ZMP
brms1
Ensembl ID:
ZFIN ID:
Description:
breast cancer metastasis-suppressor 1 [Source:RefSeq peptide;Acc:NP_956391]
Human Orthologue:
BRMS1
Human Description:
breast cancer metastasis suppressor 1 [Source:HGNC Symbol;Acc:17262]
Mouse Orthologue:
Brms1
Mouse Description:
breast cancer metastasis-suppressor 1 Gene [Source:MGI Symbol;Acc:MGI:2388804]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34210 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21110 | Essential Splice Site, Missense | Available for shipment | Available now |
sa31610 | Essential Splice Site, Missense | Available for shipment | Available now |
sa7095 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34210
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073673 | Nonsense | 177 | 265 | 6 | 7 |
ENSDART00000073675 | Nonsense | 177 | 271 | 6 | 10 |
ENSDART00000121545 | Nonsense | 177 | 271 | 6 | 10 |
ENSDART00000126714 | Nonsense | 153 | 314 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 60884210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60103175 |
GRCz11 | 7 | 60408412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCGAGTCTGTAATAAGATGCTTGTTTCTGTAGAGTGAGAAAACCCTTT[T/A]GTTTGATGCCATGAAGACAGAACTTTTGGAGAAGATCCGCAGACTGGAGG
Long Flanking Sequence:
CCTTCTAGCTGCAAGCCAGTACTGGGAAACACCCATACCCACTTATTGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTCATACACTACGGCCAATTTAGTTTATCAATTCCCCTATAGTGCATGTGTTTGGACTGTAGGGGAAACCGTAGCACCCGGAGGAAACCCATGCTAACACGGGGAGAACTGGCCCAGCAGGGACTTGAACCAGTGACCTTCTTGCTGTCCACTGTACCTCCCATTTGAGTAATATTTCATTATGTCACATTAATTCACACTCAAACATGCACACATCACATTTATTACAATCTAGAAGCATTGCCACAGTCTCTGCCACAACAGTTGTGTTTGTGTGTTGACAGTGCAGTGATGACCCTAAATCATATCGAGTCTGTAATAAGATGCTTGTTTCTGTAGAGTGAGAAAACCCTTT[T/A]GTTTGATGCCATGAAGACAGAACTTTTGGAGAAGATCCGCAGACTGGAGGAGGACAAACAGAGCATAGACATCACCTCAGGTACATGCACACGAACACTCACACACCCACATACAAGACTGCCTGCTTATCTGAATCTGGAATCTATGATACTTTTTAATAAGATTTCTATATCTGTCTACATAATATAAAAATCTTAGTAAATTTACATACACTACCAGTCAAAAGTTTAGGATCAGTTTTTTTTCTTCTTCATGTTTTTTTAAAAGAAAATTATTTTGAAGGCAGCATTTATTAAATGTAAAATAATTGTTAAATATTTAAACAAATTTTAAATAGCTGTTTTCTTATATATAGATTCAAATGAAATTATTACTCCACACATTATTGCTTTTATTACTATTACCATTATTATTAATAATAATATTAATAATAATAATTACAATAATAATTAATGTTAGAGTGATTTCTGAAGGATCATGTGACATAGTCGTAATAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21110
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 > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073673 | Missense | 226 | 265 | 7 | 7 |
ENSDART00000073675 | Essential Splice Site | 256 | 271 | None | 10 |
ENSDART00000121545 | Essential Splice Site | 256 | 271 | None | 10 |
ENSDART00000126714 | Essential Splice Site | 232 | 314 | None | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 60887114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60106079 |
GRCz11 | 7 | 60411316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGCTAAGAGAAACTGACATACTAGAGGACTGGACAGCCATCAAGAAGG[T/C]ATTAATTATGAGTTATCAACCCTTCACTCACTGTAAAAATGTTTTATGGA
Long Flanking Sequence:
TGTCATTTAGTATCTTTCACAGACAGCTTTTTTATCTTGCAAAATAAATGTTTTAAATATTCATCTTATTTGTAATCTTTTAATTGCGCCAACTCACTTGCGAGAAGTCAAACACAGTATCTTTATGTTTGAAGGCCTGTGATTATCTCTTTGCTACCGATTTTCCGCCTTTTTGTGCTTAGGAACGGAGGATGAAAGCCAGAGTTAAAAGAGAAAGCTGATGATCAGCGTTATGATACCGATAAAACCTGATTGCTCCTGTTTGGTTTTGTCGAATAGAAACTAACCCTGTAATCATCAGTTTATTCCGCCTCCTTCATGCTACAGGCCCCTGAAGTGACATGAATTATTGTTTTGACGATTTCTGAGAAGTAAAGTGAATCTGCATGGACTTCTTTCCACTCCTGCTTTCTGAGTCTGTTCGTCTTTTTCAGGGCCATACATAGTGTATATGCTAAGAGAAACTGACATACTAGAGGACTGGACAGCCATCAAGAAGG[T/C]ATTAATTATGAGTTATCAACCCTTCACTCACTGTAAAAATGTTTTATGGATCGTGATCTTTACCTTTTCTGTCTTTCAGGCAAAAGCAGCACTGATGCCCCTGAAGAAGAAAGCAGACAGTAAGTCAATTATTAAATGGGAATATTTATTTATGTTCATCATTCAAGCTTTCCTGTCGCTTTCTGTTTTTTATGCAGCTACATTGGGAGGTCAAGGTAGTCAGATGAACCTCATTAAACTTTGAAAAAACTGAGTGCTAAAATTAACTCATTGTATATTTATTAATGAAAATCACATGCGCTGACCATCTGGGACCTTGCCTTGTGCTTAATATATTTCACCAATGAATTCTTTCTCAAAAGAACAGAACAGGTTTACAGTGCAAATTGGTGTTTCTGTATAATAGTGAACTGTACAATGTTGTACAATCATAATTCAAGGTTCATGTTTGGTTTTAAGTAGAAAAGTGTTGCATGTTTTAAATAGCGCAATCTTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31610
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 > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073673 | None | None | 265 | None | 7 |
ENSDART00000073675 | Essential Splice Site | 270 | 271 | None | 10 |
ENSDART00000121545 | Essential Splice Site | 270 | 271 | None | 10 |
ENSDART00000126714 | Missense | 246 | 314 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 60887235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60106200 |
GRCz11 | 7 | 60411437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTCAGGCAAAAGCAGCACTGATGCCCCTGAAGAAGAAAGCAGACAG[T/A]AAGTCAATTATTAAATGGGAATATTTATTTATGTTCATCATTCAAGCTTT
Long Flanking Sequence:
TTTATGTTTGAAGGCCTGTGATTATCTCTTTGCTACCGATTTTCCGCCTTTTTGTGCTTAGGAACGGAGGATGAAAGCCAGAGTTAAAAGAGAAAGCTGATGATCAGCGTTATGATACCGATAAAACCTGATTGCTCCTGTTTGGTTTTGTCGAATAGAAACTAACCCTGTAATCATCAGTTTATTCCGCCTCCTTCATGCTACAGGCCCCTGAAGTGACATGAATTATTGTTTTGACGATTTCTGAGAAGTAAAGTGAATCTGCATGGACTTCTTTCCACTCCTGCTTTCTGAGTCTGTTCGTCTTTTTCAGGGCCATACATAGTGTATATGCTAAGAGAAACTGACATACTAGAGGACTGGACAGCCATCAAGAAGGTATTAATTATGAGTTATCAACCCTTCACTCACTGTAAAAATGTTTTATGGATCGTGATCTTTACCTTTTCTGTCTTTCAGGCAAAAGCAGCACTGATGCCCCTGAAGAAGAAAGCAGACAG[T/A]AAGTCAATTATTAAATGGGAATATTTATTTATGTTCATCATTCAAGCTTTCCTGTCGCTTTCTGTTTTTTATGCAGCTACATTGGGAGGTCAAGGTAGTCAGATGAACCTCATTAAACTTTGAAAAAACTGAGTGCTAAAATTAACTCATTGTATATTTATTAATGAAAATCACATGCGCTGACCATCTGGGACCTTGCCTTGTGCTTAATATATTTCACCAATGAATTCTTTCTCAAAAGAACAGAACAGGTTTACAGTGCAAATTGGTGTTTCTGTATAATAGTGAACTGTACAATGTTGTACAATCATAATTCAAGGTTCATGTTTGGTTTTAAGTAGAAAAGTGTTGCATGTTTTAAATAGCGCAATCTTTTACTAGCATGATAAAACTGGTTGCACTTTGCTATATGCAACAGTATGGGTACTTAAGGAGTACTTGTATATAGGGCTGGGCAATAATAAGATAACAATAATTATGACAATATATATTTTTTCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7095
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073673 | None | None | 265 | None | 7 |
ENSDART00000073675 | None | None | 271 | None | 10 |
ENSDART00000121545 | None | None | 271 | None | 10 |
ENSDART00000126714 | Nonsense | 262 | 314 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 60890988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60109953 |
GRCz11 | 7 | 60415190 |
KASP Assay ID:
554-5120.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGATGAAGTTGCTTTTAAACAAGCAGATGTCTGTGCAATGTGAATTTT[G/A]GGGTCTTTTCTATAATGGAGAGAGACTCTCTAAAGACAGAACTGTTGATC
Long Flanking Sequence:
AATAAATTAGGCTTGTTTAACTACATATCTTTTATATGAAGATGGTTGTATGAATTTGTATTCATTGCATTTGTGTAGTTAAGTTAAGAGATGATGTAAGCTATGCAAAATAAATTTGCTCTGGTTGACACTGGATGTTTTTCTATTAAGTAAAACAAAAACTAAATATAATTACTAAATACAAATGTGTTCACAAAATAATAAAAACTAAATCATATATAACCAAACCATTAATGGAAACTAAAACTAAACTGAAACGTACAGCAAATTTGAAAAATGTATTGACATATTCAAAAATCCAAAACAGGTCTAGTCCAAAAACAGATCAAATGTCTCTTGGCACTCACAGCTAGTTCACACAAAGATTGTCCTGCACTCTTGATCGTATCATATTTAATCACTGTAGTATGTGTGCAGTGACAAAATGTCTTGAAAATAGAGATCATTAATGAAGATGAAGTTGCTTTTAAACAAGCAGATGTCTGTGCAATGTGAATTTT[G/A]GGGTCTTTTCTATAATGGAGAGAGACTCTCTAAAGACAGAACTGTTGATCTAGAGGTTAATAACAACATCCCAGCACAGTCACTAGAGAATAAGGCATAAGACTGCATCTGTGTTCACTTTGGCTTGTTTACAAAACTGAAATGGTCTTCTTTTTTTGTCTGTGTTTCTCTTAGGGTCGTAATAAAAGGGATCAGCACAGGAGAGGTCTGGTTCAAGCGCACAGATGGCACCAAAACCAAAATCTACATCTCTTAACTTCAGAAAGGCAAATGTGCCATACGAAAAGCTTAGAGACGATAAATTACACTCAGAGAGTGTGTGAGCCTACCCTTTAATAATTACCAAATAACACACACATTTACCAACACATTGTAAAACTGCATCTAATGCTATTCACTGGTATTGAACAGACCATAGGATGTTTATTATGTCTCCATTGACTTTTTGTCTCAGATCAATGTTGCCCTTTTTGATTAGGTTTTCCTGATGTTATTATAAA
Associated Phenotype:
Not determined