ZMP
bmp1a
Ensembl ID:
ZFIN ID:
Description:
bone morphogenetic protein 1a [Source:RefSeq peptide;Acc:NP_001035126]
Human Orthologue:
BMP1
Human Description:
bone morphogenetic protein 1 [Source:HGNC Symbol;Acc:1067]
Mouse Orthologue:
Bmp1
Mouse Description:
bone morphogenetic protein 1 Gene [Source:MGI Symbol;Acc:MGI:88176]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7161 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2416 | Nonsense | Available for shipment | Available now |
sa34508 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12765 | Essential Splice Site | Available for shipment | Available now |
sa17110 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7161
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127875 | Essential Splice Site | 210 | 1013 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 8 (position 53508618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51245530 |
GRCz11 | 8 | 51235373 |
KASP Assay ID:
554-5387.1 (used for ordering genotyping assays)
KASP Sequence:
TTGATTGTGTTCTTTGSATATTAACTGTAGTGTTTATTGYGCTGTCCTCA[G/T]GTGCWGTTCATACGTGGGCCGCAGAGGAGGGGGTCCGCAGGCCATWTCCA
Long Flanking Sequence:
TTTTATTTTATTTAATTTTTCTTTATTTTATTTTATTTTATTTTATTTTATAATTAATTATTTTTTTTATTGTTTCAGTTTAATATTTTTTCATTTGAATATTTTTATTTTATTTTATTTAATGTTTTCAATTTAATTAATTTTAATGTACTCAATTTAATTTAATTAGTTTAATTTAATGTGTTCAATTAAATTTTATTATTTAGTTTTATTTATTCAGTTTAATTATATTATTTTGTATTATTTTATTTTATGTAACAAAATCGTTTTAGAGTTATGGTTTTAGTTTTTTTTTTCAAAAGAGACAAGTAAATTAAAGTATTAAATAAAGATTAAATATTAGTTGGACGATATTTACCCTGGTTGACCTAATTAATGAAAGTAGACTAATAAACAGTATTTTTTAATGTTATAAATATTCTGTCATCAATGAAATAATGAATTTTGCACTTGATTGTGTTCTTTGCATATTAACTGTAGTGTTTATTGCGCTGTCCTCA[G/T]GTGCTGTTCATACGTGGGCCGCAGAGGAGGGGGTCCGCAGGCCATATCCATCGGGAAAAACTGCGATAAGTTTGGAATTGTGGTGCATGAGCTCGGACACGTGATCGGATTCTGGCATGAGCACACGCGACCCGACAGAGACGAACACGTCAGTATCATACGAGACAACATTCAGCCAGGTAGGAGAAAAAAACTGTAGGGAAAGATCACATGATCTGTGCTCAACCCACATAATAAAACACTAAAGTGTTTATAGTAAATACTCACATTTTACAGCGGTGAAAGTCCTTTTAAAGTCCACATGAACCAGAAGCTGCAACCACTGTGATCATACCAGTCAACATTCGGATCATAAAATCCGGGAGGTTTTCTCTGGGGGTGCGCGCAAAGTGAAGAGCGGGGACGGCCTGGGGGGCGGTGGTGGGTGGTTGGTGCGCACAAACTGAGGAGCGAGGGGAAAGGTGCACGCGAAGTGAAGTGCGGGCAGCGGGTATGAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2416
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 |
---|---|---|---|---|---|
ENSDART00000127875 | Nonsense | 522 | 1013 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 8 (position 53469811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51206723 |
GRCz11 | 8 | 51196461 |
KASP Assay ID:
554-2518.1 (used for ordering genotyping assays)
KASP Sequence:
AATGCAAGATCGAGAGGCATGATAACTGTGCGTACGACTACCTGGAGGTT[C/T]GAGACGGGAACTCRGAAAGCAGCCCGCTTTTGGGCAGGTTCTGCGGTTAT
Long Flanking Sequence:
GAACTGCGCGCACTCCCTAGAGGCGTTCAAGACGTGAAAAAGCGCGCACAGCGGCCACAGCGGATTCGCGAAAACAAAAACTGCACAAATACGTACCTCCTGGGAAGTATTTCGCGGTCTCCAGAAACGCCCGCGGTGCTACATTTCCAGAATGAGCCTTTTTAATATAGCGTTTCTCTAGGAACTGTGTCACAATACAATTTGACACTTAATCTACATTGTTACTGAAATAAACGACAACAGCATTTACATATTATTCTGATGTCTCTGGGTTTAATTTAGATCATCTGTAGCCAGCTGGAGTAAAAAAGAAAGAAAGAAACGAATACGTACTATTTGAAAACAGAGTTATAGCTCTGTCATTTTACATTTTACAAATGTCATTTACATTTGTCATCTGACAGCTTTAAACTTATCTTTTCCGTTTATTCTTTCATGTTTTGTCTTTTCAATGCAAGATCGAGAGGCATGATAACTGTGCGTACGACTACCTGGAGGTT[C/T]GAGACGGGAACTCGGAAAGCAGCCCGCTTTTGGGCAGGTTCTGCGGTTATGACAAACCTGATGATATTAAATCCAGTTCCAACCAGCTCTGGATGAAATTCGTGTCTGACGGTTCTGTTAATAAGGCCGGATTTGCTGCCAATTTCTTCAAAGGTGAGCTGTCGAATTGTTTGCTGCACGCTTAGAAATTTCAGAAACGTCAATTTAACATTATTCGGAGATTTCGGGAACACGCATACAGCTGAAGTCCAAATTAATAGACATAAATTATGATGAAGCTTAAGAGTTGTTTTGTTTTAATTAAGAAAGTTATCAAAATCTTTTTTGAATTTTTTGAGCACGATGCTAATGAACTAATCCCTTTCAATGACCTATGCTAAGGTAAAAGTGCTAAAAACTCAACAGTTTAACTCTAGGTGAGCATTAAAATGAAGTTATTTCTTGAAAAAAGTGGAGTGTACCTTTAAGAAACTTGAATAAGGCACGAATTACTGCATACA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa34508
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 |
---|---|---|---|---|---|
ENSDART00000127875 | Nonsense | 646 | 1013 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 8 (position 53462479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51199391 |
GRCz11 | 8 | 51189378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTCCCGGCTGGCCCAAAGAGTACCCACCTAACAAGAACTGCATCTGG[C/T]AGCTCGTGGCGCCGACGCAGTACCGCATCACGCTGCTTTTCGACGTCTTC
Long Flanking Sequence:
TTTTATGTTAAGACAGCTGTTAGCACAGCTGTAAAGTTATGTTATAATAACATTGTAATAAAGCTGTAATAACCCCTTCCTAACAGTACCGGTTTTCAGATTGCGCCATAAAAAAAACTAAACTCATAAAACTTTGGAACCACAAGAGATTGATAGAGTTATGTTTCAGTTTTGGGCGAACCATCCCCTTAAGATTGGATAACAAGCATAGCAGATGCTGTTCTGTTATAGCTTTTGACCTAACCGTGGTCCTAATCTACCTACCATGGTTACTAAACAGATAGAATAAGGTTTTAAGCTCAGGACCTTTCTGCAGTACACCCTCTGCTCTACATCATACATTCTTGTGTAATGTTATTTTGCCTGTTTGTCTTATAGTTGTTGTTGTTTTTTTTTTTTTCCCTCCAGCTGCCTGTGGGGGTTTCATCACCAAGCTGAACGGGTCCATCACCAGTCCCGGCTGGCCCAAAGAGTACCCACCTAACAAGAACTGCATCTGG[C/T]AGCTCGTGGCGCCGACGCAGTACCGCATCACGCTGCTTTTCGACGTCTTCGAGACCGAGGGCAACGATGTGAGCACTAGGTTTTTACCACTGAGTGGGGTGGGTCTGTCTGGTTCATTTCTGCTGAATTGGTGTACATCACCACAGTGCTTTAGGGAGTGACCTCTCCAAAATGCCTTTATGTTTGCTCACCTGATTTGTAGCGGGAGCACTTTTAGCTTAGCTTAGCATAAACCATCGAATCAGATTGGACCGTTAGCATCTCGCTAATAACCGAATCATCACACACTGTAAAAAACATTTAGCTGACTTTACTTGAAAAAAAAAGACAGTAAACTCATTGCCTTATAATTATTAAGGAAACAAACTATATGCATAATTATAAAAGTTACCTTTTATAAATAAAGTTTGCTGACATTTTAAAGTAAAATCAACTTGTTGCTTGTAAAGGTAACGGGTTTATTAACTGTTTTAAAGTAAAGTAACTAATGGCTTTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12765
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127875 | Essential Splice Site | 668 | 1013 | 14 | 20 |
ENSDART00000127875 | Essential Splice Site | 668 | 1013 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 8 (position 53462410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51199322 |
GRCz11 | 8 | 51189309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTACCGCATCAMGCTGCTTTTCGACGTCTTCGAGACCGAGGGCAACGAT[G/A]TGAGCACTAGRTTTTTACCACTGAGWRGGGTGGGTCTGTCYGGTTCATTT
Long Flanking Sequence:
TAACCCCTTCCTAACAGTACCGGTTTTCAGATTGCGCCATAAAAAAAACTAAACTCATAAAACTTTGGAACCACAAGAGATTGATAGAGTTATGTTTCAGTTTTGGGCGAACCATCCCCTTAAGATTGGATAACAAGCATAGCAGATGCTGTTCTGTTATAGCTTTTGACCTAACCGTGGTCCTAATCTACCTACCATGGTTACTAAACAGATAGAATAAGGTTTTAAGCTCAGGACCTTTCTGCAGTACACCCTCTGCTCTACATCATACATTCTTGTGTAATGTTATTTTGCCTGTTTGTCTTATAGTTGTTGTTGTTTTTTTTTTTTTCCCTCCAGCTGCCTGTGGGGGTTTCATCACCAAGCTGAACGGGTCCATCACCAGTCCCGGCTGGCCCAAAGAGTACCCACCTAACAAGAACTGCATCTGGCAGCTCGTGGCGCCGACGCAGTACCGCATCACGCTGCTTTTCGACGTCTTCGAGACCGAGGGCAACGAT[G/A]TGAGCACTAGGTTTTTACCACTGAGTGGGGTGGGTCTGTCTGGTTCATTTCTGCTGAATTGGTGTACATCACCACAGTGCTTTAGGGAGTGACCTCTCCAAAATGCCTTTATGTTTGCTCACCTGATTTGTAGCGGGAGCACTTTTAGCTTAGCTTAGCATAAACCATCGAATCAGATTGGACCGTTAGCATCTCGCTAATAACCGAATCATCACACACTGTAAAAAACATTTAGCTGACTTTACTTGAAAAAAAAAGACAGTAAACTCATTGCCTTATAATTATTAAGGAAACAAACTATATGCATAATTATAAAAGTTACCTTTTATAAATAAAGTTTGCTGACATTTTAAAGTAAAATCAACTTGTTGCTTGTAAAGGTAACGGGTTTATTAACTGTTTTAAAGTAAAGTAACTAATGGCTTTTTACAGTGCAGGGTTTTAGGGTATGATTTCTCCAGATTGTCTTTATATTTGCTTATTCGATATGTAGCAGGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17110
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127875 | Essential Splice Site | 668 | 1013 | 14 | 20 |
ENSDART00000127875 | Essential Splice Site | 668 | 1013 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 8 (position 53462410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 51199322 |
GRCz11 | 8 | 51189309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTACCGCATCAMGCTGCTTTTCGACGTCTTCGAGACCGAGGGCAACGAT[G/A]TGAGCACTAGRTTTTTACCACTGAGWRGGGTGGGTCTGTCYGGTTCATTT
Long Flanking Sequence:
TAACCCCTTCCTAACAGTACCGGTTTTCAGATTGCGCCATAAAAAAAACTAAACTCATAAAACTTTGGAACCACAAGAGATTGATAGAGTTATGTTTCAGTTTTGGGCGAACCATCCCCTTAAGATTGGATAACAAGCATAGCAGATGCTGTTCTGTTATAGCTTTTGACCTAACCGTGGTCCTAATCTACCTACCATGGTTACTAAACAGATAGAATAAGGTTTTAAGCTCAGGACCTTTCTGCAGTACACCCTCTGCTCTACATCATACATTCTTGTGTAATGTTATTTTGCCTGTTTGTCTTATAGTTGTTGTTGTTTTTTTTTTTTTCCCTCCAGCTGCCTGTGGGGGTTTCATCACCAAGCTGAACGGGTCCATCACCAGTCCCGGCTGGCCCAAAGAGTACCCACCTAACAAGAACTGCATCTGGCAGCTCGTGGCGCCGACGCAGTACCGCATCACGCTGCTTTTCGACGTCTTCGAGACCGAGGGCAACGAT[G/A]TGAGCACTAGGTTTTTACCACTGAGTGGGGTGGGTCTGTCTGGTTCATTTCTGCTGAATTGGTGTACATCACCACAGTGCTTTAGGGAGTGACCTCTCCAAAATGCCTTTATGTTTGCTCACCTGATTTGTAGCGGGAGCACTTTTAGCTTAGCTTAGCATAAACCATCGAATCAGATTGGACCGTTAGCATCTCGCTAATAACCGAATCATCACACACTGTAAAAAACATTTAGCTGACTTTACTTGAAAAAAAAAGACAGTAAACTCATTGCCTTATAATTATTAAGGAAACAAACTATATGCATAATTATAAAAGTTACCTTTTATAAATAAAGTTTGCTGACATTTTAAAGTAAAATCAACTTGTTGCTTGTAAAGGTAACGGGTTTATTAACTGTTTTAAAGTAAAGTAACTAATGGCTTTTTACAGTGCAGGGTTTTAGGGTATGATTTCTCCAGATTGTCTTTATATTTGCTTATTCGATATGTAGCAGGAGC
Associated Phenotype:
Not determined