ZMP
nbr1
Ensembl ID:
ZFIN ID:
Human Orthologue:
NBR1
Human Description:
neighbor of BRCA1 gene 1 [Source:HGNC Symbol;Acc:6746]
Mouse Orthologue:
Nbr1
Mouse Description:
neighbor of Brca1 gene 1 Gene [Source:MGI Symbol;Acc:MGI:108498]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11901 | Essential Splice Site | Available for shipment | Available now |
sa22111 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11901
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114556 | None | 274 | 1014 | 9 | 23 |
ENSDART00000133048 | Essential Splice Site | 268 | 989 | None | 21 |
The following transcripts of ENSDARG00000077297 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 28790001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27127610 |
GRCz11 | 12 | 27218970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTATATRTWTGTTAAGGGAATTGAATTCATTTTTCTGTGTTGTTTTC[A/C]GGTTTCTGAGGCGGGGTGACAGGACGGTGAGAAAGGCGGAGAGGCAGCGT
Long Flanking Sequence:
GAGGAGCAGATTCACATTTACATTTAGAGAAGATGGAGGGGTAGAATTTATTAAGCTTAACCCTACAATAATGAATCTGGTGTACTATTTTATATTAAATTAGTTGGTGTCTTGAGTTAATAGAACAAGTGTTTATGGTATTAGTAATTTAAAATTTATTTAAGATTACAATTCAGAAGTACTCTTCCAATCTCACACTATTTGAGAAAATGAATGACCGTTCAATATGAACTCTTCCCTCCTCCTATGTGCAGTGTTTGTCCATCTTGCATCTTATGCGAGCCATGCAGTCATAAACACGATCCCAGCCACAACCTAAAGAGAACAAGGACTCCTCTGTCTGTCCCTGAACGTGGAGTTACCCCTGAACCCAGGTAGGCCAAAATAAACACTTGGTGCTCAAGATGTTGTGAATTTTCTGCTTGACCTAACGTGTTGTTTAGAGCGATGATTGTATATATATGTTAAGGGAATTGAATTCATTTTTCTGTGTTGTTTTC[A/C]GGTTTCTGAGGCGGGGTGACAGGACGGTGAGAAAGGCGGAGAGGCAGCGTCTAAAAGCAGAGCGGAGGCAGCTGAAGGCTGAGGTGAAGGAGATCAAGAAGAAGCTGAGGCTGGAGAAGAGAGGTCTGCTGTGGAGTGGAGCCTCCAACGGGACCAGCACCTCAGGCCTTGCCCCCGCTCCCGCCCCGTCTCTAGGTGCAGGACCAGCCCCAGCTCCGGCCCTGTGCCCAGACCCTCAAACTTCCAGTCCAGAGTAAGGGCCACACTGAGAGGGGTCAGGGCTGGGTGACCTCCCTACCCAGCCCAGAACAAACATTATCAAGATTTATCACATTGTCTGTTATAGTTGAGTTATCGCTGGCAAATGGATGGAACTACCTCAAAATAGCACCCGCTGCCTTTATGTATTACGTCCTTTTTTGTACTTTTTTGATATGAACTTCAAGGAAAAGACAGACGCTGAAACAAAGCTGTTCTGATGATCCTCTGTGCACTCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22111
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:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114556 | Missense | 699 | 1014 | 17 | 23 |
ENSDART00000133048 | Essential Splice Site | 692 | 989 | 16 | 21 |
The following transcripts of ENSDARG00000077297 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 28792643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27130252 |
GRCz11 | 12 | 27221612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGTTCCTGTGTCAAAGCCAATCATAACAGATGAACCTGTCTTTCCAG[G/A]TCTGCATGCCTTTTTTTTTTCTTGGTCACTGTTACTTAGGGTGCTTTTAC
Long Flanking Sequence:
GATTTTTAGATCTGTTAAAGGCTTTTGTGAATGAATGTCTTCCTGAACTGATTATGAACGTGTTACTAGTGACCTTTTATGTACTGACACGACTTATTCTCTGTTAGTCCTGCAGCCTCAGAGACAAAACGAGCTTCTGGATGTTCCAGGCAATGAGGAAGGAGACGAAGACATCAGTGGCACTCAGTTTGTGTGTGAGACTGTGATTCGCTCTCTGACTCTTGAGGAGGAACCAGAACGCAAACCTCAACGCAGAGCACGGCCCAGCCTGAGGAGGCATGATGGTGAGCTTCTGCTGGAATTCTGCTCACAAAAAAACAGATATTTGACTGGCCTTATTTTGTTTTTGTTCATTTTGCCTTCCTATTTTGCAGTTCCAGATCCTGTTCGCTTAAAGGAGAGATCAGTGCCGGTGAAGAATGACAGACCAGTCATAAACAGGCCTGAGGCTCCAGTTCCTGTGTCAAAGCCAATCATAACAGATGAACCTGTCTTTCCAG[G/A]TCTGCATGCCTTTTTTTTTTCTTGGTCACTGTTACTTAGGGTGCTTTTACACTTGGTTTAATTGCCTGGACCATACCAAAGTTCGATTGTCCTCCCCGGCCACCTTCTCGGTTGGTTTGTGTTCACACTTTCTTTTTTCCTTCTGAACCCCGTTACGCTTGCTTCATCAAGCTGCTGTGGTGTGTACAGCCTTTGGTTTTGGACATACAGAAAAGCAACTCGCGTCCATCTGTCGCAATATTATTATAAAAGTTCAGAACATAACGCAATGTTTTTGGAGGAGACAAGCAGACATTATCACTATGCTTGCCCTGGCTTAGTCCTGCTTGTCACCAAGGTACAGTACGTGATACACACACATACACACACACGAATGAACGTTATGAAATGCTGTTGATGGATCCATTATTTGGTACGATTGCATTCATATCAGAAGTGAAGCGGACCAGGACCGTACCCCAGACCACCTCTTTCAGCTGGACTCTGGTATATTTTGTGAG
Associated Phenotype:
Not determined