ZMP
zgc:101706
Ensembl ID:
ZFIN ID:
Description:
BRO1 domain-containing protein BROX [Source:UniProtKB/Swiss-Prot;Acc:A3KQV2]
Human Orthologue:
C1orf58
Human Description:
chromosome 1 open reading frame 58 [Source:HGNC Symbol;Acc:26512]
Mouse Orthologue:
0610010K06Rik
Mouse Description:
RIKEN cDNA 0610010K06 gene Gene [Source:MGI Symbol;Acc:MGI:1918928]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17983 | Essential Splice Site | Available for shipment | Available now |
| sa10229 | Essential Splice Site | Available for shipment | Available now |
| sa43546 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17983
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004092 | Essential Splice Site | 102 | 411 | 5 | 14 |
| ENSDART00000147044 | Essential Splice Site | 102 | 411 | 5 | 13 |
| ENSDART00000004092 | Essential Splice Site | 102 | 411 | 5 | 14 |
| ENSDART00000147044 | Essential Splice Site | 102 | 411 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 52059403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 51908641 |
| GRCz11 | 20 | 51720546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGATAAATTGAATAAAAATGAATARAANTGGMAACTGTGTGTGTTTCA[G/T]TGCGCAGCAGGATGCCGTGTTTGAGCTGGTGTCTATGGCCTTTAATGTGG
Long Flanking Sequence:
CTCTCTGTAATACACCTCCTCGTCTGATATTGACATGTGGCTTATTCTGGTTTTGTTGATTTGCATTTATTTTTCTCAGAGGCTCGGTGTTGTTGTTTTGTCTGTGGTGTTGAAATGTTTTCTGAATGTGCACAGGTTTCATTTTACCGCTTGATGGCACTACGCAAGAGAACAAGCTCAGATTCATCCAGAATTTCAAATGGACCGACACTTTACAGGGAAATATAGCCAGGTAACTCAGACAGAGTTGGTTTTATTGTTTAGCTCAGTGTTTTTTTGTTGCTGGTTTCATATTAGAACGCAAAAGGAAACAAATTGGTGAGCTGGTCTTTATTTCTGATGCATTTTAGGTGTATTTGAATGCAATGGTTGTATTGAAATGTACCTTAAGCTAGAATGCATTTTATCATTGCGTACATAAGTAGCATTAACAAAAACTATTACAATGTTTGAAGATAAATTGAATAAAAATGAATAGAATGGCAACTGTGTGTGTTTCA[G/T]TGCGCAGCAGGATGCCGTGTTTGAGCTGGTGTCTATGGCCTTTAATGTGGCCCTGTGGTACACCAAGTTTGCCTCTCGATTGGCTGGAAAGGAGAAGTAAGTTTTATGATTTATTATGATCAGATTTAGCTTTGTAAACCCTCTCTAAGTAGTTGTGTACAGCTCAGAGGTCTCATTTATATAACTTTGCATAGAAACCTTCCTAAAAGGGAATGTATGCTGTGCTAAAGATGTATTTTATTTTATTAAGGATCGTTTAAAGTGTTTCAGTTAAGTTTATATTGAAGTTTAATATGTTTACTTGGAGTTTAGTTACAGCTGTGCAAATTAGCGCAATTAGACAAAAGTCTTGTCGTCAATCCCAGTTGTAAGAGCTACAAATAATAACTCGACTTCTAGTTGATCATTTGGAAGTGGCAGAAAGTGGATTTTTGCATCACAAATACTACTGGAACCCACATGGAGCCAAGATCGTCATAGAAATAAGTCAAGTTTGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10229
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004092 | Essential Splice Site | 102 | 411 | 5 | 14 |
| ENSDART00000147044 | Essential Splice Site | 102 | 411 | 5 | 13 |
| ENSDART00000004092 | Essential Splice Site | 102 | 411 | 5 | 14 |
| ENSDART00000147044 | Essential Splice Site | 102 | 411 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 52059403)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 51908641 |
| GRCz11 | 20 | 51720546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGATAAATTGAATAAAAATGAATARAATGGMAACTGTGTGTGTTTCA[G/T]TGCGCAGCAGGATGCCGTGTTTGAGCTGGTGTCTATGGCCTTTAATGTGG
Long Flanking Sequence:
CTCTCTGTAATACACCTCCTCGTCTGATATTGACATGTGGCTTATTCTGGTTTTGTTGATTTGCATTTATTTTTCTCAGAGGCTCGGTGTTGTTGTTTTGTCTGTGGTGTTGAAATGTTTTCTGAATGTGCACAGGTTTCATTTTACCGCTTGATGGCACTACGCAAGAGAACAAGCTCAGATTCATCCAGAATTTCAAATGGACCGACACTTTACAGGGAAATATAGCCAGGTAACTCAGACAGAGTTGGTTTTATTGTTTAGCTCAGTGTTTTTTTGTTGCTGGTTTCATATTAGAACGCAAAAGGAAACAAATTGGTGAGCTGGTCTTTATTTCTGATGCATTTTAGGTGTATTTGAATGCAATGGTTGTATTGAAATGTACCTTAAGCTAGAATGCATTTTATCATTGCGTACATAAGTAGCATTAACAAAAACTATTACAATGTTTGAAGATAAATTGAATAAAAATGAATAGAATGGCAACTGTGTGTGTTTCA[G/T]TGCGCAGCAGGATGCCGTGTTTGAGCTGGTGTCTATGGCCTTTAATGTGGCCCTGTGGTACACCAAGTTTGCCTCTCGATTGGCTGGAAAGGAGAAGTAAGTTTTATGATTTATTATGATCAGATTTAGCTTTGTAAACCCTCTCTAAGTAGTTGTGTACAGCTCAGAGGTCTCATTTATATAACTTTGCATAGAAACCTTCCTAAAAGGGAATGTATGCTGTGCTAAAGATGTATTTTATTTTATTAAGGATCGTTTAAAGTGTTTCAGTTAAGTTTATATTGAAGTTTAATATGTTTACTTGGAGTTTAGTTACAGCTGTGCAAATTAGCGCAATTAGACAAAAGTCTTGTCGTCAATCCCAGTTGTAAGAGCTACAAATAATAACTCGACTTCTAGTTGATCATTTGGAAGTGGCAGAAAGTGGATTTTTGCATCACAAATACTACTGGAACCCACATGGAGCCAAGATCGTCATAGAAATAAGTCAAGTTTGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43546
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 |
|---|---|---|---|---|---|
| ENSDART00000004092 | Essential Splice Site | 224 | 411 | 8 | 14 |
| ENSDART00000147044 | Essential Splice Site | 224 | 411 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 52051909)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 51901147 |
| GRCz11 | 20 | 51713052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATTGCAGCGCTGGCCTTCGAGACTGCCAACTTCTACCAGAAAGCCGG[T/C]GAGTTTTACTTTAATAATATATTAATTAAGAATTTAATCTATTATTAATT
Long Flanking Sequence:
AATGCTGTCTGGAATGTCCTTATGGCGGGAAACTCTGGAAGGCATTGAGCTGTGTGGTTATTTCTCTCTCATTAATTTGAGCAAAATACTTAGGATTCACCAATAGTAGATTCATTATGTGTCAACTCGGTTACTGTGATATTTCAGTCAATTTCTCATTCACTCTTTAAACAAAGTTTACCAGCAGTAAATAACAGACCAGCAGTAAATAACAGAGTCCAATATTTTCACATCACATTTATTTAAGCATTTTGCATTATTTTACATTAATAATTGATTCAGTTTGCTTTATATTATACTTGCGTTGTATATCAATCAATTTTAAGGAAAACTAATTTAAAATGCTTAAAACTGAGTCTGTGTGGGTGTCTTTGTTTGTGTTTGTGTGTTTGTGTACGCGGGTTTTCAGTGACCATCGCCAGAGCCATTGAGCTGAAGCACAATGCCTCCCTCATTGCAGCGCTGGCCTTCGAGACTGCCAACTTCTACCAGAAAGCCGG[T/C]GAGTTTTACTTTAATAATATATTAATTAAGAATTTAATCTATTATTAATTATAATTATTATTAATATATACATTTTATATATTCATAATAATAATAAATAATATATTCATTATATCATAGCTAATATATTATGATTAATACTGTTATTCACAAAGGACACGTGAAATTAAAAGTGACAGTATAATGACATTTGTAGTGTTCCAAAAGATTATTCAAAGTTAATTTGATTTATTTTTGTACTGTTAATTCATTAAATATTAGTTAAAGCTGAAGTACTACAATCTCTCAAACTGAAGTCAAAATAATACAAATATTTTAAAATGGAATAGAAACATACGTCAACTACACTAACCGGCCACTTTATTAGGTATACCTTACTAGTATCAGGTTGGACCCACTTTTGCCTTCAGAACTGCTTTAATCCTTCATGAGATTCAACAAGGTACTGGAGATTTTGCTGTTGCTGTAGATTTGTCAGTTGCACATCTATGATGTGAATC
Associated Phenotype:
Not determined