCATCTTGTGCTCTCAGCAT
Long Flanking Sequence:
AGGAGCGCTGAGTAATCTGTAGTCACTCAACGCTCCAACCGGATCTGACCCTGTGGTAAGAGAACTCGCTGTTTATTTGACATAAAATGAAGAGATTCACGCTAGATGACACTGCAGTGTGGGTGGCCGTGACACACATATGTGTGGCCGTTTTTCACTTGAAGTTGAAGCTGTTGTGAAAGATGTTCGGAGTGTTTTCTCGAGCTGTCCTACAGACTTCCTTTCTTCGGCTGCTTCCTCTTTCTCCTGTCCTAATCGATGTTTCTCATTAACCTGTCTGCTTAAAGAGGCCGTTCTAACCATTTCATGTAGAGTTATACCTTCAGGATGAAACTGACGGCTGTCATATCAATGTTCATCTGCTTTTTTGCCAAGGTGTGTAAGGATGACAGGAAGCTTTAAAGCTCTGCTGCTTCTGTCTCTGTGTCTGCTGGTTTGGGCAGTGCCAATAGACCGCAACCCAGACCCTCCTCAGGAGGAGAAAGCAGAGGAGAATGTGG[T/C]AAGACGGCTCTCGCATCATGCTGTCAGAGCTCATCTTGTGCTCTCAGCATTTTGTTTAATAAGCAAATGCACTTGTTTTGTTTTTGTGTATATCAGGACACTGGACTGTACTATGACCGTTACCTCAGAGAGGTGATTGAGGTGCTGGAAACAGATCCTCACTTCAGGGAAAAACTGCAGACTGCCAACACCGAGGACATTAAGGTAAACAAAAAACTATGTCAGGCACAACATCATGCCTGAATATATATTTAATATAAAGAAAGTTATCTATGCATTTTTATTATTTAAGACCATGTACCATGATCTGAGAGACCAATCAAATGTATAAGAAAGGGTTGCCACTGGGTCTTAAAATCTTAAAATGACAATAAATTTCAAAAACAGTATATGAGGCATTATAAAGTCTTAAATTCACTGAAATATGGTGTTGTAGGTCTTAAATTATTTTAAACAGGTTCAACTTAGTCCAAGTAAAGCTACCCAATGTGGCCGACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20030
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 |
---|---|---|---|---|---|
ENSDART00000077089 | Essential Splice Site | 119 | 454 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 30301981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30020020 |
GRCz11 | 3 | 30150862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTCAGGATGCTGCTGAAGGCTAAACTGGACAGCACCAATGCCCAGAG[T/G]CAGTGTGTTTATGCTTGTGTTGCACTCAGTTGTGCTGATGAATGAGGAAA
Long Flanking Sequence:
ACTTTACTGTAATCTGGCTTTGAGGAGGTATGAATGTACAGAAGTTTAAAGAGTTATGTAACCGTTTTATCCATATTATCCATTATACATGTCTATGGATTTAACCCTTCAAGCACATCTAGGTTACTAAGGGTTGACATATCATTATTTTATTTTGAAGGCGATTCAATTATTGCTGGGGACATTTCAGGAATTGGTGGATATTGGTGGGGTCATGTCCTCTCCATCCATGCATATTCTCTATAAAAACTTTATATTTTCATACCTTTTAATTTCATTTCAACTTTGAAGTGCTAGTCATTGCAAAGATGTTTGGTTTACTACTTTTCCATTTCAGGCTCATAATAAAATGATCCTGTGTTTCAGAACGGACGCCTCAGTAAGGAGTTGGATTTGGTGGGTCATCATGTCAGAACTCGACTGGACGAGCTAAAGAGGCAGGAGGTCTCGCGCCTCAGGATGCTGCTGAAGGCTAAACTGGACAGCACCAATGCCCAGAG[T/G]CAGTGTGTTTATGCTTGTGTTGCACTCAGTTGTGCTGATGAATGAGGAAATCTGTCGATGTGACTCAAATGTGAATGTTTGATTGTGACTGCAGGTGTTCAGATGGATCACGCCTCCTTGTTGAAGCAGTTTGAACATCTGGATCCTCATAATCAGAACACTTTTGAGGCCAAAGACCTGGAACTGCTTATCGCCACAGTAAGATCTGTTCCTAGCATGCCAGAATGGTAAACTGGACAAGATAAGATCACAAAACTGTAAATAGACAAGCATACACGTGGTTAATGTTAGTTAATGTAACATGAATAAACAATATTTTTATTACAGAATATATAATCTTTGATAATATAAGCTTAAGGCTGATTTATACTTCTGCGTCAAACGCCGGCGTATGCTACGGCGCTGACGCATAGCCCTTCGCCGTGGCCGTCGCCGTCACTGACGTGCACCTCTCAAAAAATGTAGCGTAGCGTAAGCTCTGTGATTGGTCGGCTTGGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15054
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077089 | Nonsense | 350 | 454 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 30294789)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30012828 |
GRCz11 | 3 | 30143670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTSTATACAGAAGAGGAGCTGCAGCRCTTTGAGACAGAACTTCGGGAT[A/T]AAGAGCTGGAGCTCGGCAGAAGAGCAGAGAAATTAAGACAGGAGCAGGAA
Long Flanking Sequence:
TAGGTAAGTTTTAAATGGTGAAATTAAGATAGAATTAAGATGCTAATGGTCTAATGCGATTCAATGACCTGCTCTAAGCTAAAAGTACACCCAGAGATCAGCTGAATGATTCAAAAATGGTAAAAGTCAATTTTTTAACTGTAGGGGACTTGTAAAATAAGCCTATTTCCAAAAAAAAGTCAAATGTTCCTTTAAATAGTTTAACATACCTGCTAAAACAGACCCTTTTTCCCCTCTCTCTCTTACACTGTAGGTGGATGTCAATCACGATCGTCTGGTCAGCCTGGAAGAGTTTCTCAAATCCACAGAGAAGAGAGAGTTAAACAACCAAAAAGAATGGGAGGTCAGAGTCTGATTTAGATGCATGCTTGGCTTTTATGATATTGTGTTTTCAATATGACAGGGTTTTAAATCATTACCCGTTTATATAGACGCTGGATGACACAAAGCCGGTGTATACAGAAGAGGAGCTGCAGCGCTTTGAGACAGAACTTCGGGAT[A/T]AAGAGCTGGAGCTCGGCAGAAGAGCAGAGAAATTAAGACAGGAGCAGGAACTTCTGAAAGAGAGAAGCAAAGCTCTTGAAGCACAGAAACGAGAATATCAGCAGGTAAACGGTGTCAAATGTAACAGAGGTGGTTGCTTCACCTCTAGGGCACTTTGTTTTGTCATTTAACAGCGGTTTCAAATTGGGCTTGACATTTATCGATTTTTATTTATTTTTTTGTTCTGATTTTATAAAGAGAATGTTTGAAAGTATAATCATATTTTTAATTAGTCACATTTCTTATGTAACTGTTTATTACATAAAAATACAATTTATTAAATCATTTAAAGCAACATGTAGTTGCAATCAGAATTGTTAGCCCCCCTTTGAATTTTTTTCTTTTTAAAATTTTTTTCCCAAATAATGTCTTAACAGAGCAAGGACATTTGTACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTTTTGTTTGTTTTATTTCTGCTAGTATAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu7895
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 |
---|---|---|---|---|---|
ENSDART00000077089 | Nonsense | 380 | 454 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 3 (position 30294699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 30012738 |
GRCz11 | 3 | 30143580 |
KASP Assay ID:
554-2391.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAGCAGGAACTTCTGAAAGAGAGAAGCAAAGCTCTTGAAGCACAGAAA[C/T]GAGAATATCAGCAGGTAAACRGTGTSAAATGTAACAGAGGTGGTTGCTTC
Long Flanking Sequence:
CCAGAGATCAGCTGAATGATTCAAAAATGGTAAAAGTCAATTTTTTAACTGTAGGGGACTTGTAAAATAAGCCTATTTCCAAAAAAAAGTCAAATGTTCCTTTAAATAGTTTAACATACCTGCTAAAACAGACCCTTTTTCCCCTCTCTCTCTTACACTGTAGGTGGATGTCAATCACGATCGTCTGGTCAGCCTGGAAGAGTTTCTCAAATCCACAGAGAAGAGAGAGTTAAACAACCAAAAAGAATGGGAGGTCAGAGTCTGATTTAGATGCATGCTTGGCTTTTATGATATTGTGTTTTCAATATGACAGGGTTTTAAATCATTACCCGTTTATATAGACGCTGGATGACACAAAGCCGGTGTATACAGAAGAGGAGCTGCAGCGCTTTGAGACAGAACTTCGGGATAAAGAGCTGGAGCTCGGCAGAAGAGCAGAGAAATTAAGACAGGAGCAGGAACTTCTGAAAGAGAGAAGCAAAGCTCTTGAAGCACAGAAA[C/T]GAGAATATCAGCAGGTAAACGGTGTCAAATGTAACAGAGGTGGTTGCTTCACCTCTAGGGCACTTTGTTTTGTCATTTAACAGCGGTTTCAAATTGGGCTTGACATTTATCGATTTTTATTTATTTTTTTGTTCTGATTTTATAAAGAGAATGTTTGAAAGTATAATCATATTTTTAATTAGTCACATTTCTTATGTAACTGTTTATTACATAAAAATACAATTTATTAAATCATTTAAAGCAACATGTAGTTGCAATCAGAATTGTTAGCCCCCCTTTGAATTTTTTTCTTTTTAAAATTTTTTTCCCAAATAATGTCTTAACAGAGCAAGGACATTTGTACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTTTTGTTTGTTTTATTTCTGCTAGTATAAAAGCAGATTTGATTTATTTTTTTTAAAACATTTTAAGGTCAAAATTATTAGCCCCCTTTAAACTATACATTTTTGATAGTCTACAGAACAAAC
Associated Phenotype:
Not determined