ZMP
bmpr1ba
Ensembl ID:
ZFIN ID:
Description:
bone morphogenetic protein receptor type-1B [Source:RefSeq peptide;Acc:NP_571532]
Human Orthologue:
BMPR1B
Human Description:
bone morphogenetic protein receptor, type IB [Source:HGNC Symbol;Acc:1077]
Mouse Orthologue:
Bmpr1b
Mouse Description:
bone morphogenetic protein receptor, type 1B Gene [Source:MGI Symbol;Acc:MGI:107191]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13912 | Nonsense | Available for shipment | Available now |
sa33531 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20343 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13912
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 |
---|---|---|---|---|---|
ENSDART00000027129 | Nonsense | 120 | 504 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 8836830)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGTGTGTGTGTGTGYGTGCGTGCGNNNNNNNNCGNNTGCGTGCAGGTTA[T/A]GTGGTTGGAGACATTCATCATATCGCTCTGCTCATCTCWGTGAGCGTCTG
Long Flanking Sequence:
ATTGTTATTATTATTATTATTTTATTTTTATATAGATCCTTTTTTAATTTAACTTTAAAATTAAGTTAGACTAAATTCTACAATTAACAATTGTCTTCCCTTGATACAGTGTATATTTTATTTTATGAGGCAGCCCAAAACACCCCAAACACACTAAACACACTCACACAAAGTCACACCTCTGCTTAAAAGCAAGAGATGGCATCACACACACACGCACGCACGCACACAAACACACGCGCACACACACTAACACTAACATATCCACACACACACACACACACACACACATACATACATACATATACATACACACACAAACACACACACACACACACACAAATCAGTGTTATGGTGCAGAGTTTATGTTTGACATGCAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGCGTGCGTGCGTGCAGGTTA[T/A]GTGGTTGGAGACATTCATCATATCGCTCTGCTCATCTCAGTGAGCGTCTGTAGCTTCATCCTCACCTTCATCATCATCTTCTGTTACTTCAGGTGTGTAAGTTACAGCAGAAACACAAACACACTGCCTTTACCCATAGAAATGATTATCAGTAAAGCCTCTGTCGTTTTGTACCCACAAAGTACAACCTATCACTTAGATTGTGTTGCGTTTTCAACTCATTTGTATAAATATTAATAACTTGGATGCCATTGAAATGTTACCAGAGAATTGTTACTATATAAATGTTCCTATAGGCAGATTTTGATGTAAACTCTAAAACTCTTCAAACTGACCCTGACTGCAAACTTTGAATCCACTACATTAGTTTATTTTAATATAATTTGTCTCTCAGTGATCACCATGTACACATCAGTATTATATAGTTTTGGAGTTTTAGTGTAGATTCTGTCTCATGTTTTCTGTGCCGTGTGTGTGTGTGTACATTTCAGATATAAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33531
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 |
---|---|---|---|---|---|
ENSDART00000027129 | Nonsense | 250 | 504 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 8834194)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 7013278 |
GRCz11 | 5 | 7504433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTTTCACCACAGAGGAGGCCAGCTGGTTCAGGGAGACCGAGATCTA[T/A]CAGACCGTCCTCATGAGACATGACAATATACTGGGTGAGCATAACACACT
Long Flanking Sequence:
CTATCGATGAGAAATCTTGTCGCGATTTAACCTTACGAGGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTTTGTTTGTATGTATGTATATATTTATTTTTTGTCATATTGGTTTTGTTTGTAAGTGTTTGAAAATGGGGAAAATTGTTAGCTAGTATACATTATTTTACTTAAAGTAGAAAATGTAAATATAATATAATATAATATAATATAATATAATATAATATATTTTTATAATATTAAAATATTTTTATTAAATAATTATTTATATAAAATTATAAATAATGTGTAAATGTGTGTGTAGGTGCAGCGCACTATAGCGAAGCAGATCCAGATGGTGACACAGATCGGGAAGGGTCGCTATGGAGAAGTGTGGATGGGAAGATGGAGAGGAGAGAAAGTAGCTGTGAAAGTGTTTTTCACCACAGAGGAGGCCAGCTGGTTCAGGGAGACCGAGATCTA[T/A]CAGACCGTCCTCATGAGACATGACAATATACTGGGTGAGCATAACACACTATTACATATTTGAAGATCCAGAAAAGTTCTGTTTGTCCAGTTTTCACATTCATTCCCTTTCATAAACTTATGTCACGCTAGATAAAGAAAAAAAATAGTTTCTCTAAGAACCGTCAAATTGAAAGGCCTTATTGCAGGTTTTACCCCTGTGCCGTTGAAACAAATAATCAAACATTCATTGTTAATAAGCTTATGTTTTGTTGGCAAGACTTCAAAATTGTAACAATTTTTATTTTAAATGAAAAACTTTCCAAGTATTTTTTTCCTTGTTTTCTGCTTTTACACATTGCAGGCCAAATTAGTTAAAACACAATAATTATGTGAGTATATTGATATGAAATTTAGTTCTGTCAATGATTAATCATGATTAATTGCATCCAAAAGTTCATATTTACAAAATATATATGCGTGTACTTCTGATTTTTTTTTGTATATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20343
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 |
---|---|---|---|---|---|
ENSDART00000027129 | Nonsense | 425 | 504 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 5 (position 8824634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 7003718 |
GRCz11 | 5 | 7494873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAAGTGAGATGTTGTGTGTTGTTTGTGCAGGTATAGTAGAGGAGTA[T/A]CAGCTGCCGTATCATGATCATGTTCCCAATGACCCGTCATATGAAGACAT
Long Flanking Sequence:
AATGTGTTTGGTCATTATCAATGTACTGTCACTTTAAATGAGCGTGTGCAGCGCGTCAAAAATAGACCCGGCGCCGAAACTATCGCTGCACTGCTGCTTTGCTGACGCTCACGCCTCGCTCTGAAGCGCTGCTGCTGCGTGCTGTATGAAAGCTCTAATCTGTTAACATGGACGCCGAAAACACACGCGCCGCTGATGCTTGCGGTGTGAAACAGGCGTAAGAGCAATTTTAAATGTGGTTTTAGGATGCCAAAAACACCAAAAAACACAATTAGGATCAAAACCTAAAGGAGTCAGTTTCAAAGAGTTATAAAACATTATCAGTGTGGTATTTTGAACTGAATCTTTACATACACACTCTAAGATTATCAGAAACTGATTTTACATCTTGTAAAAAGCAGCATAATAGGTCCCCTTAAGTTTTACATAATTTGACATGTAGGAGAATTTGTCTGAAGTGAGATGTTGTGTGTTGTTTGTGCAGGTATAGTAGAGGAGTA[T/A]CAGCTGCCGTATCATGATCATGTTCCCAATGACCCGTCATATGAAGACATGAGAGAGGTGGTCTGCATCAAGAGGATACGACCCTCCTTCCCCAACCGCTGGAGCAGTGATGAGGTACGTTTTAGCTAACTACAAAAAAAATAATTATATCTATATACAGTTAGAATTATCAGCCCCCCTGTTTATTTTTTCCCCAATTTCTGTTTAACGGAGAGAAGATTTTCTAAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGGTTTATTTTATTTTTGCCGTGATGACAGTAAATAATATTTTACTAGATATTTTCCAAGACACTGCTATACAGCTTAAAGGGTCACGAAACACCAAAACACATTTTTTGAGCTGTTGACAGTCGTATATGTGTCCCACACTGCTAAAAACACTATTAGGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTTGTACTTCC
Associated Phenotype:
Not determined