ZMP
bmp1b
Ensembl ID:
ZFIN ID:
Description:
bone morphogenetic protein 1b [Source:RefSeq peptide;Acc:NP_001034901]
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 |
---|---|---|---|
sa41729 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31800 | Nonsense | Available for shipment | Available now |
sa948 | Nonsense | F2 line generated | Not yet available |
sa8469 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27675 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31799 | Essential Splice Site | Available for shipment | Available now |
sa11102 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41729
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 |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 131 | 969 | 4 | 20 |
ENSDART00000134295 | Nonsense | 131 | 261 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42288543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 41001252 |
GRCz11 | 10 | 40922438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCCCTCAGCTTTTTTACTGATTAAAACCAAACTGTTGCAGGCAGCCAG[C/T]GAGCCATTTTCAAGCAAGCCATGCGTCACTGGGAGAAACACACTTGCGTG
Long Flanking Sequence:
CATCTGACCAGTGAGAGCAATGTAGAGCCATTAGACCAATCAAAACCAAATGAGCCATGTGACCAATCAGAGCAATGTAATGCCATCTAGCAAGTGGGGTCATGTGACCAATCAAAGCAGAGTAGAGCCATTTGACCAATCAAAAAAATTTAGGCCATCTGACCAGTCAAATAAGGGTCATTAGGCTAATCAAAACCAAATGGGTCATGTGACCAATCAGAATAGTGCGAGCAGGATGCTGGATTTTAAATTAAAATAAACCAAAATGTGATTTTGACCTTGGATTAGGAAAGTTTAAACTGCGTAATGGGGCACTCTAGTGTTATTTTCCAGCTACGCTCAATCTAACACTAATCCTAAATCAGTTCAGAGCTCAGTGGCTTCCTTAAAATCATATTACCTTTGGGATGTTTCATTAGTAAGCTGGCTTTCTGGCTCAGTGTTATCCAGACGCCCTCAGCTTTTTTACTGATTAAAACCAAACTGTTGCAGGCAGCCAG[C/T]GAGCCATTTTCAAGCAAGCCATGCGTCACTGGGAGAAACACACTTGCGTGACCTTTGTGGAGAGAAGTGTGGAGGAGAGCTACATCGTCTTTACCCTCCGCCCATGTGGGTACGTTCACCATCTCCATATTGATCGCTCCGGTCTCTGATGCACAGATGCACAGCTCACCAGCAGCATTCAGAAAACTTATCTTGCTTGGCTTTCTATAGGCACAAACAGGTTTTTGTCTAGAGCAAATCTGTCTCTCTGCAGGTAGTCCAGTGAATCTGATTGCTCGGCGCTGCTCTTTTTCCTGGCATTCTTTCTGCTTGTATTATTGTACATTTTCTTTTAAGTCATCAGGAAATGACCTTCTTTTTGTATGTTATTCAATGGGAAAAATGTAGGGTGGGACTTGAGGAAGCAGAAATCGGTCTACTCTGTATTTGCGGTCTGAAATAACTTGGCTATTGGTTACTCAGTTTTATTCGTTTATGTTTAAAATGCATTATTTTAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31800
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 386 | 969 | 10 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42254376)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40967085 |
GRCz11 | 10 | 40888271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGTTTGTTGCATTTGCTTTAGGCCGCATATGTGGAGATCAGCTCCCT[G/T]AGGCCATCGTGTCCACAGACAGCGAACTGTGGATTGAGTTTCGCAGCACC
Long Flanking Sequence:
CCAGCCTGACCAGCTAAGACCAGGCTGGATATGGCTGGAAACCAGCCTGGAAATGGCCAAAACACCTCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAACCTGGATTTTTCAGCGGGGATAATGGATCAGTATGTTGCTAGTATGAATCGGTTTGTTGTTAATATGTTCAATCTAAAGTCAATGGCAGTTTTTTACAATGGAAGTCAATGGGACATTTGCTAGGATGCCGTCAGTGGTTGCTAGGGGGTGGCTAGTAAGTTGAAAGGTCATCAGAAAGCCACCATAATAATATTTATTGTACTCTCACTTACACTGCTCTCTAAATTGACCCAACAATGATGACTTATGCCGGGAAAAGTGAAAAGGCTCCACTTTAGCTTGAAGGTTATTAAAAACACTGTCACAGAATAGTTGAATATTTCATCAGTCCTGCACATGATGTCCTTTGATCAGTTTGTTGCATTTGCTTTAGGCCGCATATGTGGAGATCAGCTCCCT[G/T]AGGCCATCGTGTCCACAGACAGCGAACTGTGGATTGAGTTTCGCAGCACCAGTAATTGGGTGGGGAAAGGCTTCTCTGCCGTCTATGAAGGTAAATCTCCAGCTGAGAGCTTTCTGTTCCCATCTGAACTCATGGAGGGTTAATATTGTGATGTTCTGTACCCTGTTTCAGCAATTTGTGGAGGCGAAGTGAGACGAGACAGCGGACAGATCGAATCTCCAAATTACCCTGATGACTATCGGCCAAATAAAGCGTGCATATGGAAGATTGTGGTACCTGAGGGGTTTCACGTGGGCCTTGTCTTTCAGTCATTTGAGGTAAAGTGCAGTGTTATTTTTCATGTGTTACTCTATAACTGGCCTCAGACACTGCAAGTAAGCATCTGAGGTCAAAAAAATGTGTACATTACCTGACAAAAATTATGTCGTCGATCTCAGTTGTCAGAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTGGAAAAGTGGCAGAAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa948
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 428 | 969 | 11 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42254169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40966878 |
GRCz11 | 10 | 40888064 |
KASP Assay ID:
554-0853.1 (used for ordering genotyping assays)
KASP Sequence:
TGTACCCTGTTTCAGCAATTTGYGGAGGCGAAGTGAGACGAGACAGCGGA[C/T]AGATCGAATCTCCAAATTACCCTGATGACTATCGGCCAAATAAAGCGTGC
Long Flanking Sequence:
AATGGGACATTTGCTAGGATGCCGTCAGTGGTTGCTAGGGGGTGGCTAGTAAGTTGAAAGGTCATCAGAAAGCCACCATAATAATATTTATTGTACTCTCACTTACACTGCTCTCTAAATTGACCCAACAATGATGACTTATGCCGGGAAAAGTGAAAAGGCTCCACTTTAGCTTGAAGGTTATTAAAAACACTGTCACAGAATAGTTGAATATTTCATCAGTCCTGCACATGATGTCCTTTGATCAGTTTGTTGCATTTGCTTTAGGCCGCATATGTGGAGATCAGCTCCCTGAGGCCATCGTGTCCACAGACAGCGAACTGTGGATTGAGTTTCGCAGCACCAGTAATTGGGTGGGGAAAGGCTTCTCTGCCGTCTATGAAGGTAAATCTCCAGCTGAGAGCTTTCTGTTCCCATCTGAACTCATGGAGGGTTAATATTGTGATGTTCTGTACCCTGTTTCAGCAATTTGTGGAGGCGAAGTGAGACGAGACAGCGGA[C/T]AGATCGAATCTCCAAATTACCCTGATGACTATCGGCCAAATAAAGCGTGCATATGGAAGATTGTGGTACCTGAGGGGTTTCACGTGGGCCTTGTCTTTCAGTCATTTGAGGTAAAGTGCAGTGTTATTTTTCATGTGTTACTCTATAACTGGCCTCAGACACTGCAAGTAAGCATCTGAGGTCAAAAAAATGTGTACATTACCTGACAAAAATTATGTCGTCGATCTCAGTTGTCAGAGCAACAAATAATAACTTGACTTCTAGTTGATCATTTGGAAAAGTGGCAGAAGGTCGACTTTTCTGATGAATTATCTGTTGAGCTGCATCCCAATCATCACAGATACTGCAGAAGACTTTACATTCATTACATTTTTAATTTGAGTTTGCGTTTGGAACGACTTCACATTTTATGGAAGACATCATCCATAGTAACGGTCCCTAAGAAACCTAACGCTACTGAGTTCTCTCATTATAGACCAATAGCCCTAACAGCCCAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8469
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 555 | 969 | 13 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42249533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40962242 |
GRCz11 | 10 | 40883428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCTCACTGTGAGCAGCGCTGCATCAACAMACTGGGCAGCTTCCACTG[C/A]GCCTGCGACCCTGGCTTTGAGCTCGCCCCGGACAGAMGGAGCTGCGCAGG
Long Flanking Sequence:
ATCATGTTGAATTTTCGAATTAGCTTTGAGTGTTTTTAAATAGTTTTTTTAATTTGCGAATTGGATTTTTGATTTTTTTAATCGGTTTTTGAATTTTGGATTTGTATTTGTGTATTTTTAATTGTTTTTTGAATTTACGAAATGGATTTGTGTATTTTTGTAATGTACTTTGAATTTACAAATTGGATTTGTGTAGTTTTGCATTGTGTTTTAAGTTCACGAATTGGTCATGCGCATTTATGAATCGTGTTTTGAACTAACAAATTGGATTTAGTAAATGTGAATTGTGTTGTGGATGTATGAACTTTATTTTGTAAATGTAATATTTTTAAGACTGATCTGGCTCCATACTTGTGAACTGCATGATGTGACTGCATTGGATGCTGCATGATCTTCAAAGTCTGATTGTGTGTTTGTAATGCAGAGATTGACGAATGCTCCAGGCCTGATAATGCTCACTGTGAGCAGCGCTGCATCAACACACTGGGCAGCTTCCACTG[C/A]GCCTGCGACCCTGGCTTTGAGCTCGCCCCGGACAGACGGAGCTGCGCAGGTGATACTGATGATACCTGTTCATTCAAAACCACATGCGTCAAACTCAATGTCTGTGGGCCAAATCTGACTCACCATATCATTTTATGTGGCCCACATGAGCATATGATTCACATCAAATTTAAGTTTAAAGGGTCATGAAACAACCTTGTCTCAGCAAGGAGTTTTTACACCTCTGATTTAAAAAGCTAGGAAAAGGGGTCTTTCTAGCGGTGTTGAAGTGTGAATGTTGTATATCGAAGGAGGGAAGGGTTTGCATGAAATAGAGAGTTACATTAGGTGCATTAAAACAGTTAATTTGCACACCGGCAATGCAAACATGCTCACGCTAAAGAGATGAAGAGTGATCCTTCTGAGAGATGGAGAGCAGCATTTACTTCTCCTCACCAGAATCACACAGTTTTACTGATTAAAGTGCAGGTACGCCTTATAAATGTGAACATGTACAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27675
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 |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 629 | 969 | 15 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42241968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40954677 |
GRCz11 | 10 | 40875863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATAGCCCCTCTTTAACTGTTGCTTGTCTGTCCACAGGTTTGTAAATA[T/A]GATTATGTTGAAGTCCACAGTGGTTTGTCGGCTGACGGAAAGCTTCACGG
Long Flanking Sequence:
TGTCACAATGTTTGCACAGACATGGAATTCACCTGATGCAGACCATGTCCGTCTTTATTATTTTACAAGTCATGTAAAATAGTTACATTTCATTCATTAATTTTCTTTTTATTCAGCATATGTTTTACGCTGCGGATGCCCTTCCAGCTGCAACCCATCACTGGGAAACATACACATTCATTCACACACACACTACAGACAATTTAGCTGACATAGTGGCATTTATGTGGGCATTTGTAGCTCCGCCCTCTTTTGAAAAAGAGCATAATCTCATTTGAATTTAAAGCGACAGTCACCAAAACAGCACGATTAAGATCGAAACCTAAAAGGAGCAGTTTCATAGAGTCATAAAACATTATTTGTGTGATATTTTGAGCTGAAACGTCACACACACACACACACAAACACTCTTTAGGTACTTATTTTTACATCTTTAAAAAAAAAATCAACATAATAGCCCCTCTTTAACTGTTGCTTGTCTGTCCACAGGTTTGTAAATA[T/A]GATTATGTTGAAGTCCACAGTGGTTTGTCGGCTGACGGAAAGCTTCACGGTAAATTCTGCGGCACAGAGAAACCGGAGGCGATCACGTCCCAGCTCAACAGCATGAGTGTTGAATTCAAATCAGACAACACCGTCTCCAAGAGAGGCTTCAAAGCGCAGTTCTTTTCTGGTGAGCATGAAAAAGACCCCCAGGTGCTGCGTTTTCTGCAATAACGCTCATGTTTTTTCATCAGCTGAATCGAGCTGCATCATATTCCCCATATAATGCAATTAATGTCAAACATGCTCAGTGTCACATTTTTGCATTGCTCCTGAAGGAGACACATGTAAGCGTTTGTATTTGCATATCACATAGTTTCAGTTTCACTTTGTGTAAAGAACCCTTTATAAGATATGTATATATACAGTCAAAGTCAAAATTATTAGACCCCATTTTTTTTTTTTTTTTTTTTTAAATATTTTTCAAATGAGGTTTAACAGAGCAAGGAAAGTTTCACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31799
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 |
---|---|---|---|---|---|
ENSDART00000059795 | Essential Splice Site | 770 | 969 | 17 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42234751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40947460 |
GRCz11 | 10 | 40868646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTTGCACATGGACCCTCTCCACCACCCCTGGACACCGCATTAAACTG[G/A]TACACACTTCAATTAACCTTACAATATGAGTGGTTAAAGACCCACTATAC
Long Flanking Sequence:
AAGTAGACTACAAAAGCAGATCATAAACAATAATCACAAATAAATGAAGGATAGTAAATAAACATAAATAAACATAAAACTTATATTAATAAGTTTAATATTTTACATTTAAATAATATAATACTTTTATAAGAGTTTTAAATAAAATATTTAAAAAATATTGCTTAAAATTAAATACAATTTAGTGTTTTTGATTGATAGTGAGACATTATAAAGATTTATAATGACAATGACAGTTGTGCAGATGCACTGTGATCCTTAAATGGAGTCTTTTAATATTATAAATGGTTGTTGCTCTGAATATGCCACAAAAGATTTCTGGGTATGTAGATCATCATTCACTTATATATGTTGTGGTTTTTGTGCTGTCAGTGGGCTGCGATCAAGCTATCACCAGTGTGTCCGGGCTCATCACAAGCCCAAACTGGCCAGATAAATACCCCAGCAAGAAGGCTTGCACATGGACCCTCTCCACCACCCCTGGACACCGCATTAAACTG[G/A]TACACACTTCAATTAACCTTACAATATGAGTGGTTAAAGACCCACTATACATGCTTTTACTCAAGACTGTTTACAATCAATCCACCAGCTCTATCTAGGGCTTTTTACACTGCACATGACCCCTGATTATCATCATTATAAACCCTGCTTTTAACCCTGGGTGATGAAGTGTTTACAGTTGTAATTTTAATTTCAGCAATTAAGGGGAAACATAGATTTTGATTATAATGGGCCCTATCATACACCCAGCGTAAAGCGTGACGCAATTGTTGTTTGCTAGTTTCAGCTTGGCGCAAGAGTCGTTTTGGCATACTGTTTAAATAGCAAATGCATTTGCGCTCATGTGCGCCCATAGGTGTTCTGGTCTAAAAAAGGAGGCGTGTTAAGGCACATTGTTGGCGCGTTGCTATTTTGAGGTCAGTAGGTATCTATAATAGTCAGTTCAATAGACCAGCTTAGAGGTCTAAAGTCCAGCGCAGAGCGCATTAGTTTTGCGCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11102
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059795 | Nonsense | 788 | 969 | 18 | 20 |
ENSDART00000134295 | None | None | 261 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 42232435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 40945144 |
GRCz11 | 10 | 40866330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCGAGGAGATTGACATGGAGGCTCATCAGGAATGTGCTTATGACCACT[T/A]GGAGATTTACGACGGACAAAATGGCAGAGCGACCAGCGTCGGCCGCTTTT
Long Flanking Sequence:
CCCATTCAAAGTGAATGGGAAGCGTTGACGCTGATTCCCCGTGCGAATGGGGCGTAACCGCAGGCCGTGACGCGAGCGCACCGCGAGTCACGTGACAAGAATTGACCGATCAGCTTCAGCTTGTATGGAATATTCGCATTTTGGTATGACTAATTTTAAATTTTCTCAGACAAACACAGTAAACACAAACACACAGTGCTTTGTACTTTTCTCCATAAATAAAACTCTTATCAGGGCAATCAGCAATGTTTTGTCAGTTAGTTTGTCAAGATCTGAGAAAACCAGTTGATGGGTTCATAGCAACCTATAATAATGTAAATGACCCTAATGACCGGTGTGAAATGTGAAGAAAGATAATTACTTAGAATTGACCCAGGGTTCAACTAGTTCAAGTGTGAGAAGCTCTTTTGTGTGTGGCGACTGATTAAAATAACACTGTCTCCTGTAGGCTTTCGAGGAGATTGACATGGAGGCTCATCAGGAATGTGCTTATGACCACT[T/A]GGAGATTTACGACGGACAAAATGGCAGAGCGACCAGCGTCGGCCGCTTTTGTGGAAGTAAAAAGCCATCGCCGGTCATTTCCAGCAGTAACACTATGTTCCTGCGGTTCTTCTCGGATAATTCAGTACAGAAAAGAGGCTTCAAGGCCTCTCATTCAGCAGGTATTTCACTCTCAGAATGCTCCTGTGTTAAAGACCCCCTAAAGTTAAAGAGCCCCTATTATTCATTATAAAAGGACATATTTTAGTTTTGGGTGTCTCCAACAACAGGCTGATGTGCGTGCAGGGGCAAAAAACACTTTCATTGTCTTGTAATATACATTTATTTTTAACTAATTATCTCAAAGACTCCCATATGATTTGTTCAGCAATTCTTCTATTCCCAAACCCCTTCTTTGCATGAGGCTAATCTGCACTGATTGATCCAATGACCCAGTCTGTTGTGACTGGTCTACTACATTCAGTGCAGGAAAGAAAGAAACGCCCACCATGGTTATGAAG
Associated Phenotype:
Not determined