ZMP
bnc2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate basonuclin 1 (BNC1) [Source:UniProtKB/TrEMBL;Acc:Q1LYS3]
Human Orthologue:
BNC2
Human Description:
basonuclin 2 [Source:HGNC Symbol;Acc:30988]
Mouse Orthologue:
Bnc2
Mouse Description:
basonuclin 2 Gene [Source:MGI Symbol;Acc:MGI:2443805]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6591 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16752 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6591
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102322 | None | None | 172 | None | 2 |
| ENSDART00000125744 | Nonsense | 480 | 1141 | 5 | 6 |
| ENSDART00000128671 | None | None | 252 | None | 5 |
| ENSDART00000129074 | Nonsense | 450 | 966 | 4 | 9 |
| ENSDART00000134840 | None | None | 31 | None | 2 |
The following transcripts of ENSDARG00000069989 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 26163006)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 26503223 |
| GRCz11 | 1 | 27196937 |
KASP Assay ID:
554-5007.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGGCGGCCACCATTAAGTTTTGCCACCCCTCCTCTTGAGCCTATGAKA[C/T]AGTCACCTCTGCAGAGCCCACTTGTGTTCCCTTCTTTAAAGTCTGTGCAG
Long Flanking Sequence:
AGACACCAACACAACAGACACAGGGGCAACAACAGTCAAGTTCTCTGAACAATCACCAGATTCATCACCATTTTGAAAAAAATGAACAGTCAAAAACTATAACACACTCTTCTTTCTCCTCCAAAATGCATCGCATACGTCGCATGGGTGCGACATCACGTAAGGGTCGTGTCTGCTGCAACTCCTGTGGCAAGACTTTCTATGATAAGGGTACTTTAAAGATCCACTACAATGCTGTGCATCTGAAGATTAAGCATCGTTGTACTATTGAAGGCTGCAATATGGTCTTCAGCTCTCTGCGTAGTCGTAACCGACATAGTGCTAATCCCAATCCTCGCCTACACATGCCTATGCTGAGGAACAATCGGGACAAGGACCTTATTCGCTCCAGCTCTGGGACAGCCACTCCTGTCATATCAAGTACCAAAAGTGGCTTCAATCTAACTAGCCCAGGGCGGCCACCATTAAGTTTTGCCACCCCTCCTCTTGAGCCTATGATA[C/T]AGTCACCTCTGCAGAGCCCACTTGTGTTCCCTTCTTTAAAGTCTGTGCAGCCAGTGCAACCTGTGCCACCCTTTTATCGCACACTACTTTCTCCTGCTGACCTAGTTAGCCCCCCAGTCTCTCTGCCTACCAGTCCAATTCTGCCTACAACAGCTAACAGCACATCTCTTACGGACCAGCAACAGATGTTAGCTGTTAGCTCCCTTAGCATGCATGTATCCGAAACATCACCATTTTCTCATCGCTTACCCACAAATCACAGTACCCAAGATTCCATTATTCTTGATCCTATGCCTAAAAAGAAGCCTCGCAAGTCTAGCATGCCAGTAAAAATAGAGAAAGAGGTGATAGATGTTGCAGATGACTATGATGACAAAGATGAGGATGATGATGATGGAGACAGTTGTCACCATCACCATCATCAACCATCCAGCATCCATAATGTTAATGGCAACTGCAACAACAACAATAATGGCAGTAGCAGCAGCAGTCATCATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16752
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102322 | Nonsense | 101 | 172 | 1 | 2 |
| ENSDART00000125744 | Nonsense | 870 | 1141 | 5 | 6 |
| ENSDART00000128671 | None | None | 252 | None | 5 |
| ENSDART00000129074 | Nonsense | 718 | 966 | 7 | 9 |
| ENSDART00000134840 | None | None | 31 | None | 2 |
The following transcripts of ENSDARG00000069989 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 26164178)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 26504395 |
| GRCz11 | 1 | 27198109 |
KASP Assay ID:
2259-0642.1 (used for ordering genotyping assays)
KASP Sequence:
AGTGTCAAACTGCAYTACAAGAAKGTTCACCTAAAAGAGATGCATGTGTG[C/A]ACTGTCTCTGGATGCAATGCTGCTTTCCCCTCCAGGCGGAGCAGARATAG
Long Flanking Sequence:
GACTTTGAAAATGAGTCTGAGACATCTGAATCCAAAATGCTGTACCGCGATGAGCTGATGGACACTGACATAAATCAGACTGCTCTGGGGAAAAATATGGATAAGGAACACCAGGGGACAGAAGATGACCAACATCTAAGAAAAGATTTGGATGAACACAGCCATTCCCCACCCTCCCAACACCAGCCTGTTATCAAAATCAAAGAAGAGATCAATGATCCTACTTATGACATGTTCTGCATGGGTCAATACAGCCTTTACAATGGAGGTATGGCAGCTGCCGCTGCAGCTGCTGCCAGCATGGCTGCCTTACATGAAAGTTTCATCTCCTCTATGAGCTATGGAACAAGTACACCAAAGTTCCCCTCCCAGTCACCTGAGGGTGATCTCTGCTCTAGTCCTGATCCCAAAATCTGCTATGTCTGCAAAAAGAGCTTTAAAAGTTCCTACAGTGTCAAACTGCATTACAAGAATGTTCACCTAAAAGAGATGCATGTGTG[C/A]ACTGTCTCTGGATGCAATGCTGCTTTCCCCTCCAGGCGGAGCAGAGATAGGTGAGGCAAATCCCTTTTTATATTACAGATATATTTATAGACAATAAAAATGAATCTATTCTATACTATGCTACAATATACTACACTGTACTATACTGTTTTATGTATTTTTGTTTTAATTGTCTTTATTTAAGTGTTGCTTTAGCATAACATTTCTAAGTATGTTTCATAAAGTTTGATACAACCTTTAAGACCCTTCTGAAAAACTGTTTAAACTTCATTCTTTATTGCAAATTTGAGTGGGAAAAATGTTCAGAAAAGATGTTAACAAATTATGTTTTAACAGGAAGAACATGTGTTGATTGTACATTTCTACAGACACTTATTTAATGCAATAATTTGCTGTTTATCTATACTTGCTCACATGTCACACGCAGGTAGACATGCATACATTATCAGGGGTTCAACCTTGTCAAACCGCTGCATTCATTAGCGCATCAGGAGGTGCAG
Associated Phenotype:
Not determined